TR201802596T4 - Pulsatil ilaç salımı. - Google Patents
Pulsatil ilaç salımı. Download PDFInfo
- Publication number
- TR201802596T4 TR201802596T4 TR2018/02596T TR201802596T TR201802596T4 TR 201802596 T4 TR201802596 T4 TR 201802596T4 TR 2018/02596 T TR2018/02596 T TR 2018/02596T TR 201802596 T TR201802596 T TR 201802596T TR 201802596 T4 TR201802596 T4 TR 201802596T4
- Authority
- TR
- Turkey
- Prior art keywords
- disease
- acid
- hydrochloride
- syndrome
- drugs
- Prior art date
Links
- 239000003814 drug Substances 0.000 title claims abstract description 44
- 229940079593 drug Drugs 0.000 title claims abstract description 43
- 230000000541 pulsatile effect Effects 0.000 title 1
- 239000000203 mixture Substances 0.000 claims abstract description 44
- 239000013543 active substance Substances 0.000 claims abstract description 39
- 230000003111 delayed effect Effects 0.000 claims abstract description 36
- -1 kalazine Chemical compound 0.000 claims description 62
- OKMWKBLSFKFYGZ-UHFFFAOYSA-N 1-behenoylglycerol Chemical group CCCCCCCCCCCCCCCCCCCCCC(=O)OCC(O)CO OKMWKBLSFKFYGZ-UHFFFAOYSA-N 0.000 claims description 16
- 239000001993 wax Substances 0.000 claims description 14
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 13
- 229960001475 zolpidem Drugs 0.000 claims description 11
- 201000006549 dyspepsia Diseases 0.000 claims description 10
- ZAFYATHCZYHLPB-UHFFFAOYSA-N zolpidem Chemical compound N1=C2C=CC(C)=CN2C(CC(=O)N(C)C)=C1C1=CC=C(C)C=C1 ZAFYATHCZYHLPB-UHFFFAOYSA-N 0.000 claims description 10
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 9
- 239000002253 acid Substances 0.000 claims description 8
- OROGSEYTTFOCAN-DNJOTXNNSA-N codeine Chemical compound C([C@H]1[C@H](N(CC[C@@]112)C)C3)=C[C@H](O)[C@@H]1OC1=C2C3=CC=C1OC OROGSEYTTFOCAN-DNJOTXNNSA-N 0.000 claims description 8
- 201000010099 disease Diseases 0.000 claims description 8
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 claims description 8
- JYGXADMDTFJGBT-VWUMJDOOSA-N hydrocortisone Chemical compound O=C1CC[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 JYGXADMDTFJGBT-VWUMJDOOSA-N 0.000 claims description 8
- 239000003326 hypnotic agent Substances 0.000 claims description 8
- 239000000932 sedative agent Substances 0.000 claims description 8
- HTTJABKRGRZYRN-UHFFFAOYSA-N Heparin Chemical compound OC1C(NC(=O)C)C(O)OC(COS(O)(=O)=O)C1OC1C(OS(O)(=O)=O)C(O)C(OC2C(C(OS(O)(=O)=O)C(OC3C(C(O)C(O)C(O3)C(O)=O)OS(O)(=O)=O)C(CO)O2)NS(O)(=O)=O)C(C(O)=O)O1 HTTJABKRGRZYRN-UHFFFAOYSA-N 0.000 claims description 7
- 238000000576 coating method Methods 0.000 claims description 7
- 230000001624 sedative effect Effects 0.000 claims description 7
- 208000011580 syndromic disease Diseases 0.000 claims description 7
- 208000008439 Biliary Liver Cirrhosis Diseases 0.000 claims description 6
- 208000033222 Biliary cirrhosis primary Diseases 0.000 claims description 6
- 208000015943 Coeliac disease Diseases 0.000 claims description 6
- 206010010774 Constipation Diseases 0.000 claims description 6
- 201000004624 Dermatitis Diseases 0.000 claims description 6
- ULGZDMOVFRHVEP-RWJQBGPGSA-N Erythromycin Chemical compound O([C@@H]1[C@@H](C)C(=O)O[C@@H]([C@@]([C@H](O)[C@@H](C)C(=O)[C@H](C)C[C@@](C)(O)[C@H](O[C@H]2[C@@H]([C@H](C[C@@H](C)O2)N(C)C)O)[C@H]1C)(C)O)CC)[C@H]1C[C@@](C)(OC)[C@@H](O)[C@H](C)O1 ULGZDMOVFRHVEP-RWJQBGPGSA-N 0.000 claims description 6
- 206010021518 Impaired gastric emptying Diseases 0.000 claims description 6
- FBOZXECLQNJBKD-ZDUSSCGKSA-N L-methotrexate Chemical compound C=1N=C2N=C(N)N=C(N)C2=NC=1CN(C)C1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 FBOZXECLQNJBKD-ZDUSSCGKSA-N 0.000 claims description 6
- 208000005764 Peripheral Arterial Disease Diseases 0.000 claims description 6
- 208000030831 Peripheral arterial occlusive disease Diseases 0.000 claims description 6
- 208000012654 Primary biliary cholangitis Diseases 0.000 claims description 6
- 229960000485 methotrexate Drugs 0.000 claims description 6
- BQJCRHHNABKAKU-KBQPJGBKSA-N morphine Chemical compound O([C@H]1[C@H](C=C[C@H]23)O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O BQJCRHHNABKAKU-KBQPJGBKSA-N 0.000 claims description 6
- GBBSUAFBMRNDJC-MRXNPFEDSA-N (5R)-zopiclone Chemical compound C1CN(C)CCN1C(=O)O[C@@H]1C2=NC=CN=C2C(=O)N1C1=CC=C(Cl)C=N1 GBBSUAFBMRNDJC-MRXNPFEDSA-N 0.000 claims description 5
- 108010036949 Cyclosporine Proteins 0.000 claims description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 5
- 229960004841 cefadroxil Drugs 0.000 claims description 5
- NBFNMSULHIODTC-CYJZLJNKSA-N cefadroxil monohydrate Chemical compound O.C1([C@@H](N)C(=O)N[C@H]2[C@@H]3N(C2=O)C(=C(CS3)C)C(O)=O)=CC=C(O)C=C1 NBFNMSULHIODTC-CYJZLJNKSA-N 0.000 claims description 5
- 229960001265 ciclosporin Drugs 0.000 claims description 5
- NJMYODHXAKYRHW-DVZOWYKESA-N cis-flupenthixol Chemical compound C1CN(CCO)CCN1CC\C=C\1C2=CC(C(F)(F)F)=CC=C2SC2=CC=CC=C2/1 NJMYODHXAKYRHW-DVZOWYKESA-N 0.000 claims description 5
- 229930182912 cyclosporin Natural products 0.000 claims description 5
- 208000035475 disorder Diseases 0.000 claims description 5
- FGXWKSZFVQUSTL-UHFFFAOYSA-N domperidone Chemical compound C12=CC=CC=C2NC(=O)N1CCCN(CC1)CCC1N1C2=CC=C(Cl)C=C2NC1=O FGXWKSZFVQUSTL-UHFFFAOYSA-N 0.000 claims description 5
- 229960001253 domperidone Drugs 0.000 claims description 5
- 229960002419 flupentixol Drugs 0.000 claims description 5
- 208000021302 gastroesophageal reflux disease Diseases 0.000 claims description 5
- 229920000669 heparin Polymers 0.000 claims description 5
- OROGSEYTTFOCAN-UHFFFAOYSA-N hydrocodone Natural products C1C(N(CCC234)C)C2C=CC(O)C3OC2=C4C1=CC=C2OC OROGSEYTTFOCAN-UHFFFAOYSA-N 0.000 claims description 5
- 230000000147 hypnotic effect Effects 0.000 claims description 5
- 229960005017 olanzapine Drugs 0.000 claims description 5
- KVWDHTXUZHCGIO-UHFFFAOYSA-N olanzapine Chemical compound C1CN(C)CCN1C1=NC2=CC=CC=C2NC2=C1C=C(C)S2 KVWDHTXUZHCGIO-UHFFFAOYSA-N 0.000 claims description 5
- 206010039073 rheumatoid arthritis Diseases 0.000 claims description 5
- 239000011734 sodium Substances 0.000 claims description 5
- 229910052708 sodium Inorganic materials 0.000 claims description 5
- HUNXMJYCHXQEGX-UHFFFAOYSA-N zaleplon Chemical compound CCN(C(C)=O)C1=CC=CC(C=2N3N=CC(=C3N=CC=2)C#N)=C1 HUNXMJYCHXQEGX-UHFFFAOYSA-N 0.000 claims description 5
- 229960004010 zaleplon Drugs 0.000 claims description 5
- HBOMLICNUCNMMY-XLPZGREQSA-N zidovudine Chemical compound O=C1NC(=O)C(C)=CN1[C@@H]1O[C@H](CO)[C@@H](N=[N+]=[N-])C1 HBOMLICNUCNMMY-XLPZGREQSA-N 0.000 claims description 5
- 229960000820 zopiclone Drugs 0.000 claims description 5
- KWGRBVOPPLSCSI-WPRPVWTQSA-N (-)-ephedrine Chemical compound CN[C@@H](C)[C@H](O)C1=CC=CC=C1 KWGRBVOPPLSCSI-WPRPVWTQSA-N 0.000 claims description 4
- YFGHCGITMMYXAQ-UHFFFAOYSA-N 2-[(diphenylmethyl)sulfinyl]acetamide Chemical compound C=1C=CC=CC=1C(S(=O)CC(=O)N)C1=CC=CC=C1 YFGHCGITMMYXAQ-UHFFFAOYSA-N 0.000 claims description 4
- 208000026872 Addison Disease Diseases 0.000 claims description 4
- 206010002383 Angina Pectoris Diseases 0.000 claims description 4
- 206010004446 Benign prostatic hyperplasia Diseases 0.000 claims description 4
- 239000004072 C09CA03 - Valsartan Substances 0.000 claims description 4
- 206010008609 Cholangitis sclerosing Diseases 0.000 claims description 4
- 208000014311 Cushing syndrome Diseases 0.000 claims description 4
- 208000001640 Fibromyalgia Diseases 0.000 claims description 4
- 208000007882 Gastritis Diseases 0.000 claims description 4
- 206010018364 Glomerulonephritis Diseases 0.000 claims description 4
- RPTUSVTUFVMDQK-UHFFFAOYSA-N Hidralazin Chemical compound C1=CC=C2C(NN)=NN=CC2=C1 RPTUSVTUFVMDQK-UHFFFAOYSA-N 0.000 claims description 4
- 206010020772 Hypertension Diseases 0.000 claims description 4
- 206010061218 Inflammation Diseases 0.000 claims description 4
- 208000003456 Juvenile Arthritis Diseases 0.000 claims description 4
- 206010059176 Juvenile idiopathic arthritis Diseases 0.000 claims description 4
- 208000002193 Pain Diseases 0.000 claims description 4
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims description 4
- 208000004403 Prostatic Hyperplasia Diseases 0.000 claims description 4
- 102000007327 Protamines Human genes 0.000 claims description 4
- 108010007568 Protamines Proteins 0.000 claims description 4
- LOUPRKONTZGTKE-WZBLMQSHSA-N Quinine Chemical compound C([C@H]([C@H](C1)C=C)C2)C[N@@]1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OC)C=C21 LOUPRKONTZGTKE-WZBLMQSHSA-N 0.000 claims description 4
- 208000002474 Tinea Diseases 0.000 claims description 4
- HJLSLZFTEKNLFI-UHFFFAOYSA-N Tinidazole Chemical compound CCS(=O)(=O)CCN1C(C)=NC=C1[N+]([O-])=O HJLSLZFTEKNLFI-UHFFFAOYSA-N 0.000 claims description 4
- 208000025865 Ulcer Diseases 0.000 claims description 4
- RJURFGZVJUQBHK-UHFFFAOYSA-N actinomycin D Natural products CC1OC(=O)C(C(C)C)N(C)C(=O)CN(C)C(=O)C2CCCN2C(=O)C(C(C)C)NC(=O)C1NC(=O)C1=C(N)C(=O)C(C)=C2OC(C(C)=CC=C3C(=O)NC4C(=O)NC(C(N5CCCC5C(=O)N(C)CC(=O)N(C)C(C(C)C)C(=O)OC4C)=O)C(C)C)=C3N=C21 RJURFGZVJUQBHK-UHFFFAOYSA-N 0.000 claims description 4
- 229960003805 amantadine Drugs 0.000 claims description 4
- DKNWSYNQZKUICI-UHFFFAOYSA-N amantadine Chemical compound C1C(C2)CC3CC2CC1(N)C3 DKNWSYNQZKUICI-UHFFFAOYSA-N 0.000 claims description 4
- 206010002026 amyotrophic lateral sclerosis Diseases 0.000 claims description 4
- 206010006451 bronchitis Diseases 0.000 claims description 4
- 208000025302 chronic primary adrenal insufficiency Diseases 0.000 claims description 4
- 239000011248 coating agent Substances 0.000 claims description 4
- 229960004126 codeine Drugs 0.000 claims description 4
- 208000029078 coronary artery disease Diseases 0.000 claims description 4
- 206010012601 diabetes mellitus Diseases 0.000 claims description 4
- GUBNMFJOJGDCEL-UHFFFAOYSA-N dicyclomine hydrochloride Chemical compound [Cl-].C1CCCCC1C1(C(=O)OCC[NH+](CC)CC)CCCCC1 GUBNMFJOJGDCEL-UHFFFAOYSA-N 0.000 claims description 4
- 239000002934 diuretic Substances 0.000 claims description 4
- 229940030606 diuretics Drugs 0.000 claims description 4
- ADEBPBSSDYVVLD-UHFFFAOYSA-N donepezil Chemical compound O=C1C=2C=C(OC)C(OC)=CC=2CC1CC(CC1)CCN1CC1=CC=CC=C1 ADEBPBSSDYVVLD-UHFFFAOYSA-N 0.000 claims description 4
- ASUTZQLVASHGKV-JDFRZJQESA-N galanthamine Chemical compound O1C(=C23)C(OC)=CC=C2CN(C)CC[C@]23[C@@H]1C[C@@H](O)C=C2 ASUTZQLVASHGKV-JDFRZJQESA-N 0.000 claims description 4
- 208000001288 gastroparesis Diseases 0.000 claims description 4
- 229960003878 haloperidol Drugs 0.000 claims description 4
- 208000024798 heartburn Diseases 0.000 claims description 4
- 229960000890 hydrocortisone Drugs 0.000 claims description 4
- 230000004054 inflammatory process Effects 0.000 claims description 4
- 201000002215 juvenile rheumatoid arthritis Diseases 0.000 claims description 4
- 229940031703 low substituted hydroxypropyl cellulose Drugs 0.000 claims description 4
- 229960001428 mercaptopurine Drugs 0.000 claims description 4
- GLVAUDGFNGKCSF-UHFFFAOYSA-N mercaptopurine Chemical compound S=C1NC=NC2=C1NC=N2 GLVAUDGFNGKCSF-UHFFFAOYSA-N 0.000 claims description 4
- 229960001165 modafinil Drugs 0.000 claims description 4
- HYAFETHFCAUJAY-UHFFFAOYSA-N pioglitazone Chemical compound N1=CC(CC)=CC=C1CCOC(C=C1)=CC=C1CC1C(=O)NC(=O)S1 HYAFETHFCAUJAY-UHFFFAOYSA-N 0.000 claims description 4
- 201000009395 primary hyperaldosteronism Diseases 0.000 claims description 4
- 201000000742 primary sclerosing cholangitis Diseases 0.000 claims description 4
- 208000010157 sclerosing cholangitis Diseases 0.000 claims description 4
- BNRNXUUZRGQAQC-UHFFFAOYSA-N sildenafil Chemical compound CCCC1=NN(C)C(C(N2)=O)=C1N=C2C(C(=CC=1)OCC)=CC=1S(=O)(=O)N1CCN(C)CC1 BNRNXUUZRGQAQC-UHFFFAOYSA-N 0.000 claims description 4
- 201000009890 sinusitis Diseases 0.000 claims description 4
- UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 claims description 4
- RMMXLENWKUUMAY-UHFFFAOYSA-N telmisartan Chemical compound CCCC1=NC2=C(C)C=C(C=3N(C4=CC=CC=C4N=3)C)C=C2N1CC(C=C1)=CC=C1C1=CC=CC=C1C(O)=O RMMXLENWKUUMAY-UHFFFAOYSA-N 0.000 claims description 4
- 229960005053 tinidazole Drugs 0.000 claims description 4
- 231100000397 ulcer Toxicity 0.000 claims description 4
- 229960004699 valsartan Drugs 0.000 claims description 4
- SJSNUMAYCRRIOM-QFIPXVFZSA-N valsartan Chemical compound C1=CC(CN(C(=O)CCCC)[C@@H](C(C)C)C(O)=O)=CC=C1C1=CC=CC=C1C1=NN=N[N]1 SJSNUMAYCRRIOM-QFIPXVFZSA-N 0.000 claims description 4
- SGKRLCUYIXIAHR-AKNGSSGZSA-N (4s,4ar,5s,5ar,6r,12ar)-4-(dimethylamino)-1,5,10,11,12a-pentahydroxy-6-methyl-3,12-dioxo-4a,5,5a,6-tetrahydro-4h-tetracene-2-carboxamide Chemical compound C1=CC=C2[C@H](C)[C@@H]([C@H](O)[C@@H]3[C@](C(O)=C(C(N)=O)C(=O)[C@H]3N(C)C)(O)C3=O)C3=C(O)C2=C1O SGKRLCUYIXIAHR-AKNGSSGZSA-N 0.000 claims description 3
- METKIMKYRPQLGS-GFCCVEGCSA-N (R)-atenolol Chemical compound CC(C)NC[C@@H](O)COC1=CC=C(CC(N)=O)C=C1 METKIMKYRPQLGS-GFCCVEGCSA-N 0.000 claims description 3
- UIAGMCDKSXEBJQ-IBGZPJMESA-N 3-o-(2-methoxyethyl) 5-o-propan-2-yl (4s)-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate Chemical compound COCCOC(=O)C1=C(C)NC(C)=C(C(=O)OC(C)C)[C@H]1C1=CC=CC([N+]([O-])=O)=C1 UIAGMCDKSXEBJQ-IBGZPJMESA-N 0.000 claims description 3
- QDIYJDPBMZUZEH-UHFFFAOYSA-O 4-(1-methyl-1-piperidin-1-iumyl)-2,2-diphenylbutanamide Chemical compound C=1C=CC=CC=1C(C(N)=O)(C=1C=CC=CC=1)CC[N+]1(C)CCCCC1 QDIYJDPBMZUZEH-UHFFFAOYSA-O 0.000 claims description 3
- PLGQWYOULXPJRE-UHFFFAOYSA-N 4-(3,4-dimethoxybenzoyl)oxybutyl-ethyl-[1-(4-methoxyphenyl)propan-2-yl]azanium;chloride Chemical compound Cl.C=1C=C(OC)C=CC=1CC(C)N(CC)CCCCOC(=O)C1=CC=C(OC)C(OC)=C1 PLGQWYOULXPJRE-UHFFFAOYSA-N 0.000 claims description 3
- SUBDBMMJDZJVOS-UHFFFAOYSA-N 5-methoxy-2-{[(4-methoxy-3,5-dimethylpyridin-2-yl)methyl]sulfinyl}-1H-benzimidazole Chemical compound N=1C2=CC(OC)=CC=C2NC=1S(=O)CC1=NC=C(C)C(OC)=C1C SUBDBMMJDZJVOS-UHFFFAOYSA-N 0.000 claims description 3
- AXRYRYVKAWYZBR-UHFFFAOYSA-N Atazanavir Natural products C=1C=C(C=2N=CC=CC=2)C=CC=1CN(NC(=O)C(NC(=O)OC)C(C)(C)C)CC(O)C(NC(=O)C(NC(=O)OC)C(C)(C)C)CC1=CC=CC=C1 AXRYRYVKAWYZBR-UHFFFAOYSA-N 0.000 claims description 3
- 108010019625 Atazanavir Sulfate Proteins 0.000 claims description 3
- 239000005552 B01AC04 - Clopidogrel Substances 0.000 claims description 3
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 3
- 229920001268 Cholestyramine Polymers 0.000 claims description 3
- 206010009900 Colitis ulcerative Diseases 0.000 claims description 3
- 206010009944 Colon cancer Diseases 0.000 claims description 3
- 208000001333 Colorectal Neoplasms Diseases 0.000 claims description 3
- 206010010741 Conjunctivitis Diseases 0.000 claims description 3
- PMATZTZNYRCHOR-CGLBZJNRSA-N Cyclosporin A Chemical compound CC[C@@H]1NC(=O)[C@H]([C@H](O)[C@H](C)C\C=C\C)N(C)C(=O)[C@H](C(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](C(C)C)NC(=O)[C@H](CC(C)C)N(C)C(=O)CN(C)C1=O PMATZTZNYRCHOR-CGLBZJNRSA-N 0.000 claims description 3
- 108010032976 Enfuvirtide Proteins 0.000 claims description 3
- 208000034347 Faecal incontinence Diseases 0.000 claims description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 3
- STECJAGHUSJQJN-GAUPFVANSA-N Hyoscine Natural products C1([C@H](CO)C(=O)OC2C[C@@H]3N([C@H](C2)[C@@H]2[C@H]3O2)C)=CC=CC=C1 STECJAGHUSJQJN-GAUPFVANSA-N 0.000 claims description 3
- 229930195725 Mannitol Natural products 0.000 claims description 3
- DUGOZIWVEXMGBE-UHFFFAOYSA-N Methylphenidate Chemical compound C=1C=CC=CC=1C(C(=O)OC)C1CCCCN1 DUGOZIWVEXMGBE-UHFFFAOYSA-N 0.000 claims description 3
- STECJAGHUSJQJN-UHFFFAOYSA-N N-Methyl-scopolamin Natural products C1C(C2C3O2)N(C)C3CC1OC(=O)C(CO)C1=CC=CC=C1 STECJAGHUSJQJN-UHFFFAOYSA-N 0.000 claims description 3
- 206010051606 Necrotising colitis Diseases 0.000 claims description 3
- 206010028980 Neoplasm Diseases 0.000 claims description 3
- TUZYXOIXSAXUGO-UHFFFAOYSA-N Pravastatin Natural products C1=CC(C)C(CCC(O)CC(O)CC(O)=O)C2C(OC(=O)C(C)CC)CC(O)C=C21 TUZYXOIXSAXUGO-UHFFFAOYSA-N 0.000 claims description 3
- 208000017442 Retinal disease Diseases 0.000 claims description 3
- 206010038923 Retinopathy Diseases 0.000 claims description 3
- 208000013738 Sleep Initiation and Maintenance disease Diseases 0.000 claims description 3
- 239000000150 Sympathomimetic Substances 0.000 claims description 3
- SEQDDYPDSLOBDC-UHFFFAOYSA-N Temazepam Chemical compound N=1C(O)C(=O)N(C)C2=CC=C(Cl)C=C2C=1C1=CC=CC=C1 SEQDDYPDSLOBDC-UHFFFAOYSA-N 0.000 claims description 3
- VXFJYXUZANRPDJ-WTNASJBWSA-N Trandopril Chemical compound C([C@@H](C(=O)OCC)N[C@@H](C)C(=O)N1[C@@H](C[C@H]2CCCC[C@@H]21)C(O)=O)CC1=CC=CC=C1 VXFJYXUZANRPDJ-WTNASJBWSA-N 0.000 claims description 3
- 201000006704 Ulcerative Colitis Diseases 0.000 claims description 3
- NIJJYAXOARWZEE-UHFFFAOYSA-N Valproic acid Chemical compound CCCC(C(O)=O)CCC NIJJYAXOARWZEE-UHFFFAOYSA-N 0.000 claims description 3
- 229960004538 alprazolam Drugs 0.000 claims description 3
- VREFGVBLTWBCJP-UHFFFAOYSA-N alprazolam Chemical compound C12=CC(Cl)=CC=C2N2C(C)=NN=C2CN=C1C1=CC=CC=C1 VREFGVBLTWBCJP-UHFFFAOYSA-N 0.000 claims description 3
- 229960003036 amisulpride Drugs 0.000 claims description 3
- NTJOBXMMWNYJFB-UHFFFAOYSA-N amisulpride Chemical compound CCN1CCCC1CNC(=O)C1=CC(S(=O)(=O)CC)=C(N)C=C1OC NTJOBXMMWNYJFB-UHFFFAOYSA-N 0.000 claims description 3
- 229960000836 amitriptyline Drugs 0.000 claims description 3
- KRMDCWKBEZIMAB-UHFFFAOYSA-N amitriptyline Chemical compound C1CC2=CC=CC=C2C(=CCCN(C)C)C2=CC=CC=C21 KRMDCWKBEZIMAB-UHFFFAOYSA-N 0.000 claims description 3
- 229960003277 atazanavir Drugs 0.000 claims description 3
- AXRYRYVKAWYZBR-GASGPIRDSA-N atazanavir Chemical compound C([C@H](NC(=O)[C@@H](NC(=O)OC)C(C)(C)C)[C@@H](O)CN(CC=1C=CC(=CC=1)C=1N=CC=CC=1)NC(=O)[C@@H](NC(=O)OC)C(C)(C)C)C1=CC=CC=C1 AXRYRYVKAWYZBR-GASGPIRDSA-N 0.000 claims description 3
- 229960002274 atenolol Drugs 0.000 claims description 3
- 229960002430 atomoxetine Drugs 0.000 claims description 3
- VHGCDTVCOLNTBX-QGZVFWFLSA-N atomoxetine Chemical compound O([C@H](CCNC)C=1C=CC=CC=1)C1=CC=CC=C1C VHGCDTVCOLNTBX-QGZVFWFLSA-N 0.000 claims description 3
- 229960001736 buprenorphine Drugs 0.000 claims description 3
- RMRJXGBAOAMLHD-IHFGGWKQSA-N buprenorphine Chemical compound C([C@]12[C@H]3OC=4C(O)=CC=C(C2=4)C[C@@H]2[C@]11CC[C@]3([C@H](C1)[C@](C)(O)C(C)(C)C)OC)CN2CC1CC1 RMRJXGBAOAMLHD-IHFGGWKQSA-N 0.000 claims description 3
- 201000011510 cancer Diseases 0.000 claims description 3
- RNFNDJAIBTYOQL-UHFFFAOYSA-N chloral hydrate Chemical compound OC(O)C(Cl)(Cl)Cl RNFNDJAIBTYOQL-UHFFFAOYSA-N 0.000 claims description 3
- 229960002327 chloral hydrate Drugs 0.000 claims description 3
- 229960003120 clonazepam Drugs 0.000 claims description 3
- DGBIGWXXNGSACT-UHFFFAOYSA-N clonazepam Chemical compound C12=CC([N+](=O)[O-])=CC=C2NC(=O)CN=C1C1=CC=CC=C1Cl DGBIGWXXNGSACT-UHFFFAOYSA-N 0.000 claims description 3
- GKTWGGQPFAXNFI-HNNXBMFYSA-N clopidogrel Chemical compound C1([C@H](N2CC=3C=CSC=3CC2)C(=O)OC)=CC=CC=C1Cl GKTWGGQPFAXNFI-HNNXBMFYSA-N 0.000 claims description 3
- 229960003009 clopidogrel Drugs 0.000 claims description 3
- 229960004170 clozapine Drugs 0.000 claims description 3
- QZUDBNBUXVUHMW-UHFFFAOYSA-N clozapine Chemical compound C1CN(C)CCN1C1=NC2=CC(Cl)=CC=C2NC2=CC=CC=C12 QZUDBNBUXVUHMW-UHFFFAOYSA-N 0.000 claims description 3
- 230000001934 delay Effects 0.000 claims description 3
- 229960003722 doxycycline Drugs 0.000 claims description 3
- 229960002062 enfuvirtide Drugs 0.000 claims description 3
- PEASPLKKXBYDKL-FXEVSJAOSA-N enfuvirtide Chemical compound C([C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](C)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC=1C=CC=CC=1)C(N)=O)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(C)=O)[C@@H](C)O)[C@@H](C)CC)C1=CN=CN1 PEASPLKKXBYDKL-FXEVSJAOSA-N 0.000 claims description 3
- JRURYQJSLYLRLN-BJMVGYQFSA-N entacapone Chemical compound CCN(CC)C(=O)C(\C#N)=C\C1=CC(O)=C(O)C([N+]([O-])=O)=C1 JRURYQJSLYLRLN-BJMVGYQFSA-N 0.000 claims description 3
- 229960003337 entacapone Drugs 0.000 claims description 3
- 229960001578 eszopiclone Drugs 0.000 claims description 3
- GBBSUAFBMRNDJC-INIZCTEOSA-N eszopiclone Chemical compound C1CN(C)CCN1C(=O)O[C@H]1C2=NC=CN=C2C(=O)N1C1=CC=C(Cl)C=N1 GBBSUAFBMRNDJC-INIZCTEOSA-N 0.000 claims description 3
- 229960003219 fenpiverinium Drugs 0.000 claims description 3
- 229960002897 heparin Drugs 0.000 claims description 3
- 206010022437 insomnia Diseases 0.000 claims description 3
- 239000000594 mannitol Substances 0.000 claims description 3
- 235000010355 mannitol Nutrition 0.000 claims description 3
- 229960004710 maraviroc Drugs 0.000 claims description 3
- GSNHKUDZZFZSJB-QYOOZWMWSA-N maraviroc Chemical compound CC(C)C1=NN=C(C)N1[C@@H]1C[C@H](N2CC[C@H](NC(=O)C3CCC(F)(F)CC3)C=3C=CC=CC=3)CC[C@H]2C1 GSNHKUDZZFZSJB-QYOOZWMWSA-N 0.000 claims description 3
- 229960000536 mebeverine hydrochloride Drugs 0.000 claims description 3
- 229960001344 methylphenidate Drugs 0.000 claims description 3
- 229960005181 morphine Drugs 0.000 claims description 3
- 230000004899 motility Effects 0.000 claims description 3
- 208000004995 necrotizing enterocolitis Diseases 0.000 claims description 3
- 229960000715 nimodipine Drugs 0.000 claims description 3
- 229960000381 omeprazole Drugs 0.000 claims description 3
- 229940005483 opioid analgesics Drugs 0.000 claims description 3
- 201000006195 perinatal necrotizing enterocolitis Diseases 0.000 claims description 3
- 229960002965 pravastatin Drugs 0.000 claims description 3
- TUZYXOIXSAXUGO-PZAWKZKUSA-N pravastatin Chemical compound C1=C[C@H](C)[C@H](CC[C@@H](O)C[C@@H](O)CC(O)=O)[C@H]2[C@@H](OC(=O)[C@@H](C)CC)C[C@H](O)C=C21 TUZYXOIXSAXUGO-PZAWKZKUSA-N 0.000 claims description 3
- 229960000672 rosuvastatin Drugs 0.000 claims description 3
- BPRHUIZQVSMCRT-VEUZHWNKSA-N rosuvastatin Chemical compound CC(C)C1=NC(N(C)S(C)(=O)=O)=NC(C=2C=CC(F)=CC=2)=C1\C=C\[C@@H](O)C[C@@H](O)CC(O)=O BPRHUIZQVSMCRT-VEUZHWNKSA-N 0.000 claims description 3
- 201000000306 sarcoidosis Diseases 0.000 claims description 3
- 229960002646 scopolamine Drugs 0.000 claims description 3
- STECJAGHUSJQJN-FWXGHANASA-N scopolamine Chemical compound C1([C@@H](CO)C(=O)O[C@H]2C[C@@H]3N([C@H](C2)[C@@H]2[C@H]3O2)C)=CC=CC=C1 STECJAGHUSJQJN-FWXGHANASA-N 0.000 claims description 3
- MEZLKOACVSPNER-GFCCVEGCSA-N selegiline Chemical compound C#CCN(C)[C@H](C)CC1=CC=CC=C1 MEZLKOACVSPNER-GFCCVEGCSA-N 0.000 claims description 3
- 239000000387 serotonin 5-HT4 receptor agonist Substances 0.000 claims description 3
- 239000000021 stimulant Substances 0.000 claims description 3
- 230000001975 sympathomimetic effect Effects 0.000 claims description 3
- 229940064707 sympathomimetics Drugs 0.000 claims description 3
- 239000007916 tablet composition Substances 0.000 claims description 3
- 229960003188 temazepam Drugs 0.000 claims description 3
- MIQPIUSUKVNLNT-UHFFFAOYSA-N tolcapone Chemical compound C1=CC(C)=CC=C1C(=O)C1=CC(O)=C(O)C([N+]([O-])=O)=C1 MIQPIUSUKVNLNT-UHFFFAOYSA-N 0.000 claims description 3
- 229960004603 tolcapone Drugs 0.000 claims description 3
- 229960002051 trandolapril Drugs 0.000 claims description 3
- 229960004141 zuclopenthixol Drugs 0.000 claims description 3
- WFPIAZLQTJBIFN-DVZOWYKESA-N zuclopenthixol Chemical compound C1CN(CCO)CCN1CC\C=C\1C2=CC(Cl)=CC=C2SC2=CC=CC=C2/1 WFPIAZLQTJBIFN-DVZOWYKESA-N 0.000 claims description 3
- AHOUBRCZNHFOSL-YOEHRIQHSA-N (+)-Casbol Chemical compound C1=CC(F)=CC=C1[C@H]1[C@H](COC=2C=C3OCOC3=CC=2)CNCC1 AHOUBRCZNHFOSL-YOEHRIQHSA-N 0.000 claims description 2
- JWZZKOKVBUJMES-UHFFFAOYSA-N (+-)-Isoprenaline Chemical compound CC(C)NCC(O)C1=CC=C(O)C(O)=C1 JWZZKOKVBUJMES-UHFFFAOYSA-N 0.000 claims description 2
- HMJIYCCIJYRONP-UHFFFAOYSA-N (+-)-Isradipine Chemical compound COC(=O)C1=C(C)NC(C)=C(C(=O)OC(C)C)C1C1=CC=CC2=NON=C12 HMJIYCCIJYRONP-UHFFFAOYSA-N 0.000 claims description 2
- CEMAWMOMDPGJMB-UHFFFAOYSA-N (+-)-Oxprenolol Chemical compound CC(C)NCC(O)COC1=CC=CC=C1OCC=C CEMAWMOMDPGJMB-UHFFFAOYSA-N 0.000 claims description 2
- WYDUSKDSKCASEF-LJQANCHMSA-N (1s)-1-cyclohexyl-1-phenyl-3-pyrrolidin-1-ylpropan-1-ol Chemical compound C([C@](O)(C1CCCCC1)C=1C=CC=CC=1)CN1CCCC1 WYDUSKDSKCASEF-LJQANCHMSA-N 0.000 claims description 2
- XMAYWYJOQHXEEK-OZXSUGGESA-N (2R,4S)-ketoconazole Chemical compound C1CN(C(=O)C)CCN1C(C=C1)=CC=C1OC[C@@H]1O[C@@](CN2C=NC=C2)(C=2C(=CC(Cl)=CC=2)Cl)OC1 XMAYWYJOQHXEEK-OZXSUGGESA-N 0.000 claims description 2
- RDJGLLICXDHJDY-NSHDSACASA-N (2s)-2-(3-phenoxyphenyl)propanoic acid Chemical compound OC(=O)[C@@H](C)C1=CC=CC(OC=2C=CC=CC=2)=C1 RDJGLLICXDHJDY-NSHDSACASA-N 0.000 claims description 2
- BIDNLKIUORFRQP-XYGFDPSESA-N (2s,4s)-4-cyclohexyl-1-[2-[[(1s)-2-methyl-1-propanoyloxypropoxy]-(4-phenylbutyl)phosphoryl]acetyl]pyrrolidine-2-carboxylic acid Chemical compound C([P@@](=O)(O[C@H](OC(=O)CC)C(C)C)CC(=O)N1[C@@H](C[C@H](C1)C1CCCCC1)C(O)=O)CCCC1=CC=CC=C1 BIDNLKIUORFRQP-XYGFDPSESA-N 0.000 claims description 2
- RUDATBOHQWOJDD-UHFFFAOYSA-N (3beta,5beta,7alpha)-3,7-Dihydroxycholan-24-oic acid Natural products OC1CC2CC(O)CCC2(C)C2C1C1CCC(C(CCC(O)=O)C)C1(C)CC2 RUDATBOHQWOJDD-UHFFFAOYSA-N 0.000 claims description 2
- VCOPTHOUUNAYKQ-WBTCAYNUSA-N (3s)-3,6-diamino-n-[[(2s,5s,8e,11s,15s)-15-amino-11-[(6r)-2-amino-1,4,5,6-tetrahydropyrimidin-6-yl]-8-[(carbamoylamino)methylidene]-2-(hydroxymethyl)-3,6,9,12,16-pentaoxo-1,4,7,10,13-pentazacyclohexadec-5-yl]methyl]hexanamide;(3s)-3,6-diamino-n-[[(2s,5s,8 Chemical compound N1C(=O)\C(=C/NC(N)=O)NC(=O)[C@H](CNC(=O)C[C@@H](N)CCCN)NC(=O)[C@H](C)NC(=O)[C@@H](N)CNC(=O)[C@@H]1[C@@H]1NC(N)=NCC1.N1C(=O)\C(=C/NC(N)=O)NC(=O)[C@H](CNC(=O)C[C@@H](N)CCCN)NC(=O)[C@H](CO)NC(=O)[C@@H](N)CNC(=O)[C@@H]1[C@@H]1NC(N)=NCC1 VCOPTHOUUNAYKQ-WBTCAYNUSA-N 0.000 claims description 2
- FJIKWRGCXUCUIG-HNNXBMFYSA-N (3s)-7-chloro-5-(2-chlorophenyl)-3-hydroxy-1-methyl-3h-1,4-benzodiazepin-2-one Chemical compound O=C([C@H](O)N=1)N(C)C2=CC=C(Cl)C=C2C=1C1=CC=CC=C1Cl FJIKWRGCXUCUIG-HNNXBMFYSA-N 0.000 claims description 2
- FFTVPQUHLQBXQZ-KVUCHLLUSA-N (4s,4as,5ar,12ar)-4,7-bis(dimethylamino)-1,10,11,12a-tetrahydroxy-3,12-dioxo-4a,5,5a,6-tetrahydro-4h-tetracene-2-carboxamide Chemical compound C1C2=C(N(C)C)C=CC(O)=C2C(O)=C2[C@@H]1C[C@H]1[C@H](N(C)C)C(=O)C(C(N)=O)=C(O)[C@@]1(O)C2=O FFTVPQUHLQBXQZ-KVUCHLLUSA-N 0.000 claims description 2
- SOVUOXKZCCAWOJ-HJYUBDRYSA-N (4s,4as,5ar,12ar)-9-[[2-(tert-butylamino)acetyl]amino]-4,7-bis(dimethylamino)-1,10,11,12a-tetrahydroxy-3,12-dioxo-4a,5,5a,6-tetrahydro-4h-tetracene-2-carboxamide Chemical compound C1C2=C(N(C)C)C=C(NC(=O)CNC(C)(C)C)C(O)=C2C(O)=C2[C@@H]1C[C@H]1[C@H](N(C)C)C(=O)C(C(N)=O)=C(O)[C@@]1(O)C2=O SOVUOXKZCCAWOJ-HJYUBDRYSA-N 0.000 claims description 2
- NWXMGUDVXFXRIG-WESIUVDSSA-N (4s,4as,5as,6s,12ar)-4-(dimethylamino)-1,6,10,11,12a-pentahydroxy-6-methyl-3,12-dioxo-4,4a,5,5a-tetrahydrotetracene-2-carboxamide Chemical compound C1=CC=C2[C@](O)(C)[C@H]3C[C@H]4[C@H](N(C)C)C(=O)C(C(N)=O)=C(O)[C@@]4(O)C(=O)C3=C(O)C2=C1O NWXMGUDVXFXRIG-WESIUVDSSA-N 0.000 claims description 2
- GUXHBMASAHGULD-SEYHBJAFSA-N (4s,4as,5as,6s,12ar)-7-chloro-4-(dimethylamino)-1,6,10,11,12a-pentahydroxy-3,12-dioxo-4a,5,5a,6-tetrahydro-4h-tetracene-2-carboxamide Chemical compound C1([C@H]2O)=C(Cl)C=CC(O)=C1C(O)=C1[C@@H]2C[C@H]2[C@H](N(C)C)C(=O)C(C(N)=O)=C(O)[C@@]2(O)C1=O GUXHBMASAHGULD-SEYHBJAFSA-N 0.000 claims description 2
- WSEQXVZVJXJVFP-HXUWFJFHSA-N (R)-citalopram Chemical compound C1([C@@]2(C3=CC=C(C=C3CO2)C#N)CCCN(C)C)=CC=C(F)C=C1 WSEQXVZVJXJVFP-HXUWFJFHSA-N 0.000 claims description 2
- RTHCYVBBDHJXIQ-MRXNPFEDSA-N (R)-fluoxetine Chemical compound O([C@H](CCNC)C=1C=CC=CC=1)C1=CC=C(C(F)(F)F)C=C1 RTHCYVBBDHJXIQ-MRXNPFEDSA-N 0.000 claims description 2
- TVYLLZQTGLZFBW-ZBFHGGJFSA-N (R,R)-tramadol Chemical compound COC1=CC=CC([C@]2(O)[C@H](CCCC2)CN(C)C)=C1 TVYLLZQTGLZFBW-ZBFHGGJFSA-N 0.000 claims description 2
- BGRJTUBHPOOWDU-NSHDSACASA-N (S)-(-)-sulpiride Chemical compound CCN1CCC[C@H]1CNC(=O)C1=CC(S(N)(=O)=O)=CC=C1OC BGRJTUBHPOOWDU-NSHDSACASA-N 0.000 claims description 2
- WHTVZRBIWZFKQO-AWEZNQCLSA-N (S)-chloroquine Chemical compound ClC1=CC=C2C(N[C@@H](C)CCCN(CC)CC)=CC=NC2=C1 WHTVZRBIWZFKQO-AWEZNQCLSA-N 0.000 claims description 2
- ZEUITGRIYCTCEM-KRWDZBQOSA-N (S)-duloxetine Chemical compound C1([C@@H](OC=2C3=CC=CC=C3C=CC=2)CCNC)=CC=CS1 ZEUITGRIYCTCEM-KRWDZBQOSA-N 0.000 claims description 2
- TWBNMYSKRDRHAT-RCWTXCDDSA-N (S)-timolol hemihydrate Chemical compound O.CC(C)(C)NC[C@H](O)COC1=NSN=C1N1CCOCC1.CC(C)(C)NC[C@H](O)COC1=NSN=C1N1CCOCC1 TWBNMYSKRDRHAT-RCWTXCDDSA-N 0.000 claims description 2
- KOHIRBRYDXPAMZ-YHBROIRLSA-N (S,R,R,R)-nebivolol Chemical compound C1CC2=CC(F)=CC=C2O[C@H]1[C@H](O)CNC[C@@H](O)[C@H]1OC2=CC=C(F)C=C2CC1 KOHIRBRYDXPAMZ-YHBROIRLSA-N 0.000 claims description 2
- MPPPKRYCTPRNTB-UHFFFAOYSA-N 1-bromobutane Chemical compound CCCCBr MPPPKRYCTPRNTB-UHFFFAOYSA-N 0.000 claims description 2
- FUFLCEKSBBHCMO-UHFFFAOYSA-N 11-dehydrocorticosterone Natural products O=C1CCC2(C)C3C(=O)CC(C)(C(CC4)C(=O)CO)C4C3CCC2=C1 FUFLCEKSBBHCMO-UHFFFAOYSA-N 0.000 claims description 2
- KTHVBAZBLKXIHZ-UHFFFAOYSA-N 2,2-diphenylacetic acid (1-ethyl-3-piperidinyl) ester Chemical compound C1N(CC)CCCC1OC(=O)C(C=1C=CC=CC=1)C1=CC=CC=C1 KTHVBAZBLKXIHZ-UHFFFAOYSA-N 0.000 claims description 2
- SGTNSNPWRIOYBX-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-{[2-(3,4-dimethoxyphenyl)ethyl](methyl)amino}-2-(propan-2-yl)pentanenitrile Chemical compound C1=C(OC)C(OC)=CC=C1CCN(C)CCCC(C#N)(C(C)C)C1=CC=C(OC)C(OC)=C1 SGTNSNPWRIOYBX-UHFFFAOYSA-N 0.000 claims description 2
- ABFPKTQEQNICFT-UHFFFAOYSA-M 2-chloro-1-methylpyridin-1-ium;iodide Chemical compound [I-].C[N+]1=CC=CC=C1Cl ABFPKTQEQNICFT-UHFFFAOYSA-M 0.000 claims description 2
- PPWLAQVKIFDULF-UHFFFAOYSA-N 2-phenyl-1h-pyrrolo[2,3-b]pyridine Chemical compound N1C2=NC=CC=C2C=C1C1=CC=CC=C1 PPWLAQVKIFDULF-UHFFFAOYSA-N 0.000 claims description 2
- VYVKHNNGDFVQGA-UHFFFAOYSA-N 3,4-dimethoxybenzoic acid 4-[ethyl-[1-(4-methoxyphenyl)propan-2-yl]amino]butyl ester Chemical compound C=1C=C(OC)C=CC=1CC(C)N(CC)CCCCOC(=O)C1=CC=C(OC)C(OC)=C1 VYVKHNNGDFVQGA-UHFFFAOYSA-N 0.000 claims description 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-M 3-carboxy-2,3-dihydroxypropanoate Chemical compound OC(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-M 0.000 claims description 2
- LCTZPQRFOZKZNK-UHFFFAOYSA-N 4-(diphenylmethylene)-1,1-dimethylpiperidin-1-ium Chemical compound C1C[N+](C)(C)CCC1=C(C=1C=CC=CC=1)C1=CC=CC=C1 LCTZPQRFOZKZNK-UHFFFAOYSA-N 0.000 claims description 2
- GIYAQDDTCWHPPL-UHFFFAOYSA-N 4-amino-5-bromo-N-[2-(diethylamino)ethyl]-2-methoxybenzamide Chemical compound CCN(CC)CCNC(=O)C1=CC(Br)=C(N)C=C1OC GIYAQDDTCWHPPL-UHFFFAOYSA-N 0.000 claims description 2
- WZRJTRPJURQBRM-UHFFFAOYSA-N 4-amino-n-(5-methyl-1,2-oxazol-3-yl)benzenesulfonamide;5-[(3,4,5-trimethoxyphenyl)methyl]pyrimidine-2,4-diamine Chemical compound O1C(C)=CC(NS(=O)(=O)C=2C=CC(N)=CC=2)=N1.COC1=C(OC)C(OC)=CC(CC=2C(=NC(N)=NC=2)N)=C1 WZRJTRPJURQBRM-UHFFFAOYSA-N 0.000 claims description 2
- NMUSYJAQQFHJEW-KVTDHHQDSA-N 5-azacytidine Chemical compound O=C1N=C(N)N=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O1 NMUSYJAQQFHJEW-KVTDHHQDSA-N 0.000 claims description 2
- RZTAMFZIAATZDJ-HNNXBMFYSA-N 5-o-ethyl 3-o-methyl (4s)-4-(2,3-dichlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate Chemical compound CCOC(=O)C1=C(C)NC(C)=C(C(=O)OC)[C@@H]1C1=CC=CC(Cl)=C1Cl RZTAMFZIAATZDJ-HNNXBMFYSA-N 0.000 claims description 2
- WYWHKKSPHMUBEB-UHFFFAOYSA-N 6-Mercaptoguanine Natural products N1C(N)=NC(=S)C2=C1N=CN2 WYWHKKSPHMUBEB-UHFFFAOYSA-N 0.000 claims description 2
- KSEYRUGYKHXGFW-UHFFFAOYSA-N 6-methoxy-N-[(1-prop-2-enyl-2-pyrrolidinyl)methyl]-2H-benzotriazole-5-carboxamide Chemical compound COC1=CC2=NNN=C2C=C1C(=O)NCC1CCCN1CC=C KSEYRUGYKHXGFW-UHFFFAOYSA-N 0.000 claims description 2
- STQGQHZAVUOBTE-UHFFFAOYSA-N 7-Cyan-hept-2t-en-4,6-diinsaeure Natural products C1=2C(O)=C3C(=O)C=4C(OC)=CC=CC=4C(=O)C3=C(O)C=2CC(O)(C(C)=O)CC1OC1CC(N)C(O)C(C)O1 STQGQHZAVUOBTE-UHFFFAOYSA-N 0.000 claims description 2
- 206010063409 Acarodermatitis Diseases 0.000 claims description 2
- 208000002874 Acne Vulgaris Diseases 0.000 claims description 2
- 206010001052 Acute respiratory distress syndrome Diseases 0.000 claims description 2
- UXOWGYHJODZGMF-QORCZRPOSA-N Aliskiren Chemical compound COCCCOC1=CC(C[C@@H](C[C@H](N)[C@@H](O)C[C@@H](C(C)C)C(=O)NCC(C)(C)C(N)=O)C(C)C)=CC=C1OC UXOWGYHJODZGMF-QORCZRPOSA-N 0.000 claims description 2
- 201000004384 Alopecia Diseases 0.000 claims description 2
- 208000024827 Alzheimer disease Diseases 0.000 claims description 2
- ITPDYQOUSLNIHG-UHFFFAOYSA-N Amiodarone hydrochloride Chemical compound [Cl-].CCCCC=1OC2=CC=CC=C2C=1C(=O)C1=CC(I)=C(OCC[NH+](CC)CC)C(I)=C1 ITPDYQOUSLNIHG-UHFFFAOYSA-N 0.000 claims description 2
- 229930183010 Amphotericin Natural products 0.000 claims description 2
- QGGFZZLFKABGNL-UHFFFAOYSA-N Amphotericin A Natural products OC1C(N)C(O)C(C)OC1OC1C=CC=CC=CC=CCCC=CC=CC(C)C(O)C(C)C(C)OC(=O)CC(O)CC(O)CCC(O)C(O)CC(O)CC(O)(CC(O)C2C(O)=O)OC2C1 QGGFZZLFKABGNL-UHFFFAOYSA-N 0.000 claims description 2
- 108010064760 Anidulafungin Proteins 0.000 claims description 2
- 206010002556 Ankylosing Spondylitis Diseases 0.000 claims description 2
- WZPBZJONDBGPKJ-UHFFFAOYSA-N Antibiotic SQ 26917 Natural products O=C1N(S(O)(=O)=O)C(C)C1NC(=O)C(=NOC(C)(C)C(O)=O)C1=CSC(N)=N1 WZPBZJONDBGPKJ-UHFFFAOYSA-N 0.000 claims description 2
- BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 claims description 2
- 201000001320 Atherosclerosis Diseases 0.000 claims description 2
- 206010003645 Atopy Diseases 0.000 claims description 2
- 208000023275 Autoimmune disease Diseases 0.000 claims description 2
- 206010003827 Autoimmune hepatitis Diseases 0.000 claims description 2
- 239000005465 B01AC22 - Prasugrel Substances 0.000 claims description 2
- 208000023514 Barrett esophagus Diseases 0.000 claims description 2
- 208000023665 Barrett oesophagus Diseases 0.000 claims description 2
- 108010006654 Bleomycin Proteins 0.000 claims description 2
- 208000007257 Budd-Chiari syndrome Diseases 0.000 claims description 2
- 206010006811 Bursitis Diseases 0.000 claims description 2
- 239000002126 C01EB10 - Adenosine Substances 0.000 claims description 2
- 239000005537 C09CA07 - Telmisartan Substances 0.000 claims description 2
- 229940127291 Calcium channel antagonist Drugs 0.000 claims description 2
- GAGWJHPBXLXJQN-UORFTKCHSA-N Capecitabine Chemical compound C1=C(F)C(NC(=O)OCCCCC)=NC(=O)N1[C@H]1[C@H](O)[C@H](O)[C@@H](C)O1 GAGWJHPBXLXJQN-UORFTKCHSA-N 0.000 claims description 2
- GAGWJHPBXLXJQN-UHFFFAOYSA-N Capecitabine Natural products C1=C(F)C(NC(=O)OCCCCC)=NC(=O)N1C1C(O)C(O)C(C)O1 GAGWJHPBXLXJQN-UHFFFAOYSA-N 0.000 claims description 2
- 108010065839 Capreomycin Proteins 0.000 claims description 2
- 206010007559 Cardiac failure congestive Diseases 0.000 claims description 2
- 208000031229 Cardiomyopathies Diseases 0.000 claims description 2
- 208000024172 Cardiovascular disease Diseases 0.000 claims description 2
- 208000014882 Carotid artery disease Diseases 0.000 claims description 2
- 108010020326 Caspofungin Proteins 0.000 claims description 2
- 229930186147 Cephalosporin Natural products 0.000 claims description 2
- PCLITLDOTJTVDJ-UHFFFAOYSA-N Chlormethiazole Chemical compound CC=1N=CSC=1CCCl PCLITLDOTJTVDJ-UHFFFAOYSA-N 0.000 claims description 2
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims description 2
- 208000000094 Chronic Pain Diseases 0.000 claims description 2
- VWFCHDSQECPREK-LURJTMIESA-N Cidofovir Chemical compound NC=1C=CN(C[C@@H](CO)OCP(O)(O)=O)C(=O)N=1 VWFCHDSQECPREK-LURJTMIESA-N 0.000 claims description 2
- 235000001258 Cinchona calisaya Nutrition 0.000 claims description 2
- KPSRODZRAIWAKH-JTQLQIEISA-N Ciprofibrate Natural products C1=CC(OC(C)(C)C(O)=O)=CC=C1[C@H]1C(Cl)(Cl)C1 KPSRODZRAIWAKH-JTQLQIEISA-N 0.000 claims description 2
- PTOAARAWEBMLNO-KVQBGUIXSA-N Cladribine Chemical compound C1=NC=2C(N)=NC(Cl)=NC=2N1[C@H]1C[C@H](O)[C@@H](CO)O1 PTOAARAWEBMLNO-KVQBGUIXSA-N 0.000 claims description 2
- GJSURZIOUXUGAL-UHFFFAOYSA-N Clonidine Chemical compound ClC1=CC=CC(Cl)=C1NC1=NCCN1 GJSURZIOUXUGAL-UHFFFAOYSA-N 0.000 claims description 2
- 229920002911 Colestipol Polymers 0.000 claims description 2
- 108010078777 Colistin Proteins 0.000 claims description 2
- 208000035984 Colonic Polyps Diseases 0.000 claims description 2
- 206010010539 Congenital megacolon Diseases 0.000 claims description 2
- MFYSYFVPBJMHGN-ZPOLXVRWSA-N Cortisone Chemical compound O=C1CC[C@]2(C)[C@H]3C(=O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 MFYSYFVPBJMHGN-ZPOLXVRWSA-N 0.000 claims description 2
- MFYSYFVPBJMHGN-UHFFFAOYSA-N Cortisone Natural products O=C1CCC2(C)C3C(=O)CC(C)(C(CC4)(O)C(=O)CO)C4C3CCC2=C1 MFYSYFVPBJMHGN-UHFFFAOYSA-N 0.000 claims description 2
- 206010011219 Costochondritis Diseases 0.000 claims description 2
- 208000011231 Crohn disease Diseases 0.000 claims description 2
- 201000003883 Cystic fibrosis Diseases 0.000 claims description 2
- UHDGCWIWMRVCDJ-CCXZUQQUSA-N Cytarabine Chemical compound O=C1N=C(N)C=CN1[C@H]1[C@@H](O)[C@H](O)[C@@H](CO)O1 UHDGCWIWMRVCDJ-CCXZUQQUSA-N 0.000 claims description 2
- 108010092160 Dactinomycin Proteins 0.000 claims description 2
- MQJKPEGWNLWLTK-UHFFFAOYSA-N Dapsone Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=C1 MQJKPEGWNLWLTK-UHFFFAOYSA-N 0.000 claims description 2
- 108010013198 Daptomycin Proteins 0.000 claims description 2
- 206010012289 Dementia Diseases 0.000 claims description 2
- FMTDIUIBLCQGJB-UHFFFAOYSA-N Demethylchlortetracyclin Natural products C1C2C(O)C3=C(Cl)C=CC(O)=C3C(=O)C2=C(O)C2(O)C1C(N(C)C)C(O)=C(C(N)=O)C2=O FMTDIUIBLCQGJB-UHFFFAOYSA-N 0.000 claims description 2
- 208000007342 Diabetic Nephropathies Diseases 0.000 claims description 2
- 206010012735 Diarrhoea Diseases 0.000 claims description 2
- BXZVVICBKDXVGW-NKWVEPMBSA-N Didanosine Chemical compound O1[C@H](CO)CC[C@@H]1N1C(NC=NC2=O)=C2N=C1 BXZVVICBKDXVGW-NKWVEPMBSA-N 0.000 claims description 2
- WDJUZGPOPHTGOT-OAXVISGBSA-N Digitoxin Natural products O([C@H]1[C@@H](C)O[C@@H](O[C@@H]2C[C@@H]3[C@@](C)([C@@H]4[C@H]([C@]5(O)[C@@](C)([C@H](C6=CC(=O)OC6)CC5)CC4)CC3)CC2)C[C@H]1O)[C@H]1O[C@@H](C)[C@H](O[C@H]2O[C@@H](C)[C@@H](O)[C@@H](O)C2)[C@@H](O)C1 WDJUZGPOPHTGOT-OAXVISGBSA-N 0.000 claims description 2
- LTMHDMANZUZIPE-AMTYYWEZSA-N Digoxin Natural products O([C@H]1[C@H](C)O[C@H](O[C@@H]2C[C@@H]3[C@@](C)([C@@H]4[C@H]([C@]5(O)[C@](C)([C@H](O)C4)[C@H](C4=CC(=O)OC4)CC5)CC3)CC2)C[C@@H]1O)[C@H]1O[C@H](C)[C@@H](O[C@H]2O[C@@H](C)[C@H](O)[C@@H](O)C2)[C@@H](O)C1 LTMHDMANZUZIPE-AMTYYWEZSA-N 0.000 claims description 2
- 206010013554 Diverticulum Diseases 0.000 claims description 2
- XPOQHMRABVBWPR-UHFFFAOYSA-N Efavirenz Natural products O1C(=O)NC2=CC=C(Cl)C=C2C1(C(F)(F)F)C#CC1CC1 XPOQHMRABVBWPR-UHFFFAOYSA-N 0.000 claims description 2
- 206010014561 Emphysema Diseases 0.000 claims description 2
- XQSPYNMVSIKCOC-NTSWFWBYSA-N Emtricitabine Chemical compound C1=C(F)C(N)=NC(=O)N1[C@H]1O[C@@H](CO)SC1 XQSPYNMVSIKCOC-NTSWFWBYSA-N 0.000 claims description 2
- 108010061435 Enalapril Proteins 0.000 claims description 2
- 201000009273 Endometriosis Diseases 0.000 claims description 2
- 206010014954 Eosinophilic fasciitis Diseases 0.000 claims description 2
- 206010014989 Epidermolysis bullosa Diseases 0.000 claims description 2
- 108010056764 Eptifibatide Proteins 0.000 claims description 2
- 208000010228 Erectile Dysfunction Diseases 0.000 claims description 2
- 201000000297 Erysipelas Diseases 0.000 claims description 2
- 206010016654 Fibrosis Diseases 0.000 claims description 2
- DJBNUMBKLMJRSA-UHFFFAOYSA-N Flecainide Chemical compound FC(F)(F)COC1=CC=C(OCC(F)(F)F)C(C(=O)NCC2NCCCC2)=C1 DJBNUMBKLMJRSA-UHFFFAOYSA-N 0.000 claims description 2
- UIOFUWFRIANQPC-JKIFEVAISA-N Floxacillin Chemical compound N([C@@H]1C(N2[C@H](C(C)(C)S[C@@H]21)C(O)=O)=O)C(=O)C1=C(C)ON=C1C1=C(F)C=CC=C1Cl UIOFUWFRIANQPC-JKIFEVAISA-N 0.000 claims description 2
- 206010016936 Folliculitis Diseases 0.000 claims description 2
- IECPWNUMDGFDKC-UHFFFAOYSA-N Fusicsaeure Natural products C12C(O)CC3C(=C(CCC=C(C)C)C(O)=O)C(OC(C)=O)CC3(C)C1(C)CCC1C2(C)CCC(O)C1C IECPWNUMDGFDKC-UHFFFAOYSA-N 0.000 claims description 2
- HEMJJKBWTPKOJG-UHFFFAOYSA-N Gemfibrozil Chemical compound CC1=CC=C(C)C(OCCCC(C)(C)C(O)=O)=C1 HEMJJKBWTPKOJG-UHFFFAOYSA-N 0.000 claims description 2
- 229930182566 Gentamicin Natural products 0.000 claims description 2
- CEAZRRDELHUEMR-URQXQFDESA-N Gentamicin Chemical compound O1[C@H](C(C)NC)CC[C@@H](N)[C@H]1O[C@H]1[C@H](O)[C@@H](O[C@@H]2[C@@H]([C@@H](NC)[C@@](C)(O)CO2)O)[C@H](N)C[C@@H]1N CEAZRRDELHUEMR-URQXQFDESA-N 0.000 claims description 2
- 208000010412 Glaucoma Diseases 0.000 claims description 2
- 206010018498 Goitre Diseases 0.000 claims description 2
- 208000015023 Graves' disease Diseases 0.000 claims description 2
- 208000030836 Hashimoto thyroiditis Diseases 0.000 claims description 2
- 206010019280 Heart failures Diseases 0.000 claims description 2
- 208000018565 Hemochromatosis Diseases 0.000 claims description 2
- 206010073069 Hepatic cancer Diseases 0.000 claims description 2
- ZRYHPQCHHOKSMD-UHFFFAOYSA-N Hexocyclium Chemical compound C1C[N+](C)(C)CCN1CC(O)(C=1C=CC=CC=1)C1CCCCC1 ZRYHPQCHHOKSMD-UHFFFAOYSA-N 0.000 claims description 2
- 208000004592 Hirschsprung disease Diseases 0.000 claims description 2
- 206010020590 Hypercalciuria Diseases 0.000 claims description 2
- 208000035150 Hypercholesterolemia Diseases 0.000 claims description 2
- 208000031226 Hyperlipidaemia Diseases 0.000 claims description 2
- 206010020751 Hypersensitivity Diseases 0.000 claims description 2
- 206010020850 Hyperthyroidism Diseases 0.000 claims description 2
- 206010020944 Hypoaldosteronism Diseases 0.000 claims description 2
- 208000013016 Hypoglycemia Diseases 0.000 claims description 2
- XQFRJNBWHJMXHO-RRKCRQDMSA-N IDUR Chemical compound C1[C@H](O)[C@@H](CO)O[C@H]1N1C(=O)NC(=O)C(I)=C1 XQFRJNBWHJMXHO-RRKCRQDMSA-N 0.000 claims description 2
- HEFNNWSXXWATRW-UHFFFAOYSA-N Ibuprofen Chemical compound CC(C)CC1=CC=C(C(C)C(O)=O)C=C1 HEFNNWSXXWATRW-UHFFFAOYSA-N 0.000 claims description 2
- XDXDZDZNSLXDNA-TZNDIEGXSA-N Idarubicin Chemical compound C1[C@H](N)[C@H](O)[C@H](C)O[C@H]1O[C@@H]1C2=C(O)C(C(=O)C3=CC=CC=C3C3=O)=C3C(O)=C2C[C@@](O)(C(C)=O)C1 XDXDZDZNSLXDNA-TZNDIEGXSA-N 0.000 claims description 2
- XDXDZDZNSLXDNA-UHFFFAOYSA-N Idarubicin Natural products C1C(N)C(O)C(C)OC1OC1C2=C(O)C(C(=O)C3=CC=CC=C3C3=O)=C3C(O)=C2CC(O)(C(C)=O)C1 XDXDZDZNSLXDNA-UHFFFAOYSA-N 0.000 claims description 2
- 201000009794 Idiopathic Pulmonary Fibrosis Diseases 0.000 claims description 2
- 206010021531 Impetigo Diseases 0.000 claims description 2
- 208000029836 Inguinal Hernia Diseases 0.000 claims description 2
- 102000006992 Interferon-alpha Human genes 0.000 claims description 2
- 108010047761 Interferon-alpha Proteins 0.000 claims description 2
- 208000005615 Interstitial Cystitis Diseases 0.000 claims description 2
- DHUZAAUGHUHIDS-ONEGZZNKSA-N Isomyristicin Chemical compound COC1=CC(\C=C\C)=CC2=C1OCO2 DHUZAAUGHUHIDS-ONEGZZNKSA-N 0.000 claims description 2
- JTPUMZTWMWIVPA-UHFFFAOYSA-O Isopropamide Chemical compound C=1C=CC=CC=1C(C(N)=O)(CC[N+](C)(C(C)C)C(C)C)C1=CC=CC=C1 JTPUMZTWMWIVPA-UHFFFAOYSA-O 0.000 claims description 2
- UETNIIAIRMUTSM-UHFFFAOYSA-N Jacareubin Natural products CC1(C)OC2=CC3Oc4c(O)c(O)ccc4C(=O)C3C(=C2C=C1)O UETNIIAIRMUTSM-UHFFFAOYSA-N 0.000 claims description 2
- 208000011200 Kawasaki disease Diseases 0.000 claims description 2
- WTDRDQBEARUVNC-LURJTMIESA-N L-DOPA Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C(O)=C1 WTDRDQBEARUVNC-LURJTMIESA-N 0.000 claims description 2
- WTDRDQBEARUVNC-UHFFFAOYSA-N L-Dopa Natural products OC(=O)C(N)CC1=CC=C(O)C(O)=C1 WTDRDQBEARUVNC-UHFFFAOYSA-N 0.000 claims description 2
- WXFIGDLSSYIKKV-RCOVLWMOSA-N L-Metaraminol Chemical compound C[C@H](N)[C@H](O)C1=CC=CC(O)=C1 WXFIGDLSSYIKKV-RCOVLWMOSA-N 0.000 claims description 2
- 201000010538 Lactose Intolerance Diseases 0.000 claims description 2
- GSDSWSVVBLHKDQ-JTQLQIEISA-N Levofloxacin Chemical compound C([C@@H](N1C2=C(C(C(C(O)=O)=C1)=O)C=C1F)C)OC2=C1N1CCN(C)CC1 GSDSWSVVBLHKDQ-JTQLQIEISA-N 0.000 claims description 2
- JAQUASYNZVUNQP-USXIJHARSA-N Levorphanol Chemical compound C1C2=CC=C(O)C=C2[C@]23CCN(C)[C@H]1[C@@H]2CCCC3 JAQUASYNZVUNQP-USXIJHARSA-N 0.000 claims description 2
- 108010007859 Lisinopril Proteins 0.000 claims description 2
- 208000019693 Lung disease Diseases 0.000 claims description 2
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims description 2
- 208000001344 Macular Edema Diseases 0.000 claims description 2
- 206010025415 Macular oedema Diseases 0.000 claims description 2
- 208000010315 Mastoiditis Diseases 0.000 claims description 2
- 208000027530 Meniere disease Diseases 0.000 claims description 2
- 201000009906 Meningitis Diseases 0.000 claims description 2
- 206010027406 Mesothelioma Diseases 0.000 claims description 2
- ROAIXOJGRFKICW-UHFFFAOYSA-N Methenamine hippurate Chemical compound C1N(C2)CN3CN1CN2C3.OC(=O)CNC(=O)C1=CC=CC=C1 ROAIXOJGRFKICW-UHFFFAOYSA-N 0.000 claims description 2
- 108010021062 Micafungin Proteins 0.000 claims description 2
- ZFMITUMMTDLWHR-UHFFFAOYSA-N Minoxidil Chemical compound NC1=[N+]([O-])C(N)=CC(N2CCCCC2)=N1 ZFMITUMMTDLWHR-UHFFFAOYSA-N 0.000 claims description 2
- 229930192392 Mitomycin Natural products 0.000 claims description 2
- UWWDHYUMIORJTA-HSQYWUDLSA-N Moexipril Chemical compound C([C@@H](C(=O)OCC)N[C@@H](C)C(=O)N1[C@@H](CC2=CC(OC)=C(OC)C=C2C1)C(O)=O)CC1=CC=CC=C1 UWWDHYUMIORJTA-HSQYWUDLSA-N 0.000 claims description 2
- UCHDWCPVSPXUMX-TZIWLTJVSA-N Montelukast Chemical compound CC(C)(O)C1=CC=CC=C1CC[C@H](C=1C=C(\C=C\C=2N=C3C=C(Cl)C=CC3=CC=2)C=CC=1)SCC1(CC(O)=O)CC1 UCHDWCPVSPXUMX-TZIWLTJVSA-N 0.000 claims description 2
- 208000023178 Musculoskeletal disease Diseases 0.000 claims description 2
- 208000031888 Mycoses Diseases 0.000 claims description 2
- 201000002481 Myositis Diseases 0.000 claims description 2
- 206010061302 Myringitis Diseases 0.000 claims description 2
- NWIBSHFKIJFRCO-WUDYKRTCSA-N Mytomycin Chemical compound C1N2C(C(C(C)=C(N)C3=O)=O)=C3[C@@H](COC(N)=O)[C@@]2(OC)[C@@H]2[C@H]1N2 NWIBSHFKIJFRCO-WUDYKRTCSA-N 0.000 claims description 2
- BLXXJMDCKKHMKV-UHFFFAOYSA-N Nabumetone Chemical compound C1=C(CCC(C)=O)C=CC2=CC(OC)=CC=C21 BLXXJMDCKKHMKV-UHFFFAOYSA-N 0.000 claims description 2
- DDUHZTYCFQRHIY-UHFFFAOYSA-N Negwer: 6874 Natural products COC1=CC(=O)CC(C)C11C(=O)C(C(OC)=CC(OC)=C2Cl)=C2O1 DDUHZTYCFQRHIY-UHFFFAOYSA-N 0.000 claims description 2
- 229930193140 Neomycin Natural products 0.000 claims description 2
- ZBBHBTPTTSWHBA-UHFFFAOYSA-N Nicardipine Chemical compound COC(=O)C1=C(C)NC(C)=C(C(=O)OCCN(C)CC=2C=CC=CC=2)C1C1=CC=CC([N+]([O-])=O)=C1 ZBBHBTPTTSWHBA-UHFFFAOYSA-N 0.000 claims description 2
- PHVGLTMQBUFIQQ-UHFFFAOYSA-N Nortryptiline Chemical compound C1CC2=CC=CC=C2C(=CCCNC)C2=CC=CC=C21 PHVGLTMQBUFIQQ-UHFFFAOYSA-N 0.000 claims description 2
- 206010030043 Ocular hypertension Diseases 0.000 claims description 2
- 208000010191 Osteitis Deformans Diseases 0.000 claims description 2
- 206010031264 Osteonecrosis Diseases 0.000 claims description 2
- 208000005141 Otitis Diseases 0.000 claims description 2
- 206010033078 Otitis media Diseases 0.000 claims description 2
- 208000027868 Paget disease Diseases 0.000 claims description 2
- 206010033645 Pancreatitis Diseases 0.000 claims description 2
- 208000018737 Parkinson disease Diseases 0.000 claims description 2
- AHOUBRCZNHFOSL-UHFFFAOYSA-N Paroxetine hydrochloride Natural products C1=CC(F)=CC=C1C1C(COC=2C=C3OCOC3=CC=2)CNCC1 AHOUBRCZNHFOSL-UHFFFAOYSA-N 0.000 claims description 2
- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Natural products N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 claims description 2
- 229930195708 Penicillin V Natural products 0.000 claims description 2
- 208000008469 Peptic Ulcer Diseases 0.000 claims description 2
- 208000031845 Pernicious anaemia Diseases 0.000 claims description 2
- RGCVKNLCSQQDEP-UHFFFAOYSA-N Perphenazine Chemical compound C1CN(CCO)CCN1CCCN1C2=CC(Cl)=CC=C2SC2=CC=CC=C21 RGCVKNLCSQQDEP-UHFFFAOYSA-N 0.000 claims description 2
- 206010067781 Pharyngeal abscess Diseases 0.000 claims description 2
- 201000007100 Pharyngitis Diseases 0.000 claims description 2
- QZVCTJOXCFMACW-UHFFFAOYSA-N Phenoxybenzamine Chemical compound C=1C=CC=CC=1CN(CCCl)C(C)COC1=CC=CC=C1 QZVCTJOXCFMACW-UHFFFAOYSA-N 0.000 claims description 2
- CXOFVDLJLONNDW-UHFFFAOYSA-N Phenytoin Chemical compound N1C(=O)NC(=O)C1(C=1C=CC=CC=1)C1=CC=CC=C1 CXOFVDLJLONNDW-UHFFFAOYSA-N 0.000 claims description 2
- JPYHHZQJCSQRJY-UHFFFAOYSA-N Phloroglucinol Natural products CCC=CCC=CCC=CCC=CCCCCC(=O)C1=C(O)C=C(O)C=C1O JPYHHZQJCSQRJY-UHFFFAOYSA-N 0.000 claims description 2
- GMZVRMREEHBGGF-UHFFFAOYSA-N Piracetam Chemical compound NC(=O)CN1CCCC1=O GMZVRMREEHBGGF-UHFFFAOYSA-N 0.000 claims description 2
- 206010035664 Pneumonia Diseases 0.000 claims description 2
- 208000007048 Polymyalgia Rheumatica Diseases 0.000 claims description 2
- 208000037062 Polyps Diseases 0.000 claims description 2
- 241000097929 Porphyria Species 0.000 claims description 2
- 208000010642 Porphyrias Diseases 0.000 claims description 2
- UCGJZJXOPSNTGZ-UHFFFAOYSA-M Prifinium bromide Chemical compound [Br-].CC1[N+](CC)(CC)CCC1=C(C=1C=CC=CC=1)C1=CC=CC=C1 UCGJZJXOPSNTGZ-UHFFFAOYSA-M 0.000 claims description 2
- 206010036774 Proctitis Diseases 0.000 claims description 2
- ZGUGWUXLJSTTMA-UHFFFAOYSA-N Promazinum Chemical compound C1=CC=C2N(CCCN(C)C)C3=CC=CC=C3SC2=C1 ZGUGWUXLJSTTMA-UHFFFAOYSA-N 0.000 claims description 2
- VVWYOYDLCMFIEM-UHFFFAOYSA-N Propantheline Chemical compound C1=CC=C2C(C(=O)OCC[N+](C)(C(C)C)C(C)C)C3=CC=CC=C3OC2=C1 VVWYOYDLCMFIEM-UHFFFAOYSA-N 0.000 claims description 2
- 201000004681 Psoriasis Diseases 0.000 claims description 2
- 201000001263 Psoriatic Arthritis Diseases 0.000 claims description 2
- 208000036824 Psoriatic arthropathy Diseases 0.000 claims description 2
- IKMPWMZBZSAONZ-UHFFFAOYSA-N Quazepam Chemical compound FC1=CC=CC=C1C1=NCC(=S)N(CC(F)(F)F)C2=CC=C(Cl)C=C12 IKMPWMZBZSAONZ-UHFFFAOYSA-N 0.000 claims description 2
- 208000013616 Respiratory Distress Syndrome Diseases 0.000 claims description 2
- 206010038910 Retinitis Diseases 0.000 claims description 2
- 208000003801 Retropharyngeal Abscess Diseases 0.000 claims description 2
- FTALBRSUTCGOEG-UHFFFAOYSA-N Riluzole Chemical compound C1=C(OC(F)(F)F)C=C2SC(N)=NC2=C1 FTALBRSUTCGOEG-UHFFFAOYSA-N 0.000 claims description 2
- RYMZZMVNJRMUDD-UHFFFAOYSA-N SJ000286063 Natural products C12C(OC(=O)C(C)(C)CC)CC(C)C=C2C=CC(C)C1CCC1CC(O)CC(=O)O1 RYMZZMVNJRMUDD-UHFFFAOYSA-N 0.000 claims description 2
- 241000447727 Scabies Species 0.000 claims description 2
- 206010040628 Sialoadenitis Diseases 0.000 claims description 2
- 208000006045 Spondylarthropathies Diseases 0.000 claims description 2
- XNKLLVCARDGLGL-JGVFFNPUSA-N Stavudine Chemical compound O=C1NC(=O)C(C)=CN1[C@H]1C=C[C@@H](CO)O1 XNKLLVCARDGLGL-JGVFFNPUSA-N 0.000 claims description 2
- 208000006011 Stroke Diseases 0.000 claims description 2
- QJJXYPPXXYFBGM-LFZNUXCKSA-N Tacrolimus Chemical compound C1C[C@@H](O)[C@H](OC)C[C@@H]1\C=C(/C)[C@@H]1[C@H](C)[C@@H](O)CC(=O)[C@H](CC=C)/C=C(C)/C[C@H](C)C[C@H](OC)[C@H]([C@H](C[C@H]2C)OC)O[C@@]2(O)C(=O)C(=O)N2CCCC[C@H]2C(=O)O1 QJJXYPPXXYFBGM-LFZNUXCKSA-N 0.000 claims description 2
- 108010053950 Teicoplanin Proteins 0.000 claims description 2
- 208000000491 Tendinopathy Diseases 0.000 claims description 2
- 206010043255 Tendonitis Diseases 0.000 claims description 2
- 239000004098 Tetracycline Substances 0.000 claims description 2
- WKDDRNSBRWANNC-UHFFFAOYSA-N Thienamycin Natural products C1C(SCCN)=C(C(O)=O)N2C(=O)C(C(O)C)C21 WKDDRNSBRWANNC-UHFFFAOYSA-N 0.000 claims description 2
- 208000026317 Tietze syndrome Diseases 0.000 claims description 2
- QTSXMEPZSHLZFF-UHFFFAOYSA-M Timepidium bromide Chemical compound [Br-].C1[N+](C)(C)CC(OC)CC1=C(C=1SC=CC=1)C1=CC=CS1 QTSXMEPZSHLZFF-UHFFFAOYSA-M 0.000 claims description 2
- 241000130764 Tinea Species 0.000 claims description 2
- SUJUHGSWHZTSEU-UHFFFAOYSA-N Tipranavir Natural products C1C(O)=C(C(CC)C=2C=C(NS(=O)(=O)C=3N=CC(=CC=3)C(F)(F)F)C=CC=2)C(=O)OC1(CCC)CCC1=CC=CC=C1 SUJUHGSWHZTSEU-UHFFFAOYSA-N 0.000 claims description 2
- IVTVGDXNLFLDRM-HNNXBMFYSA-N Tomudex Chemical compound C=1C=C2NC(C)=NC(=O)C2=CC=1CN(C)C1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)S1 IVTVGDXNLFLDRM-HNNXBMFYSA-N 0.000 claims description 2
- KJADKKWYZYXHBB-XBWDGYHZSA-N Topiramic acid Chemical compound C1O[C@@]2(COS(N)(=O)=O)OC(C)(C)O[C@H]2[C@@H]2OC(C)(C)O[C@@H]21 KJADKKWYZYXHBB-XBWDGYHZSA-N 0.000 claims description 2
- NGBFQHCMQULJNZ-UHFFFAOYSA-N Torsemide Chemical compound CC(C)NC(=O)NS(=O)(=O)C1=CN=CC=C1NC1=CC=CC(C)=C1 NGBFQHCMQULJNZ-UHFFFAOYSA-N 0.000 claims description 2
- YPTFHLJNWSJXKG-UHFFFAOYSA-N Trepibutone Chemical compound CCOC1=CC(OCC)=C(C(=O)CCC(O)=O)C=C1OCC YPTFHLJNWSJXKG-UHFFFAOYSA-N 0.000 claims description 2
- FNYLWPVRPXGIIP-UHFFFAOYSA-N Triamterene Chemical compound NC1=NC2=NC(N)=NC(N)=C2N=C1C1=CC=CC=C1 FNYLWPVRPXGIIP-UHFFFAOYSA-N 0.000 claims description 2
- 241000893966 Trichophyton verrucosum Species 0.000 claims description 2
- 206010067584 Type 1 diabetes mellitus Diseases 0.000 claims description 2
- HDOVUKNUBWVHOX-QMMMGPOBSA-N Valacyclovir Chemical compound N1C(N)=NC(=O)C2=C1N(COCCOC(=O)[C@@H](N)C(C)C)C=N2 HDOVUKNUBWVHOX-QMMMGPOBSA-N 0.000 claims description 2
- 108010059993 Vancomycin Proteins 0.000 claims description 2
- 208000036142 Viral infection Diseases 0.000 claims description 2
- 206010047700 Vomiting Diseases 0.000 claims description 2
- 208000027207 Whipple disease Diseases 0.000 claims description 2
- QRUAPADZILXULG-WKIKZPBSSA-N Zuclopenthixol decanoate Chemical compound C1CN(CCOC(=O)CCCCCCCCC)CCN1CC\C=C\1C2=CC(Cl)=CC=C2SC2=CC=CC=C2/1 QRUAPADZILXULG-WKIKZPBSSA-N 0.000 claims description 2
- WPUKUEMZZRVAKZ-NFBKMPQASA-N [(1r,3r)-1-ethyl-1-methylpiperidin-1-ium-3-yl] 2-hydroxy-2,2-diphenylacetate Chemical compound C1[N@@+](CC)(C)CCC[C@H]1OC(=O)C(O)(C=1C=CC=CC=1)C1=CC=CC=C1 WPUKUEMZZRVAKZ-NFBKMPQASA-N 0.000 claims description 2
- WNPNNLQNNJQYFA-UHFFFAOYSA-N [2-(3,4-dihydroxyphenyl)-2-hydroxyethyl]azanium;2,3,4-trihydroxy-4-oxobutanoate Chemical compound OC(=O)C(O)C(O)C(O)=O.NCC(O)C1=CC=C(O)C(O)=C1 WNPNNLQNNJQYFA-UHFFFAOYSA-N 0.000 claims description 2
- 229960004748 abacavir Drugs 0.000 claims description 2
- MCGSCOLBFJQGHM-SCZZXKLOSA-N abacavir Chemical compound C=12N=CN([C@H]3C=C[C@@H](CO)C3)C2=NC(N)=NC=1NC1CC1 MCGSCOLBFJQGHM-SCZZXKLOSA-N 0.000 claims description 2
- 229960000446 abciximab Drugs 0.000 claims description 2
- 229960004150 aciclovir Drugs 0.000 claims description 2
- MKUXAQIIEYXACX-UHFFFAOYSA-N aciclovir Chemical compound N1C(N)=NC(=O)C2=C1N(COCCO)C=N2 MKUXAQIIEYXACX-UHFFFAOYSA-N 0.000 claims description 2
- 206010000496 acne Diseases 0.000 claims description 2
- RJURFGZVJUQBHK-IIXSONLDSA-N actinomycin D Chemical compound C[C@H]1OC(=O)[C@H](C(C)C)N(C)C(=O)CN(C)C(=O)[C@@H]2CCCN2C(=O)[C@@H](C(C)C)NC(=O)[C@H]1NC(=O)C1=C(N)C(=O)C(C)=C2OC(C(C)=CC=C3C(=O)N[C@@H]4C(=O)N[C@@H](C(N5CCC[C@H]5C(=O)N(C)CC(=O)N(C)[C@@H](C(C)C)C(=O)O[C@@H]4C)=O)C(C)C)=C3N=C21 RJURFGZVJUQBHK-IIXSONLDSA-N 0.000 claims description 2
- 208000002552 acute disseminated encephalomyelitis Diseases 0.000 claims description 2
- 230000001154 acute effect Effects 0.000 claims description 2
- 206010000891 acute myocardial infarction Diseases 0.000 claims description 2
- 208000005298 acute pain Diseases 0.000 claims description 2
- WOZSCQDILHKSGG-UHFFFAOYSA-N adefovir depivoxil Chemical compound N1=CN=C2N(CCOCP(=O)(OCOC(=O)C(C)(C)C)OCOC(=O)C(C)(C)C)C=NC2=C1N WOZSCQDILHKSGG-UHFFFAOYSA-N 0.000 claims description 2
- 229960005305 adenosine Drugs 0.000 claims description 2
- 201000000028 adult respiratory distress syndrome Diseases 0.000 claims description 2
- 229960002629 agomelatine Drugs 0.000 claims description 2
- YJYPHIXNFHFHND-UHFFFAOYSA-N agomelatine Chemical compound C1=CC=C(CCNC(C)=O)C2=CC(OC)=CC=C21 YJYPHIXNFHFHND-UHFFFAOYSA-N 0.000 claims description 2
- 229940083712 aldosterone antagonist Drugs 0.000 claims description 2
- 239000002170 aldosterone antagonist Substances 0.000 claims description 2
- 235000010443 alginic acid Nutrition 0.000 claims description 2
- 229920000615 alginic acid Polymers 0.000 claims description 2
- 229960004601 aliskiren Drugs 0.000 claims description 2
- 208000026935 allergic disease Diseases 0.000 claims description 2
- 230000007815 allergy Effects 0.000 claims description 2
- 231100000360 alopecia Toxicity 0.000 claims description 2
- RYHCACJBKCOBTJ-UHFFFAOYSA-N alverine citrate Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O.C=1C=CC=CC=1CCCN(CC)CCCC1=CC=CC=C1 RYHCACJBKCOBTJ-UHFFFAOYSA-N 0.000 claims description 2
- 229960001306 alverine citrate Drugs 0.000 claims description 2
- 229960002414 ambrisentan Drugs 0.000 claims description 2
- 229960004821 amikacin Drugs 0.000 claims description 2
- LKCWBDHBTVXHDL-RMDFUYIESA-N amikacin Chemical compound O([C@@H]1[C@@H](N)C[C@H]([C@@H]([C@H]1O)O[C@@H]1[C@@H]([C@@H](N)[C@H](O)[C@@H](CO)O1)O)NC(=O)[C@@H](O)CCN)[C@H]1O[C@H](CN)[C@@H](O)[C@H](O)[C@H]1O LKCWBDHBTVXHDL-RMDFUYIESA-N 0.000 claims description 2
- 229960004104 amiloride hydrochloride Drugs 0.000 claims description 2
- 229960003234 amiodarone hydrochloride Drugs 0.000 claims description 2
- 229960000528 amlodipine Drugs 0.000 claims description 2
- HTIQEAQVCYTUBX-UHFFFAOYSA-N amlodipine Chemical compound CCOC(=O)C1=C(COCCN)NC(C)=C(C(=O)OC)C1C1=CC=CC=C1Cl HTIQEAQVCYTUBX-UHFFFAOYSA-N 0.000 claims description 2
- 229960003022 amoxicillin Drugs 0.000 claims description 2
- LSQZJLSUYDQPKJ-NJBDSQKTSA-N amoxicillin Chemical compound C1([C@@H](N)C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C(O)=O)(C)C)=CC=C(O)C=C1 LSQZJLSUYDQPKJ-NJBDSQKTSA-N 0.000 claims description 2
- 229940009444 amphotericin Drugs 0.000 claims description 2
- APKFDSVGJQXUKY-INPOYWNPSA-N amphotericin B Chemical compound O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/C=C/C=C/C=C/[C@H](C)[C@@H](O)[C@@H](C)[C@H](C)OC(=O)C[C@H](O)C[C@H](O)CC[C@@H](O)[C@H](O)C[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 APKFDSVGJQXUKY-INPOYWNPSA-N 0.000 claims description 2
- 229960000723 ampicillin Drugs 0.000 claims description 2
- AVKUERGKIZMTKX-NJBDSQKTSA-N ampicillin Chemical compound C1([C@@H](N)C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C(O)=O)(C)C)=CC=CC=C1 AVKUERGKIZMTKX-NJBDSQKTSA-N 0.000 claims description 2
- 229960003348 anidulafungin Drugs 0.000 claims description 2
- JHVAMHSQVVQIOT-MFAJLEFUSA-N anidulafungin Chemical compound C1=CC(OCCCCC)=CC=C1C1=CC=C(C=2C=CC(=CC=2)C(=O)N[C@@H]2C(N[C@H](C(=O)N3C[C@H](O)C[C@H]3C(=O)N[C@H](C(=O)N[C@H](C(=O)N3C[C@H](C)[C@H](O)[C@H]3C(=O)N[C@H](O)[C@H](O)C2)[C@@H](C)O)[C@H](O)[C@@H](O)C=2C=CC(O)=CC=2)[C@@H](C)O)=O)C=C1 JHVAMHSQVVQIOT-MFAJLEFUSA-N 0.000 claims description 2
- 229940069428 antacid Drugs 0.000 claims description 2
- 239000003159 antacid agent Substances 0.000 claims description 2
- 230000001567 anti-fibrinolytic effect Effects 0.000 claims description 2
- 230000002921 anti-spasmodic effect Effects 0.000 claims description 2
- 239000003146 anticoagulant agent Substances 0.000 claims description 2
- 229940127219 anticoagulant drug Drugs 0.000 claims description 2
- 229940127218 antiplatelet drug Drugs 0.000 claims description 2
- 229940124575 antispasmodic agent Drugs 0.000 claims description 2
- 229960004046 apomorphine Drugs 0.000 claims description 2
- VMWNQDUVQKEIOC-CYBMUJFWSA-N apomorphine Chemical compound C([C@H]1N(C)CC2)C3=CC=C(O)C(O)=C3C3=C1C2=CC=C3 VMWNQDUVQKEIOC-CYBMUJFWSA-N 0.000 claims description 2
- 230000006793 arrhythmia Effects 0.000 claims description 2
- 206010003119 arrhythmia Diseases 0.000 claims description 2
- 208000021328 arterial occlusion Diseases 0.000 claims description 2
- 206010003246 arthritis Diseases 0.000 claims description 2
- 208000006673 asthma Diseases 0.000 claims description 2
- 208000010668 atopic eczema Diseases 0.000 claims description 2
- 229960005370 atorvastatin Drugs 0.000 claims description 2
- 229960003159 atovaquone Drugs 0.000 claims description 2
- KUCQYCKVKVOKAY-CTYIDZIISA-N atovaquone Chemical compound C1([C@H]2CC[C@@H](CC2)C2=C(C(C3=CC=CC=C3C2=O)=O)O)=CC=C(Cl)C=C1 KUCQYCKVKVOKAY-CTYIDZIISA-N 0.000 claims description 2
- 229960002028 atropine sulfate Drugs 0.000 claims description 2
- 230000001363 autoimmune Effects 0.000 claims description 2
- 229960002756 azacitidine Drugs 0.000 claims description 2
- 229960004099 azithromycin Drugs 0.000 claims description 2
- MQTOSJVFKKJCRP-BICOPXKESA-N azithromycin Chemical compound O([C@@H]1[C@@H](C)C(=O)O[C@@H]([C@@]([C@H](O)[C@@H](C)N(C)C[C@H](C)C[C@@](C)(O)[C@H](O[C@H]2[C@@H]([C@H](C[C@@H](C)O2)N(C)C)O)[C@H]1C)(C)O)CC)[C@H]1C[C@@](C)(OC)[C@@H](O)[C@H](C)O1 MQTOSJVFKKJCRP-BICOPXKESA-N 0.000 claims description 2
- 229960003644 aztreonam Drugs 0.000 claims description 2
- WZPBZJONDBGPKJ-VEHQQRBSSA-N aztreonam Chemical compound O=C1N(S([O-])(=O)=O)[C@@H](C)[C@@H]1NC(=O)C(=N/OC(C)(C)C(O)=O)\C1=CSC([NH3+])=N1 WZPBZJONDBGPKJ-VEHQQRBSSA-N 0.000 claims description 2
- 229940092705 beclomethasone Drugs 0.000 claims description 2
- 229960003515 bendroflumethiazide Drugs 0.000 claims description 2
- 229960002507 benperidol Drugs 0.000 claims description 2
- 229960002537 betamethasone Drugs 0.000 claims description 2
- UREBDLICKHMUKA-DVTGEIKXSA-N betamethasone Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@H](C)[C@@](C(=O)CO)(O)[C@@]1(C)C[C@@H]2O UREBDLICKHMUKA-DVTGEIKXSA-N 0.000 claims description 2
- 229960003307 bevonium Drugs 0.000 claims description 2
- UHUMRJKDOOEQIG-UHFFFAOYSA-N bevonium Chemical compound C[N+]1(C)CCCCC1COC(=O)C(O)(C=1C=CC=CC=1)C1=CC=CC=C1 UHUMRJKDOOEQIG-UHFFFAOYSA-N 0.000 claims description 2
- 229960000516 bezafibrate Drugs 0.000 claims description 2
- IIBYAHWJQTYFKB-UHFFFAOYSA-N bezafibrate Chemical compound C1=CC(OC(C)(C)C(O)=O)=CC=C1CCNC(=O)C1=CC=C(Cl)C=C1 IIBYAHWJQTYFKB-UHFFFAOYSA-N 0.000 claims description 2
- 229920000080 bile acid sequestrant Polymers 0.000 claims description 2
- 229940096699 bile acid sequestrants Drugs 0.000 claims description 2
- 108010055460 bivalirudin Proteins 0.000 claims description 2
- 229960001500 bivalirudin Drugs 0.000 claims description 2
- OIRCOABEOLEUMC-GEJPAHFPSA-N bivalirudin Chemical compound C([C@@H](C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(=O)N[C@@H](CC(C)C)C(O)=O)NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CC(N)=O)NC(=O)CNC(=O)CNC(=O)CNC(=O)CNC(=O)[C@H]1N(CCC1)C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H]1N(CCC1)C(=O)[C@H](N)CC=1C=CC=CC=1)C1=CC=CC=C1 OIRCOABEOLEUMC-GEJPAHFPSA-N 0.000 claims description 2
- 229960001561 bleomycin Drugs 0.000 claims description 2
- OYVAGSVQBOHSSS-UAPAGMARSA-O bleomycin A2 Chemical compound N([C@H](C(=O)N[C@H](C)[C@@H](O)[C@H](C)C(=O)N[C@@H]([C@H](O)C)C(=O)NCCC=1SC=C(N=1)C=1SC=C(N=1)C(=O)NCCC[S+](C)C)[C@@H](O[C@H]1[C@H]([C@@H](O)[C@H](O)[C@H](CO)O1)O[C@@H]1[C@H]([C@@H](OC(N)=O)[C@H](O)[C@@H](CO)O1)O)C=1N=CNC=1)C(=O)C1=NC([C@H](CC(N)=O)NC[C@H](N)C(N)=O)=NC(N)=C1C OYVAGSVQBOHSSS-UAPAGMARSA-O 0.000 claims description 2
- 208000010217 blepharitis Diseases 0.000 claims description 2
- 230000000903 blocking effect Effects 0.000 claims description 2
- 229960003065 bosentan Drugs 0.000 claims description 2
- GJPICJJJRGTNOD-UHFFFAOYSA-N bosentan Chemical compound COC1=CC=CC=C1OC(C(=NC(=N1)C=2N=CC=CN=2)OCCO)=C1NS(=O)(=O)C1=CC=C(C(C)(C)C)C=C1 GJPICJJJRGTNOD-UHFFFAOYSA-N 0.000 claims description 2
- 206010006475 bronchopulmonary dysplasia Diseases 0.000 claims description 2
- 229960004064 bumetanide Drugs 0.000 claims description 2
- MAEIEVLCKWDQJH-UHFFFAOYSA-N bumetanide Chemical compound CCCCNC1=CC(C(O)=O)=CC(S(N)(=O)=O)=C1OC1=CC=CC=C1 MAEIEVLCKWDQJH-UHFFFAOYSA-N 0.000 claims description 2
- IFKLAQQSCNILHL-QHAWAJNXSA-N butorphanol Chemical compound N1([C@@H]2CC3=CC=C(C=C3[C@@]3([C@]2(CCCC3)O)CC1)O)CC1CCC1 IFKLAQQSCNILHL-QHAWAJNXSA-N 0.000 claims description 2
- 239000000480 calcium channel blocker Substances 0.000 claims description 2
- 229960004117 capecitabine Drugs 0.000 claims description 2
- 229960004602 capreomycin Drugs 0.000 claims description 2
- FFGPTBGBLSHEPO-UHFFFAOYSA-N carbamazepine Chemical compound C1=CC2=CC=CC=C2N(C(=O)N)C2=CC=CC=C21 FFGPTBGBLSHEPO-UHFFFAOYSA-N 0.000 claims description 2
- 229960000623 carbamazepine Drugs 0.000 claims description 2
- 229940097217 cardiac glycoside Drugs 0.000 claims description 2
- 239000002368 cardiac glycoside Substances 0.000 claims description 2
- 229940082638 cardiac stimulant phosphodiesterase inhibitors Drugs 0.000 claims description 2
- MSPRUJDUTKRMLM-UHFFFAOYSA-N caroverine Chemical compound O=C1N(CCN(CC)CC)C2=CC=CC=C2N=C1CC1=CC=C(OC)C=C1 MSPRUJDUTKRMLM-UHFFFAOYSA-N 0.000 claims description 2
- 229960003034 caspofungin Drugs 0.000 claims description 2
- JYIKNQVWKBUSNH-WVDDFWQHSA-N caspofungin Chemical compound C1([C@H](O)[C@@H](O)[C@H]2C(=O)N[C@H](C(=O)N3CC[C@H](O)[C@H]3C(=O)N[C@H](NCCN)[C@H](O)C[C@@H](C(N[C@H](C(=O)N3C[C@H](O)C[C@H]3C(=O)N2)[C@@H](C)O)=O)NC(=O)CCCCCCCC[C@@H](C)C[C@@H](C)CC)[C@H](O)CCN)=CC=C(O)C=C1 JYIKNQVWKBUSNH-WVDDFWQHSA-N 0.000 claims description 2
- 239000004359 castor oil Substances 0.000 claims description 2
- 235000019438 castor oil Nutrition 0.000 claims description 2
- 229960005361 cefaclor Drugs 0.000 claims description 2
- QYIYFLOTGYLRGG-GPCCPHFNSA-N cefaclor Chemical compound C1([C@H](C(=O)N[C@@H]2C(N3C(=C(Cl)CS[C@@H]32)C(O)=O)=O)N)=CC=CC=C1 QYIYFLOTGYLRGG-GPCCPHFNSA-N 0.000 claims description 2
- 210000003169 central nervous system Anatomy 0.000 claims description 2
- 208000015114 central nervous system disease Diseases 0.000 claims description 2
- 229940124587 cephalosporin Drugs 0.000 claims description 2
- 150000001780 cephalosporins Chemical class 0.000 claims description 2
- DDTDNCYHLGRFBM-YZEKDTGTSA-N chembl2367892 Chemical compound CC(=O)N[C@H]1[C@@H](O)[C@H](O)[C@H](CO)O[C@H]1O[C@@H]([C@H]1C(N[C@@H](C2=CC(O)=CC(O[C@@H]3[C@H]([C@H](O)[C@H](O)[C@@H](CO)O3)O)=C2C=2C(O)=CC=C(C=2)[C@@H](NC(=O)[C@@H]2NC(=O)[C@@H]3C=4C=C(O)C=C(C=4)OC=4C(O)=CC=C(C=4)[C@@H](N)C(=O)N[C@H](CC=4C=C(Cl)C(O5)=CC=4)C(=O)N3)C(=O)N1)C(O)=O)=O)C(C=C1Cl)=CC=C1OC1=C(O[C@H]3[C@H]([C@@H](O)[C@H](O)[C@H](CO)O3)NC(C)=O)C5=CC2=C1 DDTDNCYHLGRFBM-YZEKDTGTSA-N 0.000 claims description 2
- 229960005091 chloramphenicol Drugs 0.000 claims description 2
- WIIZWVCIJKGZOK-RKDXNWHRSA-N chloramphenicol Chemical compound ClC(Cl)C(=O)N[C@H](CO)[C@H](O)C1=CC=C([N+]([O-])=O)C=C1 WIIZWVCIJKGZOK-RKDXNWHRSA-N 0.000 claims description 2
- 229960003078 chlorbenzoxamine Drugs 0.000 claims description 2
- VEVSKUJZSMGTMM-UHFFFAOYSA-N chlorbenzoxamine Chemical compound CC1=CC=CC=C1CN1CCN(CCOC(C=2C=CC=CC=2)C=2C(=CC=CC=2)Cl)CC1 VEVSKUJZSMGTMM-UHFFFAOYSA-N 0.000 claims description 2
- 229960003677 chloroquine Drugs 0.000 claims description 2
- WHTVZRBIWZFKQO-UHFFFAOYSA-N chloroquine Natural products ClC1=CC=C2C(NC(C)CCCN(CC)CC)=CC=NC2=C1 WHTVZRBIWZFKQO-UHFFFAOYSA-N 0.000 claims description 2
- 229960001076 chlorpromazine Drugs 0.000 claims description 2
- ZPEIMTDSQAKGNT-UHFFFAOYSA-N chlorpromazine Chemical compound C1=C(Cl)C=C2N(CCCN(C)C)C3=CC=CC=C3SC2=C1 ZPEIMTDSQAKGNT-UHFFFAOYSA-N 0.000 claims description 2
- 208000019069 chronic childhood arthritis Diseases 0.000 claims description 2
- 208000014797 chronic intestinal pseudoobstruction Diseases 0.000 claims description 2
- 229960000724 cidofovir Drugs 0.000 claims description 2
- 229960005025 cilazapril Drugs 0.000 claims description 2
- HHHKFGXWKKUNCY-FHWLQOOXSA-N cilazapril Chemical compound C([C@@H](C(=O)OCC)N[C@@H]1C(N2[C@@H](CCCN2CCC1)C(O)=O)=O)CC1=CC=CC=C1 HHHKFGXWKKUNCY-FHWLQOOXSA-N 0.000 claims description 2
- 229960004588 cilostazol Drugs 0.000 claims description 2
- LOUPRKONTZGTKE-UHFFFAOYSA-N cinchonine Natural products C1C(C(C2)C=C)CCN2C1C(O)C1=CC=NC2=CC=C(OC)C=C21 LOUPRKONTZGTKE-UHFFFAOYSA-N 0.000 claims description 2
- 229960002174 ciprofibrate Drugs 0.000 claims description 2
- KPSRODZRAIWAKH-UHFFFAOYSA-N ciprofibrate Chemical compound C1=CC(OC(C)(C)C(O)=O)=CC=C1C1C(Cl)(Cl)C1 KPSRODZRAIWAKH-UHFFFAOYSA-N 0.000 claims description 2
- 230000007882 cirrhosis Effects 0.000 claims description 2
- 208000019425 cirrhosis of liver Diseases 0.000 claims description 2
- 229960001653 citalopram Drugs 0.000 claims description 2
- 229960002436 cladribine Drugs 0.000 claims description 2
- 229960002626 clarithromycin Drugs 0.000 claims description 2
- AGOYDEPGAOXOCK-KCBOHYOISA-N clarithromycin Chemical compound O([C@@H]1[C@@H](C)C(=O)O[C@@H]([C@@]([C@H](O)[C@@H](C)C(=O)[C@H](C)C[C@](C)([C@H](O[C@H]2[C@@H]([C@H](C[C@@H](C)O2)N(C)C)O)[C@H]1C)OC)(C)O)CC)[C@H]1C[C@@](C)(OC)[C@@H](O)[C@H](C)O1 AGOYDEPGAOXOCK-KCBOHYOISA-N 0.000 claims description 2
- 229960002227 clindamycin Drugs 0.000 claims description 2
- KDLRVYVGXIQJDK-AWPVFWJPSA-N clindamycin Chemical compound CN1C[C@H](CCC)C[C@H]1C(=O)N[C@H]([C@H](C)Cl)[C@@H]1[C@H](O)[C@H](O)[C@@H](O)[C@@H](SC)O1 KDLRVYVGXIQJDK-AWPVFWJPSA-N 0.000 claims description 2
- 229960000928 clofarabine Drugs 0.000 claims description 2
- WDDPHFBMKLOVOX-AYQXTPAHSA-N clofarabine Chemical compound C1=NC=2C(N)=NC(Cl)=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@@H]1F WDDPHFBMKLOVOX-AYQXTPAHSA-N 0.000 claims description 2
- 229960004287 clofazimine Drugs 0.000 claims description 2
- WDQPAMHFFCXSNU-BGABXYSRSA-N clofazimine Chemical compound C12=CC=CC=C2N=C2C=C(NC=3C=CC(Cl)=CC=3)C(=N/C(C)C)/C=C2N1C1=CC=C(Cl)C=C1 WDQPAMHFFCXSNU-BGABXYSRSA-N 0.000 claims description 2
- 229960004414 clomethiazole Drugs 0.000 claims description 2
- 229960002896 clonidine Drugs 0.000 claims description 2
- 229940047766 co-trimoxazole Drugs 0.000 claims description 2
- 229960002604 colestipol Drugs 0.000 claims description 2
- GMRWGQCZJGVHKL-UHFFFAOYSA-N colestipol Chemical compound ClCC1CO1.NCCNCCNCCNCCN GMRWGQCZJGVHKL-UHFFFAOYSA-N 0.000 claims description 2
- 229960003346 colistin Drugs 0.000 claims description 2
- 230000000112 colonic effect Effects 0.000 claims description 2
- 239000003246 corticosteroid Substances 0.000 claims description 2
- 229960001334 corticosteroids Drugs 0.000 claims description 2
- 229960004544 cortisone Drugs 0.000 claims description 2
- 229960000684 cytarabine Drugs 0.000 claims description 2
- KWGRBVOPPLSCSI-UHFFFAOYSA-N d-ephedrine Natural products CNC(C)C(O)C1=CC=CC=C1 KWGRBVOPPLSCSI-UHFFFAOYSA-N 0.000 claims description 2
- 229960003850 dabigatran Drugs 0.000 claims description 2
- YBSJFWOBGCMAKL-UHFFFAOYSA-N dabigatran Chemical compound N=1C2=CC(C(=O)N(CCC(O)=O)C=3N=CC=CC=3)=CC=C2N(C)C=1CNC1=CC=C(C(N)=N)C=C1 YBSJFWOBGCMAKL-UHFFFAOYSA-N 0.000 claims description 2
- 229960000640 dactinomycin Drugs 0.000 claims description 2
- 229960003828 danaparoid Drugs 0.000 claims description 2
- 229960000860 dapsone Drugs 0.000 claims description 2
- 229960005484 daptomycin Drugs 0.000 claims description 2
- DOAKLVKFURWEDJ-QCMAZARJSA-N daptomycin Chemical compound C([C@H]1C(=O)O[C@H](C)[C@@H](C(NCC(=O)N[C@@H](CCCN)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@H](C)C(=O)N[C@@H](CC(O)=O)C(=O)NCC(=O)N[C@H](CO)C(=O)N[C@H](C(=O)N1)[C@H](C)CC(O)=O)=O)NC(=O)[C@H](CC(O)=O)NC(=O)[C@@H](CC(N)=O)NC(=O)[C@H](CC=1C2=CC=CC=C2NC=1)NC(=O)CCCCCCCCC)C(=O)C1=CC=CC=C1N DOAKLVKFURWEDJ-QCMAZARJSA-N 0.000 claims description 2
- STQGQHZAVUOBTE-VGBVRHCVSA-N daunorubicin Chemical compound O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(C)=O)[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 STQGQHZAVUOBTE-VGBVRHCVSA-N 0.000 claims description 2
- 229960000975 daunorubicin Drugs 0.000 claims description 2
- 229960001145 deflazacort Drugs 0.000 claims description 2
- FBHSPRKOSMHSIF-GRMWVWQJSA-N deflazacort Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@@H]2[C@@H]1[C@@H]1C[C@H]3OC(C)=N[C@@]3(C(=O)COC(=O)C)[C@@]1(C)C[C@@H]2O FBHSPRKOSMHSIF-GRMWVWQJSA-N 0.000 claims description 2
- 229960002398 demeclocycline Drugs 0.000 claims description 2
- 230000001419 dependent effect Effects 0.000 claims description 2
- 229960003957 dexamethasone Drugs 0.000 claims description 2
- UREBDLICKHMUKA-CXSFZGCWSA-N dexamethasone Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@@H](C)[C@@](C(=O)CO)(O)[C@@]1(C)C[C@@H]2O UREBDLICKHMUKA-CXSFZGCWSA-N 0.000 claims description 2
- 208000033679 diabetic kidney disease Diseases 0.000 claims description 2
- GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 claims description 2
- 229960004042 diazoxide Drugs 0.000 claims description 2
- 229960002656 didanosine Drugs 0.000 claims description 2
- 229960000616 diflunisal Drugs 0.000 claims description 2
- HUPFGZXOMWLGNK-UHFFFAOYSA-N diflunisal Chemical compound C1=C(O)C(C(=O)O)=CC(C=2C(=CC(F)=CC=2)F)=C1 HUPFGZXOMWLGNK-UHFFFAOYSA-N 0.000 claims description 2
- 210000002249 digestive system Anatomy 0.000 claims description 2
- 229960000648 digitoxin Drugs 0.000 claims description 2
- WDJUZGPOPHTGOT-XUDUSOBPSA-N digitoxin Chemical compound C1[C@H](O)[C@H](O)[C@@H](C)O[C@H]1O[C@@H]1[C@@H](C)O[C@@H](O[C@@H]2[C@H](O[C@@H](O[C@@H]3C[C@@H]4[C@]([C@@H]5[C@H]([C@]6(CC[C@@H]([C@@]6(C)CC5)C=5COC(=O)C=5)O)CC4)(C)CC3)C[C@@H]2O)C)C[C@@H]1O WDJUZGPOPHTGOT-XUDUSOBPSA-N 0.000 claims description 2
- 229960005156 digoxin Drugs 0.000 claims description 2
- LTMHDMANZUZIPE-UHFFFAOYSA-N digoxine Natural products C1C(O)C(O)C(C)OC1OC1C(C)OC(OC2C(OC(OC3CC4C(C5C(C6(CCC(C6(C)C(O)C5)C=5COC(=O)C=5)O)CC4)(C)CC3)CC2O)C)CC1O LTMHDMANZUZIPE-UHFFFAOYSA-N 0.000 claims description 2
- 229960003215 dihexyverine Drugs 0.000 claims description 2
- MNSQDVCVWNXBFQ-UHFFFAOYSA-N dihexyverine Chemical compound C1CCCCC1(C1CCCCC1)C(=O)OCCN1CCCCC1 MNSQDVCVWNXBFQ-UHFFFAOYSA-N 0.000 claims description 2
- SXYIRMFQILZOAM-HVNFFKDJSA-N dihydroartemisinin methyl ether Chemical compound C1C[C@H]2[C@H](C)CC[C@H]3[C@@H](C)[C@@H](OC)O[C@H]4[C@]32OO[C@@]1(C)O4 SXYIRMFQILZOAM-HVNFFKDJSA-N 0.000 claims description 2
- 229960004071 diisopromine Drugs 0.000 claims description 2
- YBJKOPHEJOMRMN-UHFFFAOYSA-N diisopromine Chemical compound C=1C=CC=CC=1C(CCN(C(C)C)C(C)C)C1=CC=CC=C1 YBJKOPHEJOMRMN-UHFFFAOYSA-N 0.000 claims description 2
- 229960003497 diloxanide furoate Drugs 0.000 claims description 2
- BDYYDXJSHYEDGB-UHFFFAOYSA-N diloxanide furoate Chemical compound C1=CC(N(C(=O)C(Cl)Cl)C)=CC=C1OC(=O)C1=CC=CO1 BDYYDXJSHYEDGB-UHFFFAOYSA-N 0.000 claims description 2
- HSUGRBWQSSZJOP-RTWAWAEBSA-N diltiazem Chemical compound C1=CC(OC)=CC=C1[C@H]1[C@@H](OC(C)=O)C(=O)N(CCN(C)C)C2=CC=CC=C2S1 HSUGRBWQSSZJOP-RTWAWAEBSA-N 0.000 claims description 2
- 229960004166 diltiazem Drugs 0.000 claims description 2
- GXGAKHNRMVGRPK-UHFFFAOYSA-N dimagnesium;dioxido-bis[[oxido(oxo)silyl]oxy]silane Chemical compound [Mg+2].[Mg+2].[O-][Si](=O)O[Si]([O-])([O-])O[Si]([O-])=O GXGAKHNRMVGRPK-UHFFFAOYSA-N 0.000 claims description 2
- 229960005116 diphemanil Drugs 0.000 claims description 2
- ZZVUWRFHKOJYTH-UHFFFAOYSA-N diphenhydramine Chemical compound C=1C=CC=CC=1C(OCCN(C)C)C1=CC=CC=C1 ZZVUWRFHKOJYTH-UHFFFAOYSA-N 0.000 claims description 2
- 229960002768 dipyridamole Drugs 0.000 claims description 2
- IZEKFCXSFNUWAM-UHFFFAOYSA-N dipyridamole Chemical compound C=12N=C(N(CCO)CCO)N=C(N3CCCCC3)C2=NC(N(CCO)CCO)=NC=1N1CCCCC1 IZEKFCXSFNUWAM-UHFFFAOYSA-N 0.000 claims description 2
- UVTNFZQICZKOEM-UHFFFAOYSA-N disopyramide Chemical compound C=1C=CC=NC=1C(C(N)=O)(CCN(C(C)C)C(C)C)C1=CC=CC=C1 UVTNFZQICZKOEM-UHFFFAOYSA-N 0.000 claims description 2
- 229960001066 disopyramide Drugs 0.000 claims description 2
- 208000007784 diverticulitis Diseases 0.000 claims description 2
- 229960003530 donepezil Drugs 0.000 claims description 2
- 229960003638 dopamine Drugs 0.000 claims description 2
- 239000003210 dopamine receptor blocking agent Substances 0.000 claims description 2
- 229960001857 dopexamine Drugs 0.000 claims description 2
- RYBJORHCUPVNMB-UHFFFAOYSA-N dopexamine Chemical compound C1=C(O)C(O)=CC=C1CCNCCCCCCNCCC1=CC=CC=C1 RYBJORHCUPVNMB-UHFFFAOYSA-N 0.000 claims description 2
- 229960001393 dosulepin Drugs 0.000 claims description 2
- 229960002866 duloxetine Drugs 0.000 claims description 2
- 208000019258 ear infection Diseases 0.000 claims description 2
- XPOQHMRABVBWPR-ZDUSSCGKSA-N efavirenz Chemical compound C([C@]1(C2=CC(Cl)=CC=C2NC(=O)O1)C(F)(F)F)#CC1CC1 XPOQHMRABVBWPR-ZDUSSCGKSA-N 0.000 claims description 2
- 229960003804 efavirenz Drugs 0.000 claims description 2
- 229960000366 emtricitabine Drugs 0.000 claims description 2
- OYFJQPXVCSSHAI-QFPUQLAESA-N enalapril maleate Chemical compound OC(=O)\C=C/C(O)=O.C([C@@H](C(=O)OCC)N[C@@H](C)C(=O)N1[C@@H](CCC1)C(O)=O)CC1=CC=CC=C1 OYFJQPXVCSSHAI-QFPUQLAESA-N 0.000 claims description 2
- 229960000309 enalapril maleate Drugs 0.000 claims description 2
- 206010014599 encephalitis Diseases 0.000 claims description 2
- 206010014665 endocarditis Diseases 0.000 claims description 2
- 230000002124 endocrine Effects 0.000 claims description 2
- 229960000610 enoxaparin Drugs 0.000 claims description 2
- 229960000972 enoximone Drugs 0.000 claims description 2
- 229960002179 ephedrine Drugs 0.000 claims description 2
- 229960001123 epoprostenol Drugs 0.000 claims description 2
- 229960004468 eptifibatide Drugs 0.000 claims description 2
- GLGOPUHVAZCPRB-LROMGURASA-N eptifibatide Chemical compound N1C(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCCNC(=N)N)NC(=O)CCSSC[C@@H](C(N)=O)NC(=O)[C@@H]2CCCN2C(=O)[C@@H]1CC1=CN=C2[C]1C=CC=C2 GLGOPUHVAZCPRB-LROMGURASA-N 0.000 claims description 2
- 208000004000 erythrasma Diseases 0.000 claims description 2
- 229960003276 erythromycin Drugs 0.000 claims description 2
- 229960004341 escitalopram Drugs 0.000 claims description 2
- WSEQXVZVJXJVFP-FQEVSTJZSA-N escitalopram Chemical compound C1([C@]2(C3=CC=C(C=C3CO2)C#N)CCCN(C)C)=CC=C(F)C=C1 WSEQXVZVJXJVFP-FQEVSTJZSA-N 0.000 claims description 2
- 229960002336 estazolam Drugs 0.000 claims description 2
- CDCHDCWJMGXXRH-UHFFFAOYSA-N estazolam Chemical compound C=1C(Cl)=CC=C(N2C=NN=C2CN=2)C=1C=2C1=CC=CC=C1 CDCHDCWJMGXXRH-UHFFFAOYSA-N 0.000 claims description 2
- PYGWGZALEOIKDF-UHFFFAOYSA-N etravirine Chemical compound CC1=CC(C#N)=CC(C)=C1OC1=NC(NC=2C=CC(=CC=2)C#N)=NC(N)=C1Br PYGWGZALEOIKDF-UHFFFAOYSA-N 0.000 claims description 2
- 229960002049 etravirine Drugs 0.000 claims description 2
- 208000030533 eye disease Diseases 0.000 claims description 2
- 229960000815 ezetimibe Drugs 0.000 claims description 2
- OLNTVTPDXPETLC-XPWALMASSA-N ezetimibe Chemical compound N1([C@@H]([C@H](C1=O)CC[C@H](O)C=1C=CC(F)=CC=1)C=1C=CC(O)=CC=1)C1=CC=C(F)C=C1 OLNTVTPDXPETLC-XPWALMASSA-N 0.000 claims description 2
- 229960004396 famciclovir Drugs 0.000 claims description 2
- GGXKWVWZWMLJEH-UHFFFAOYSA-N famcyclovir Chemical compound N1=C(N)N=C2N(CCC(COC(=O)C)COC(C)=O)C=NC2=C1 GGXKWVWZWMLJEH-UHFFFAOYSA-N 0.000 claims description 2
- 229960003580 felodipine Drugs 0.000 claims description 2
- 229960002297 fenofibrate Drugs 0.000 claims description 2
- YMTINGFKWWXKFG-UHFFFAOYSA-N fenofibrate Chemical compound C1=CC(OC(C)(C)C(=O)OC(C)C)=CC=C1C(=O)C1=CC=C(Cl)C=C1 YMTINGFKWWXKFG-UHFFFAOYSA-N 0.000 claims description 2
- 229960001419 fenoprofen Drugs 0.000 claims description 2
- 229960003024 fenpiprane Drugs 0.000 claims description 2
- JXJPYHDHJZJWRI-UHFFFAOYSA-N fenpiprane Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)CCN1CCCCC1 JXJPYHDHJZJWRI-UHFFFAOYSA-N 0.000 claims description 2
- 229960001651 fentonium Drugs 0.000 claims description 2
- CSYZZFNWCDOVIM-OCTNZTSRSA-N fentonium Chemical compound C[N+]1(CC(=O)C2=CC=C(C=C2)C2=CC=CC=C2)[C@H]2CC[C@@H]1C[C@@H](C2)OC(=O)[C@H](CO)C1=CC=CC=C1 CSYZZFNWCDOVIM-OCTNZTSRSA-N 0.000 claims description 2
- 239000003527 fibrinolytic agent Substances 0.000 claims description 2
- 230000003480 fibrinolytic effect Effects 0.000 claims description 2
- 229960003670 flecainide acetate Drugs 0.000 claims description 2
- 229960004273 floxacillin Drugs 0.000 claims description 2
- RFHAOTPXVQNOHP-UHFFFAOYSA-N fluconazole Chemical compound C1=NC=NN1CC(C=1C(=CC(F)=CC=1)F)(O)CN1C=NC=N1 RFHAOTPXVQNOHP-UHFFFAOYSA-N 0.000 claims description 2
- 229960004884 fluconazole Drugs 0.000 claims description 2
- 229960000390 fludarabine Drugs 0.000 claims description 2
- GIUYCYHIANZCFB-FJFJXFQQSA-N fludarabine phosphate Chemical compound C1=NC=2C(N)=NC(F)=NC=2N1[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@@H]1O GIUYCYHIANZCFB-FJFJXFQQSA-N 0.000 claims description 2
- 229960002464 fluoxetine Drugs 0.000 claims description 2
- 229960003528 flurazepam Drugs 0.000 claims description 2
- SAADBVWGJQAEFS-UHFFFAOYSA-N flurazepam Chemical compound N=1CC(=O)N(CCN(CC)CC)C2=CC=C(Cl)C=C2C=1C1=CC=CC=C1F SAADBVWGJQAEFS-UHFFFAOYSA-N 0.000 claims description 2
- 229960002390 flurbiprofen Drugs 0.000 claims description 2
- SYTBZMRGLBWNTM-UHFFFAOYSA-N flurbiprofen Chemical compound FC1=CC(C(C(O)=O)C)=CC=C1C1=CC=CC=C1 SYTBZMRGLBWNTM-UHFFFAOYSA-N 0.000 claims description 2
- 229960003765 fluvastatin Drugs 0.000 claims description 2
- 229960004038 fluvoxamine Drugs 0.000 claims description 2
- CJOFXWAVKWHTFT-XSFVSMFZSA-N fluvoxamine Chemical compound COCCCC\C(=N/OCCN)C1=CC=C(C(F)(F)F)C=C1 CJOFXWAVKWHTFT-XSFVSMFZSA-N 0.000 claims description 2
- BPZSYCZIITTYBL-UHFFFAOYSA-N formoterol Chemical compound C1=CC(OC)=CC=C1CC(C)NCC(O)C1=CC=C(O)C(NC=O)=C1 BPZSYCZIITTYBL-UHFFFAOYSA-N 0.000 claims description 2
- 229960002848 formoterol Drugs 0.000 claims description 2
- 229960002490 fosinopril Drugs 0.000 claims description 2
- 229960003883 furosemide Drugs 0.000 claims description 2
- 229960004675 fusidic acid Drugs 0.000 claims description 2
- IECPWNUMDGFDKC-MZJAQBGESA-N fusidic acid Chemical compound O[C@@H]([C@@H]12)C[C@H]3\C(=C(/CCC=C(C)C)C(O)=O)[C@@H](OC(C)=O)C[C@]3(C)[C@@]2(C)CC[C@@H]2[C@]1(C)CC[C@@H](O)[C@H]2C IECPWNUMDGFDKC-MZJAQBGESA-N 0.000 claims description 2
- 229960003980 galantamine Drugs 0.000 claims description 2
- ASUTZQLVASHGKV-UHFFFAOYSA-N galanthamine hydrochloride Natural products O1C(=C23)C(OC)=CC=C2CN(C)CCC23C1CC(O)C=C2 ASUTZQLVASHGKV-UHFFFAOYSA-N 0.000 claims description 2
- 230000002496 gastric effect Effects 0.000 claims description 2
- 229960003627 gemfibrozil Drugs 0.000 claims description 2
- 229960002518 gentamicin Drugs 0.000 claims description 2
- 206010061989 glomerulosclerosis Diseases 0.000 claims description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 claims description 2
- 229960003711 glyceryl trinitrate Drugs 0.000 claims description 2
- 201000003872 goiter Diseases 0.000 claims description 2
- 208000007475 hemolytic anemia Diseases 0.000 claims description 2
- 208000014617 hemorrhoid Diseases 0.000 claims description 2
- 208000006454 hepatitis Diseases 0.000 claims description 2
- 231100000283 hepatitis Toxicity 0.000 claims description 2
- 229960001666 hexocyclium Drugs 0.000 claims description 2
- 229960002474 hydralazine Drugs 0.000 claims description 2
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 2
- 229960001545 hydrotalcite Drugs 0.000 claims description 2
- 229910001701 hydrotalcite Inorganic materials 0.000 claims description 2
- 201000001421 hyperglycemia Diseases 0.000 claims description 2
- 208000033066 hyperinsulinemic hypoglycemia Diseases 0.000 claims description 2
- 201000008980 hyperinsulinism Diseases 0.000 claims description 2
- 230000002218 hypoglycaemic effect Effects 0.000 claims description 2
- 208000003532 hypothyroidism Diseases 0.000 claims description 2
- 230000002989 hypothyroidism Effects 0.000 claims description 2
- 229960001680 ibuprofen Drugs 0.000 claims description 2
- 229960000908 idarubicin Drugs 0.000 claims description 2
- 208000008384 ileus Diseases 0.000 claims description 2
- 229960002240 iloprost Drugs 0.000 claims description 2
- HIFJCPQKFCZDDL-ACWOEMLNSA-N iloprost Chemical compound C1\C(=C/CCCC(O)=O)C[C@@H]2[C@@H](/C=C/[C@@H](O)C(C)CC#CC)[C@H](O)C[C@@H]21 HIFJCPQKFCZDDL-ACWOEMLNSA-N 0.000 claims description 2
- 229960001195 imidapril Drugs 0.000 claims description 2
- KLZWOWYOHUKJIG-BPUTZDHNSA-N imidapril Chemical compound C([C@@H](C(=O)OCC)N[C@@H](C)C(=O)N1C(N(C)C[C@H]1C(O)=O)=O)CC1=CC=CC=C1 KLZWOWYOHUKJIG-BPUTZDHNSA-N 0.000 claims description 2
- 229960002182 imipenem Drugs 0.000 claims description 2
- ZSKVGTPCRGIANV-ZXFLCMHBSA-N imipenem Chemical compound C1C(SCC\N=C\N)=C(C(O)=O)N2C(=O)[C@H]([C@H](O)C)[C@H]21 ZSKVGTPCRGIANV-ZXFLCMHBSA-N 0.000 claims description 2
- 229960004801 imipramine Drugs 0.000 claims description 2
- BCGWQEUPMDMJNV-UHFFFAOYSA-N imipramine Chemical compound C1CC2=CC=CC=C2N(CCCN(C)C)C2=CC=CC=C21 BCGWQEUPMDMJNV-UHFFFAOYSA-N 0.000 claims description 2
- 230000028993 immune response Effects 0.000 claims description 2
- 201000001881 impotence Diseases 0.000 claims description 2
- 208000027866 inflammatory disease Diseases 0.000 claims description 2
- 230000002757 inflammatory effect Effects 0.000 claims description 2
- 206010022000 influenza Diseases 0.000 claims description 2
- 229960005436 inositol nicotinate Drugs 0.000 claims description 2
- 229950000038 interferon alfa Drugs 0.000 claims description 2
- 208000036971 interstitial lung disease 2 Diseases 0.000 claims description 2
- 208000001286 intracranial vasospasm Diseases 0.000 claims description 2
- 201000004614 iritis Diseases 0.000 claims description 2
- 229960001737 isopropamide Drugs 0.000 claims description 2
- 229960000201 isosorbide dinitrate Drugs 0.000 claims description 2
- MOYKHGMNXAOIAT-JGWLITMVSA-N isosorbide dinitrate Chemical compound [O-][N+](=O)O[C@H]1CO[C@@H]2[C@H](O[N+](=O)[O-])CO[C@@H]21 MOYKHGMNXAOIAT-JGWLITMVSA-N 0.000 claims description 2
- 229960003827 isosorbide mononitrate Drugs 0.000 claims description 2
- YWXYYJSYQOXTPL-SLPGGIOYSA-N isosorbide mononitrate Chemical compound [O-][N+](=O)O[C@@H]1CO[C@@H]2[C@@H](O)CO[C@@H]21 YWXYYJSYQOXTPL-SLPGGIOYSA-N 0.000 claims description 2
- 229960004427 isradipine Drugs 0.000 claims description 2
- 229960004125 ketoconazole Drugs 0.000 claims description 2
- 229960004340 lacidipine Drugs 0.000 claims description 2
- GKQPCPXONLDCMU-CCEZHUSRSA-N lacidipine Chemical compound CCOC(=O)C1=C(C)NC(C)=C(C(=O)OCC)C1C1=CC=CC=C1\C=C\C(=O)OC(C)(C)C GKQPCPXONLDCMU-CCEZHUSRSA-N 0.000 claims description 2
- 229960001627 lamivudine Drugs 0.000 claims description 2
- JTEGQNOMFQHVDC-NKWVEPMBSA-N lamivudine Chemical compound O=C1N=C(N)C=CN1[C@H]1O[C@@H](CO)SC1 JTEGQNOMFQHVDC-NKWVEPMBSA-N 0.000 claims description 2
- 229960004408 lepirudin Drugs 0.000 claims description 2
- OTQCKZUSUGYWBD-BRHMIFOHSA-N lepirudin Chemical compound C([C@@H](C(=O)N[C@H](C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CS)C(=O)N[C@H](C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CS)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CS)C(=O)N[C@@H](CCC(O)=O)C(=O)NCC(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@H](C(=O)N[C@@H](CS)C(=O)NCC(=O)N[C@@H](CCC(N)=O)C(=O)NCC(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CS)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N[C@@H](CO)C(=O)N[C@@H](CC(O)=O)C(=O)NCC(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CS)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H]([C@@H](C)O)C(=O)NCC(=O)N[C@@H](CCC(O)=O)C(=O)NCC(=O)N[C@@H]([C@@H](C)O)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCCCN)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC=1NC=NC=1)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)NCC(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(O)=O)C(C)C)[C@@H](C)O)[C@@H](C)O)NC(=O)[C@@H](NC(=O)[C@@H](N)CC(C)C)[C@@H](C)O)C1=CC=C(O)C=C1 OTQCKZUSUGYWBD-BRHMIFOHSA-N 0.000 claims description 2
- 229960004294 lercanidipine Drugs 0.000 claims description 2
- ZDXUKAKRHYTAKV-UHFFFAOYSA-N lercanidipine Chemical compound COC(=O)C1=C(C)NC(C)=C(C(=O)OC(C)(C)CN(C)CCC(C=2C=CC=CC=2)C=2C=CC=CC=2)C1C1=CC=CC([N+]([O-])=O)=C1 ZDXUKAKRHYTAKV-UHFFFAOYSA-N 0.000 claims description 2
- 229960004502 levodopa Drugs 0.000 claims description 2
- 229960003376 levofloxacin Drugs 0.000 claims description 2
- 229960003907 linezolid Drugs 0.000 claims description 2
- TYZROVQLWOKYKF-ZDUSSCGKSA-N linezolid Chemical compound O=C1O[C@@H](CNC(=O)C)CN1C(C=C1F)=CC=C1N1CCOCC1 TYZROVQLWOKYKF-ZDUSSCGKSA-N 0.000 claims description 2
- 229960002394 lisinopril Drugs 0.000 claims description 2
- RLAWWYSOJDYHDC-BZSNNMDCSA-N lisinopril Chemical compound C([C@H](N[C@@H](CCCCN)C(=O)N1[C@@H](CCC1)C(O)=O)C(O)=O)CC1=CC=CC=C1 RLAWWYSOJDYHDC-BZSNNMDCSA-N 0.000 claims description 2
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 claims description 2
- 229910052808 lithium carbonate Inorganic materials 0.000 claims description 2
- 229940008015 lithium carbonate Drugs 0.000 claims description 2
- 229940071264 lithium citrate Drugs 0.000 claims description 2
- WJSIUCDMWSDDCE-UHFFFAOYSA-K lithium citrate (anhydrous) Chemical compound [Li+].[Li+].[Li+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O WJSIUCDMWSDDCE-UHFFFAOYSA-K 0.000 claims description 2
- 201000007270 liver cancer Diseases 0.000 claims description 2
- 208000019423 liver disease Diseases 0.000 claims description 2
- 208000014018 liver neoplasm Diseases 0.000 claims description 2
- 229960005209 lofexidine Drugs 0.000 claims description 2
- KSMAGQUYOIHWFS-UHFFFAOYSA-N lofexidine Chemical compound N=1CCNC=1C(C)OC1=C(Cl)C=CC=C1Cl KSMAGQUYOIHWFS-UHFFFAOYSA-N 0.000 claims description 2
- UTEFBSAVJNEPTR-RGEXLXHISA-N loprazolam Chemical compound C1CN(C)CCN1\C=C/1C(=O)N2C3=CC=C([N+]([O-])=O)C=C3C(C=3C(=CC=CC=3)Cl)=NCC2=N\1 UTEFBSAVJNEPTR-RGEXLXHISA-N 0.000 claims description 2
- 229960003019 loprazolam Drugs 0.000 claims description 2
- 229960004033 lormetazepam Drugs 0.000 claims description 2
- 201000005202 lung cancer Diseases 0.000 claims description 2
- 208000020816 lung neoplasm Diseases 0.000 claims description 2
- 206010025135 lupus erythematosus Diseases 0.000 claims description 2
- 201000010230 macular retinal edema Diseases 0.000 claims description 2
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 claims description 2
- 239000001095 magnesium carbonate Substances 0.000 claims description 2
- 229910000021 magnesium carbonate Inorganic materials 0.000 claims description 2
- 239000000391 magnesium silicate Substances 0.000 claims description 2
- 229940099273 magnesium trisilicate Drugs 0.000 claims description 2
- 229910000386 magnesium trisilicate Inorganic materials 0.000 claims description 2
- 235000019793 magnesium trisilicate Nutrition 0.000 claims description 2
- 208000027202 mammary Paget disease Diseases 0.000 claims description 2
- 229960003439 mebendazole Drugs 0.000 claims description 2
- BAXLBXFAUKGCDY-UHFFFAOYSA-N mebendazole Chemical compound [CH]1C2=NC(NC(=O)OC)=NC2=CC=C1C(=O)C1=CC=CC=C1 BAXLBXFAUKGCDY-UHFFFAOYSA-N 0.000 claims description 2
- 229960003577 mebeverine Drugs 0.000 claims description 2
- 238000002483 medication Methods 0.000 claims description 2
- BUGYDGFZZOZRHP-UHFFFAOYSA-N memantine Chemical compound C1C(C2)CC3(C)CC1(C)CC2(N)C3 BUGYDGFZZOZRHP-UHFFFAOYSA-N 0.000 claims description 2
- 229960004640 memantine Drugs 0.000 claims description 2
- 229960000901 mepacrine Drugs 0.000 claims description 2
- 229960003092 mepenzolate Drugs 0.000 claims description 2
- 229960002260 meropenem Drugs 0.000 claims description 2
- DMJNNHOOLUXYBV-PQTSNVLCSA-N meropenem Chemical compound C=1([C@H](C)[C@@H]2[C@H](C(N2C=1C(O)=O)=O)[C@H](O)C)S[C@@H]1CN[C@H](C(=O)N(C)C)C1 DMJNNHOOLUXYBV-PQTSNVLCSA-N 0.000 claims description 2
- KBOPZPXVLCULAV-UHFFFAOYSA-N mesalamine Chemical compound NC1=CC=C(O)C(C(O)=O)=C1 KBOPZPXVLCULAV-UHFFFAOYSA-N 0.000 claims description 2
- 229960004963 mesalazine Drugs 0.000 claims description 2
- 208000030159 metabolic disease Diseases 0.000 claims description 2
- 229960003663 metaraminol Drugs 0.000 claims description 2
- 229960003900 methenamine hippurate Drugs 0.000 claims description 2
- 229940042053 methotrimeprazine Drugs 0.000 claims description 2
- VRQVVMDWGGWHTJ-CQSZACIVSA-N methotrimeprazine Chemical compound C1=CC=C2N(C[C@H](C)CN(C)C)C3=CC(OC)=CC=C3SC2=C1 VRQVVMDWGGWHTJ-CQSZACIVSA-N 0.000 claims description 2
- 229960005096 methylatropine Drugs 0.000 claims description 2
- PIPAJLPNWZMYQA-YVSFHVDLSA-N methylatropine Chemical compound C[N+]1(C)[C@@H]2CC[C@H]1C[C@@H](C2)OC(=O)[C@@H](CO)c3ccccc3 PIPAJLPNWZMYQA-YVSFHVDLSA-N 0.000 claims description 2
- 229960004584 methylprednisolone Drugs 0.000 claims description 2
- 229960004503 metoclopramide Drugs 0.000 claims description 2
- TTWJBBZEZQICBI-UHFFFAOYSA-N metoclopramide Chemical compound CCN(CC)CCNC(=O)C1=CC(Cl)=C(N)C=C1OC TTWJBBZEZQICBI-UHFFFAOYSA-N 0.000 claims description 2
- 229960001300 metoprolol tartrate Drugs 0.000 claims description 2
- 229960000282 metronidazole Drugs 0.000 claims description 2
- VAOCPAMSLUNLGC-UHFFFAOYSA-N metronidazole Chemical compound CC1=NC=C([N+]([O-])=O)N1CCO VAOCPAMSLUNLGC-UHFFFAOYSA-N 0.000 claims description 2
- 229960002159 micafungin Drugs 0.000 claims description 2
- PIEUQSKUWLMALL-YABMTYFHSA-N micafungin Chemical compound C1=CC(OCCCCC)=CC=C1C1=CC(C=2C=CC(=CC=2)C(=O)N[C@@H]2C(N[C@H](C(=O)N3C[C@H](O)C[C@H]3C(=O)N[C@H](C(=O)N[C@H](C(=O)N3C[C@H](C)[C@H](O)[C@H]3C(=O)N[C@H](O)[C@H](O)C2)[C@H](O)CC(N)=O)[C@H](O)[C@@H](O)C=2C=C(OS(O)(=O)=O)C(O)=CC=2)[C@@H](C)O)=O)=NO1 PIEUQSKUWLMALL-YABMTYFHSA-N 0.000 claims description 2
- 239000004200 microcrystalline wax Substances 0.000 claims description 2
- 235000019808 microcrystalline wax Nutrition 0.000 claims description 2
- 229960003574 milrinone Drugs 0.000 claims description 2
- PZRHRDRVRGEVNW-UHFFFAOYSA-N milrinone Chemical compound N1C(=O)C(C#N)=CC(C=2C=CN=CC=2)=C1C PZRHRDRVRGEVNW-UHFFFAOYSA-N 0.000 claims description 2
- 229960004023 minocycline Drugs 0.000 claims description 2
- 229960003632 minoxidil Drugs 0.000 claims description 2
- 229960001785 mirtazapine Drugs 0.000 claims description 2
- RONZAEMNMFQXRA-UHFFFAOYSA-N mirtazapine Chemical compound C1C2=CC=CN=C2N2CCN(C)CC2C2=CC=CC=C21 RONZAEMNMFQXRA-UHFFFAOYSA-N 0.000 claims description 2
- 229960005249 misoprostol Drugs 0.000 claims description 2
- 229960004857 mitomycin Drugs 0.000 claims description 2
- KKZJGLLVHKMTCM-UHFFFAOYSA-N mitoxantrone Chemical compound O=C1C2=C(O)C=CC(O)=C2C(=O)C2=C1C(NCCNCCO)=CC=C2NCCNCCO KKZJGLLVHKMTCM-UHFFFAOYSA-N 0.000 claims description 2
- 229960001156 mitoxantrone Drugs 0.000 claims description 2
- 229960005170 moexipril Drugs 0.000 claims description 2
- 229960005127 montelukast Drugs 0.000 claims description 2
- FABPRXSRWADJSP-MEDUHNTESA-N moxifloxacin Chemical compound COC1=C(N2C[C@H]3NCCC[C@H]3C2)C(F)=CC(C(C(C(O)=O)=C2)=O)=C1N2C1CC1 FABPRXSRWADJSP-MEDUHNTESA-N 0.000 claims description 2
- 229960003702 moxifloxacin Drugs 0.000 claims description 2
- 208000001725 mucocutaneous lymph node syndrome Diseases 0.000 claims description 2
- 201000006417 multiple sclerosis Diseases 0.000 claims description 2
- 206010028417 myasthenia gravis Diseases 0.000 claims description 2
- MFZCIDXOLLEMOO-GYSGTQPESA-N myo-inositol hexanicotinate Chemical compound O([C@H]1[C@@H]([C@H]([C@@H](OC(=O)C=2C=NC=CC=2)[C@@H](OC(=O)C=2C=NC=CC=2)[C@@H]1OC(=O)C=1C=NC=CC=1)OC(=O)C=1C=NC=CC=1)OC(=O)C=1C=NC=CC=1)C(=O)C1=CC=CN=C1 MFZCIDXOLLEMOO-GYSGTQPESA-N 0.000 claims description 2
- 230000002107 myocardial effect Effects 0.000 claims description 2
- JORAUNFTUVJTNG-BSTBCYLQSA-N n-[(2s)-4-amino-1-[[(2s,3r)-1-[[(2s)-4-amino-1-oxo-1-[[(3s,6s,9s,12s,15r,18s,21s)-6,9,18-tris(2-aminoethyl)-3-[(1r)-1-hydroxyethyl]-12,15-bis(2-methylpropyl)-2,5,8,11,14,17,20-heptaoxo-1,4,7,10,13,16,19-heptazacyclotricos-21-yl]amino]butan-2-yl]amino]-3-h Chemical compound CC(C)CCCCC(=O)N[C@@H](CCN)C(=O)N[C@H]([C@@H](C)O)CN[C@@H](CCN)C(=O)N[C@H]1CCNC(=O)[C@H]([C@@H](C)O)NC(=O)[C@H](CCN)NC(=O)[C@H](CCN)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](CCN)NC1=O.CCC(C)CCCCC(=O)N[C@@H](CCN)C(=O)N[C@H]([C@@H](C)O)CN[C@@H](CCN)C(=O)N[C@H]1CCNC(=O)[C@H]([C@@H](C)O)NC(=O)[C@H](CCN)NC(=O)[C@H](CCN)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](CCN)NC1=O JORAUNFTUVJTNG-BSTBCYLQSA-N 0.000 claims description 2
- 229960004270 nabumetone Drugs 0.000 claims description 2
- 229960004255 nadolol Drugs 0.000 claims description 2
- VWPOSFSPZNDTMJ-UCWKZMIHSA-N nadolol Chemical compound C1[C@@H](O)[C@@H](O)CC2=C1C=CC=C2OCC(O)CNC(C)(C)C VWPOSFSPZNDTMJ-UCWKZMIHSA-N 0.000 claims description 2
- 229960001132 naftidrofuryl Drugs 0.000 claims description 2
- MHWLWQUZZRMNGJ-UHFFFAOYSA-N nalidixic acid Chemical compound C1=C(C)N=C2N(CC)C=C(C(O)=O)C(=O)C2=C1 MHWLWQUZZRMNGJ-UHFFFAOYSA-N 0.000 claims description 2
- 229960000210 nalidixic acid Drugs 0.000 claims description 2
- 201000003631 narcolepsy Diseases 0.000 claims description 2
- 229960000619 nebivolol Drugs 0.000 claims description 2
- 229960004927 neomycin Drugs 0.000 claims description 2
- 208000004296 neuralgia Diseases 0.000 claims description 2
- 230000004770 neurodegeneration Effects 0.000 claims description 2
- NQDJXKOVJZTUJA-UHFFFAOYSA-N nevirapine Chemical compound C12=NC=CC=C2C(=O)NC=2C(C)=CC=NC=2N1C1CC1 NQDJXKOVJZTUJA-UHFFFAOYSA-N 0.000 claims description 2
- 229960000689 nevirapine Drugs 0.000 claims description 2
- 229960001783 nicardipine Drugs 0.000 claims description 2
- HYIMSNHJOBLJNT-UHFFFAOYSA-N nifedipine Chemical compound COC(=O)C1=C(C)NC(C)=C(C(=O)OC)C1C1=CC=CC=C1[N+]([O-])=O HYIMSNHJOBLJNT-UHFFFAOYSA-N 0.000 claims description 2
- 229960001597 nifedipine Drugs 0.000 claims description 2
- 150000002823 nitrates Chemical class 0.000 claims description 2
- 229960001454 nitrazepam Drugs 0.000 claims description 2
- 229960000564 nitrofurantoin Drugs 0.000 claims description 2
- NXFQHRVNIOXGAQ-YCRREMRBSA-N nitrofurantoin Chemical compound O1C([N+](=O)[O-])=CC=C1\C=N\N1C(=O)NC(=O)C1 NXFQHRVNIOXGAQ-YCRREMRBSA-N 0.000 claims description 2
- 208000008338 non-alcoholic fatty liver disease Diseases 0.000 claims description 2
- 229960001158 nortriptyline Drugs 0.000 claims description 2
- 229960000988 nystatin Drugs 0.000 claims description 2
- VQOXZBDYSJBXMA-NQTDYLQESA-N nystatin A1 Chemical compound O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/CC/C=C/C=C/[C@H](C)[C@@H](O)[C@@H](C)[C@H](C)OC(=O)C[C@H](O)C[C@H](O)C[C@H](O)CC[C@@H](O)[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 VQOXZBDYSJBXMA-NQTDYLQESA-N 0.000 claims description 2
- 210000000056 organ Anatomy 0.000 claims description 2
- QVYRGXJJSLMXQH-UHFFFAOYSA-N orphenadrine Chemical compound C=1C=CC=C(C)C=1C(OCCN(C)C)C1=CC=CC=C1 QVYRGXJJSLMXQH-UHFFFAOYSA-N 0.000 claims description 2
- 229960003941 orphenadrine Drugs 0.000 claims description 2
- 230000003204 osmotic effect Effects 0.000 claims description 2
- 201000008482 osteoarthritis Diseases 0.000 claims description 2
- 229960000426 otilonium bromide Drugs 0.000 claims description 2
- VWZPIJGXYWHBOW-UHFFFAOYSA-N otilonium bromide Chemical compound [Br-].CCCCCCCCOC1=CC=CC=C1C(=O)NC1=CC=C(C(=O)OCC[N+](C)(CC)CC)C=C1 VWZPIJGXYWHBOW-UHFFFAOYSA-N 0.000 claims description 2
- 229960004570 oxprenolol Drugs 0.000 claims description 2
- LSQZJLSUYDQPKJ-UHFFFAOYSA-N p-Hydroxyampicillin Natural products O=C1N2C(C(O)=O)C(C)(C)SC2C1NC(=O)C(N)C1=CC=C(O)C=C1 LSQZJLSUYDQPKJ-UHFFFAOYSA-N 0.000 claims description 2
- 229960002296 paroxetine Drugs 0.000 claims description 2
- 230000007170 pathology Effects 0.000 claims description 2
- 235000019371 penicillin G benzathine Nutrition 0.000 claims description 2
- 229940056360 penicillin g Drugs 0.000 claims description 2
- 229940056367 penicillin v Drugs 0.000 claims description 2
- XDRYMKDFEDOLFX-UHFFFAOYSA-N pentamidine Chemical compound C1=CC(C(=N)N)=CC=C1OCCCCCOC1=CC=C(C(N)=N)C=C1 XDRYMKDFEDOLFX-UHFFFAOYSA-N 0.000 claims description 2
- 229960004448 pentamidine Drugs 0.000 claims description 2
- LUALIOATIOESLM-UHFFFAOYSA-N periciazine Chemical compound C1CC(O)CCN1CCCN1C2=CC(C#N)=CC=C2SC2=CC=CC=C21 LUALIOATIOESLM-UHFFFAOYSA-N 0.000 claims description 2
- 229960000769 periciazine Drugs 0.000 claims description 2
- 229960002582 perindopril Drugs 0.000 claims description 2
- IPVQLZZIHOAWMC-QXKUPLGCSA-N perindopril Chemical compound C1CCC[C@H]2C[C@@H](C(O)=O)N(C(=O)[C@H](C)N[C@@H](CCC)C(=O)OCC)[C@H]21 IPVQLZZIHOAWMC-QXKUPLGCSA-N 0.000 claims description 2
- 229960000762 perphenazine Drugs 0.000 claims description 2
- 229960000280 phenindione Drugs 0.000 claims description 2
- NFBAXHOPROOJAW-UHFFFAOYSA-N phenindione Chemical compound O=C1C2=CC=CC=C2C(=O)C1C1=CC=CC=C1 NFBAXHOPROOJAW-UHFFFAOYSA-N 0.000 claims description 2
- 229960002695 phenobarbital Drugs 0.000 claims description 2
- DDBREPKUVSBGFI-UHFFFAOYSA-N phenobarbital Chemical compound C=1C=CC=CC=1C1(CC)C(=O)NC(=O)NC1=O DDBREPKUVSBGFI-UHFFFAOYSA-N 0.000 claims description 2
- 229960003418 phenoxybenzamine Drugs 0.000 claims description 2
- BPLBGHOLXOTWMN-MBNYWOFBSA-N phenoxymethylpenicillin Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)COC1=CC=CC=C1 BPLBGHOLXOTWMN-MBNYWOFBSA-N 0.000 claims description 2
- 229960003056 phentolamine mesylate Drugs 0.000 claims description 2
- 229960002036 phenytoin Drugs 0.000 claims description 2
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 claims description 2
- 229960001553 phloroglucinol Drugs 0.000 claims description 2
- 239000002571 phosphodiesterase inhibitor Substances 0.000 claims description 2
- YVUQSNJEYSNKRX-UHFFFAOYSA-N pimozide Chemical compound C1=CC(F)=CC=C1C(C=1C=CC(F)=CC=1)CCCN1CCC(N2C(NC3=CC=CC=C32)=O)CC1 YVUQSNJEYSNKRX-UHFFFAOYSA-N 0.000 claims description 2
- 229960003634 pimozide Drugs 0.000 claims description 2
- 229960000361 pinaverium Drugs 0.000 claims description 2
- DDHUTBKXLWCZCO-UHFFFAOYSA-N pinaverium Chemical compound C1=C(OC)C(OC)=CC(Br)=C1C[N+]1(CCOCCC2C3CC(C3(C)C)CC2)CCOCC1 DDHUTBKXLWCZCO-UHFFFAOYSA-N 0.000 claims description 2
- 229960002508 pindolol Drugs 0.000 claims description 2
- PHUTUTUABXHXLW-UHFFFAOYSA-N pindolol Chemical compound CC(C)NCC(O)COC1=CC=CC2=NC=C[C]12 PHUTUTUABXHXLW-UHFFFAOYSA-N 0.000 claims description 2
- 229960005095 pioglitazone Drugs 0.000 claims description 2
- 229960001501 pipenzolate Drugs 0.000 claims description 2
- 229960002292 piperacillin Drugs 0.000 claims description 2
- 229960003033 piperidolate Drugs 0.000 claims description 2
- KTOYYUONFQWSMW-UHFFFAOYSA-N pipotiazine palmitate Chemical compound C1CC(CCOC(=O)CCCCCCCCCCCCCCC)CCN1CCCN1C2=CC(S(=O)(=O)N(C)C)=CC=C2SC2=CC=CC=C21 KTOYYUONFQWSMW-UHFFFAOYSA-N 0.000 claims description 2
- 229960004526 piracetam Drugs 0.000 claims description 2
- 239000000106 platelet aggregation inhibitor Substances 0.000 claims description 2
- 208000030428 polyarticular arthritis Diseases 0.000 claims description 2
- XDJYMJULXQKGMM-UHFFFAOYSA-N polymyxin E1 Natural products CCC(C)CCCCC(=O)NC(CCN)C(=O)NC(C(C)O)C(=O)NC(CCN)C(=O)NC1CCNC(=O)C(C(C)O)NC(=O)C(CCN)NC(=O)C(CCN)NC(=O)C(CC(C)C)NC(=O)C(CC(C)C)NC(=O)C(CCN)NC1=O XDJYMJULXQKGMM-UHFFFAOYSA-N 0.000 claims description 2
- KNIWPHSUTGNZST-UHFFFAOYSA-N polymyxin E2 Natural products CC(C)CCCCC(=O)NC(CCN)C(=O)NC(C(C)O)C(=O)NC(CCN)C(=O)NC1CCNC(=O)C(C(C)O)NC(=O)C(CCN)NC(=O)C(CCN)NC(=O)C(CC(C)C)NC(=O)C(CC(C)C)NC(=O)C(CCN)NC1=O KNIWPHSUTGNZST-UHFFFAOYSA-N 0.000 claims description 2
- 208000014081 polyp of colon Diseases 0.000 claims description 2
- 229920001296 polysiloxane Polymers 0.000 claims description 2
- 229960001589 posaconazole Drugs 0.000 claims description 2
- RAGOYPUPXAKGKH-XAKZXMRKSA-N posaconazole Chemical compound O=C1N([C@H]([C@H](C)O)CC)N=CN1C1=CC=C(N2CCN(CC2)C=2C=CC(OC[C@H]3C[C@@](CN4N=CN=C4)(OC3)C=3C(=CC(F)=CC=3)F)=CC=2)C=C1 RAGOYPUPXAKGKH-XAKZXMRKSA-N 0.000 claims description 2
- 239000003286 potassium sparing diuretic agent Substances 0.000 claims description 2
- 229940097241 potassium-sparing diuretic Drugs 0.000 claims description 2
- DWHGNUUWCJZQHO-ZVDZYBSKSA-M potassium;(2s,5r,6r)-6-[[(2r)-2-amino-2-(4-hydroxyphenyl)acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid;(2r,3z,5r)-3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]heptane-2-carboxylate Chemical compound [K+].[O-]C(=O)[C@H]1C(=C/CO)/O[C@@H]2CC(=O)N21.C1([C@@H](N)C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C(O)=O)(C)C)=CC=C(O)C=C1 DWHGNUUWCJZQHO-ZVDZYBSKSA-M 0.000 claims description 2
- 229960004197 prasugrel Drugs 0.000 claims description 2
- DTGLZDAWLRGWQN-UHFFFAOYSA-N prasugrel Chemical compound C1CC=2SC(OC(=O)C)=CC=2CN1C(C=1C(=CC=CC=1)F)C(=O)C1CC1 DTGLZDAWLRGWQN-UHFFFAOYSA-N 0.000 claims description 2
- 229960001289 prazosin Drugs 0.000 claims description 2
- IENZQIKPVFGBNW-UHFFFAOYSA-N prazosin Chemical compound N=1C(N)=C2C=C(OC)C(OC)=CC2=NC=1N(CC1)CCN1C(=O)C1=CC=CO1 IENZQIKPVFGBNW-UHFFFAOYSA-N 0.000 claims description 2
- 229960005205 prednisolone Drugs 0.000 claims description 2
- OIGNJSKKLXVSLS-VWUMJDOOSA-N prednisolone Chemical compound O=C1C=C[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 OIGNJSKKLXVSLS-VWUMJDOOSA-N 0.000 claims description 2
- 229960005275 prifinium bromide Drugs 0.000 claims description 2
- 229960002393 primidone Drugs 0.000 claims description 2
- DQMZLTXERSFNPB-UHFFFAOYSA-N primidone Chemical compound C=1C=CC=CC=1C1(CC)C(=O)NCNC1=O DQMZLTXERSFNPB-UHFFFAOYSA-N 0.000 claims description 2
- 229960003111 prochlorperazine Drugs 0.000 claims description 2
- WIKYUJGCLQQFNW-UHFFFAOYSA-N prochlorperazine Chemical compound C1CN(C)CCN1CCCN1C2=CC(Cl)=CC=C2SC2=CC=CC=C21 WIKYUJGCLQQFNW-UHFFFAOYSA-N 0.000 claims description 2
- 229960005253 procyclidine Drugs 0.000 claims description 2
- 229960005385 proguanil Drugs 0.000 claims description 2
- SSOLNOMRVKKSON-UHFFFAOYSA-N proguanil Chemical compound CC(C)\N=C(/N)N=C(N)NC1=CC=C(Cl)C=C1 SSOLNOMRVKKSON-UHFFFAOYSA-N 0.000 claims description 2
- 229960003598 promazine Drugs 0.000 claims description 2
- 229960002443 propafenone hydrochloride Drugs 0.000 claims description 2
- XWIHRGFIPXWGEF-UHFFFAOYSA-N propafenone hydrochloride Chemical compound Cl.CCCNCC(O)COC1=CC=CC=C1C(=O)CCC1=CC=CC=C1 XWIHRGFIPXWGEF-UHFFFAOYSA-N 0.000 claims description 2
- 229960000697 propantheline Drugs 0.000 claims description 2
- 229960005439 propantheline bromide Drugs 0.000 claims description 2
- 229940048914 protamine Drugs 0.000 claims description 2
- 229950008679 protamine sulfate Drugs 0.000 claims description 2
- 229940126409 proton pump inhibitor Drugs 0.000 claims description 2
- 239000000612 proton pump inhibitor Substances 0.000 claims description 2
- 229960001801 proxazole Drugs 0.000 claims description 2
- OLTAWOVKGWWERU-UHFFFAOYSA-N proxazole Chemical compound C=1C=CC=CC=1C(CC)C1=NOC(CCN(CC)CC)=N1 OLTAWOVKGWWERU-UHFFFAOYSA-N 0.000 claims description 2
- 208000002815 pulmonary hypertension Diseases 0.000 claims description 2
- 229960000611 pyrimethamine Drugs 0.000 claims description 2
- WKSAUQYGYAYLPV-UHFFFAOYSA-N pyrimethamine Chemical compound CCC1=NC(N)=NC(N)=C1C1=CC=C(Cl)C=C1 WKSAUQYGYAYLPV-UHFFFAOYSA-N 0.000 claims description 2
- 229960001964 quazepam Drugs 0.000 claims description 2
- 229960005197 quetiapine fumarate Drugs 0.000 claims description 2
- GPKJTRJOBQGKQK-UHFFFAOYSA-N quinacrine Chemical compound C1=C(OC)C=C2C(NC(C)CCCN(CC)CC)=C(C=CC(Cl)=C3)C3=NC2=C1 GPKJTRJOBQGKQK-UHFFFAOYSA-N 0.000 claims description 2
- 229960001455 quinapril Drugs 0.000 claims description 2
- JSDRRTOADPPCHY-HSQYWUDLSA-N quinapril Chemical compound C([C@@H](C(=O)OCC)N[C@@H](C)C(=O)N1[C@@H](CC2=CC=CC=C2C1)C(O)=O)CC1=CC=CC=C1 JSDRRTOADPPCHY-HSQYWUDLSA-N 0.000 claims description 2
- 229960000948 quinine Drugs 0.000 claims description 2
- 229960005442 quinupristin Drugs 0.000 claims description 2
- WTHRRGMBUAHGNI-LCYNINFDSA-N quinupristin Chemical compound N([C@@H]1C(=O)N[C@@H](C(N2CCC[C@H]2C(=O)N(C)[C@@H](CC=2C=CC(=CC=2)N(C)C)C(=O)N2C[C@@H](CS[C@H]3C4CCN(CC4)C3)C(=O)C[C@H]2C(=O)N[C@H](C(=O)O[C@@H]1C)C=1C=CC=CC=1)=O)CC)C(=O)C1=NC=CC=C1O WTHRRGMBUAHGNI-LCYNINFDSA-N 0.000 claims description 2
- 108700028429 quinupristin Proteins 0.000 claims description 2
- CZFFBEXEKNGXKS-UHFFFAOYSA-N raltegravir Chemical compound O1C(C)=NN=C1C(=O)NC(C)(C)C1=NC(C(=O)NCC=2C=CC(F)=CC=2)=C(O)C(=O)N1C CZFFBEXEKNGXKS-UHFFFAOYSA-N 0.000 claims description 2
- 229960004742 raltegravir Drugs 0.000 claims description 2
- 229960004432 raltitrexed Drugs 0.000 claims description 2
- 229960003401 ramipril Drugs 0.000 claims description 2
- HDACQVRGBOVJII-JBDAPHQKSA-N ramipril Chemical compound C([C@@H](C(=O)OCC)N[C@@H](C)C(=O)N1[C@@H](C[C@@H]2CCC[C@@H]21)C(O)=O)CC1=CC=CC=C1 HDACQVRGBOVJII-JBDAPHQKSA-N 0.000 claims description 2
- ZAHRKKWIAAJSAO-UHFFFAOYSA-N rapamycin Natural products COCC(O)C(=C/C(C)C(=O)CC(OC(=O)C1CCCCN1C(=O)C(=O)C2(O)OC(CC(OC)C(=CC=CC=CC(C)CC(C)C(=O)C)C)CCC2C)C(C)CC3CCC(O)C(C3)OC)C ZAHRKKWIAAJSAO-UHFFFAOYSA-N 0.000 claims description 2
- RUOKEQAAGRXIBM-GFCCVEGCSA-N rasagiline Chemical compound C1=CC=C2[C@H](NCC#C)CCC2=C1 RUOKEQAAGRXIBM-GFCCVEGCSA-N 0.000 claims description 2
- 229960000245 rasagiline Drugs 0.000 claims description 2
- 229960003770 reboxetine Drugs 0.000 claims description 2
- CBQGYUDMJHNJBX-RTBURBONSA-N reboxetine Chemical compound CCOC1=CC=CC=C1O[C@H](C=1C=CC=CC=1)[C@@H]1OCCNC1 CBQGYUDMJHNJBX-RTBURBONSA-N 0.000 claims description 2
- 238000010992 reflux Methods 0.000 claims description 2
- 201000010384 renal tubular acidosis Diseases 0.000 claims description 2
- 230000036454 renin-angiotensin system Effects 0.000 claims description 2
- 206010039083 rhinitis Diseases 0.000 claims description 2
- 229960001225 rifampicin Drugs 0.000 claims description 2
- JQXXHWHPUNPDRT-WLSIYKJHSA-N rifampicin Chemical compound O([C@](C1=O)(C)O/C=C/[C@@H]([C@H]([C@@H](OC(C)=O)[C@H](C)[C@H](O)[C@H](C)[C@@H](O)[C@@H](C)\C=C\C=C(C)/C(=O)NC=2C(O)=C3C([O-])=C4C)C)OC)C4=C1C3=C(O)C=2\C=N\N1CC[NH+](C)CC1 JQXXHWHPUNPDRT-WLSIYKJHSA-N 0.000 claims description 2
- 229960004181 riluzole Drugs 0.000 claims description 2
- 229960001534 risperidone Drugs 0.000 claims description 2
- RAPZEAPATHNIPO-UHFFFAOYSA-N risperidone Chemical compound FC1=CC=C2C(C3CCN(CC3)CCC=3C(=O)N4CCCCC4=NC=3C)=NOC2=C1 RAPZEAPATHNIPO-UHFFFAOYSA-N 0.000 claims description 2
- 229960001148 rivaroxaban Drugs 0.000 claims description 2
- KGFYHTZWPPHNLQ-AWEZNQCLSA-N rivaroxaban Chemical compound S1C(Cl)=CC=C1C(=O)NC[C@@H]1OC(=O)N(C=2C=CC(=CC=2)N2C(COCC2)=O)C1 KGFYHTZWPPHNLQ-AWEZNQCLSA-N 0.000 claims description 2
- 229960001879 ropinirole Drugs 0.000 claims description 2
- UHSKFQJFRQCDBE-UHFFFAOYSA-N ropinirole Chemical compound CCCN(CCC)CCC1=CC=CC2=C1CC(=O)N2 UHSKFQJFRQCDBE-UHFFFAOYSA-N 0.000 claims description 2
- 229960003179 rotigotine Drugs 0.000 claims description 2
- KFQYTPMOWPVWEJ-INIZCTEOSA-N rotigotine Chemical compound CCCN([C@@H]1CC2=CC=CC(O)=C2CC1)CCC1=CC=CS1 KFQYTPMOWPVWEJ-INIZCTEOSA-N 0.000 claims description 2
- 229960003014 rufinamide Drugs 0.000 claims description 2
- POGQSBRIGCQNEG-UHFFFAOYSA-N rufinamide Chemical compound N1=NC(C(=O)N)=CN1CC1=C(F)C=CC=C1F POGQSBRIGCQNEG-UHFFFAOYSA-N 0.000 claims description 2
- 229960001852 saquinavir Drugs 0.000 claims description 2
- QWAXKHKRTORLEM-UGJKXSETSA-N saquinavir Chemical compound C([C@@H]([C@H](O)CN1C[C@H]2CCCC[C@H]2C[C@H]1C(=O)NC(C)(C)C)NC(=O)[C@H](CC(N)=O)NC(=O)C=1N=C2C=CC=CC2=CC=1)C1=CC=CC=C1 QWAXKHKRTORLEM-UGJKXSETSA-N 0.000 claims description 2
- 208000005687 scabies Diseases 0.000 claims description 2
- 229960003946 selegiline Drugs 0.000 claims description 2
- 229960002073 sertraline Drugs 0.000 claims description 2
- VGKDLMBJGBXTGI-SJCJKPOMSA-N sertraline Chemical compound C1([C@@H]2CC[C@@H](C3=CC=CC=C32)NC)=CC=C(Cl)C(Cl)=C1 VGKDLMBJGBXTGI-SJCJKPOMSA-N 0.000 claims description 2
- 208000001050 sialadenitis Diseases 0.000 claims description 2
- 229960003310 sildenafil Drugs 0.000 claims description 2
- 229960003504 silicones Drugs 0.000 claims description 2
- 229960002855 simvastatin Drugs 0.000 claims description 2
- RYMZZMVNJRMUDD-HGQWONQESA-N simvastatin Chemical compound C([C@H]1[C@@H](C)C=CC2=C[C@H](C)C[C@@H]([C@H]12)OC(=O)C(C)(C)CC)C[C@@H]1C[C@@H](O)CC(=O)O1 RYMZZMVNJRMUDD-HGQWONQESA-N 0.000 claims description 2
- 229960002930 sirolimus Drugs 0.000 claims description 2
- QFJCIRLUMZQUOT-HPLJOQBZSA-N sirolimus Chemical compound C1C[C@@H](O)[C@H](OC)C[C@@H]1C[C@@H](C)[C@H]1OC(=O)[C@@H]2CCCCN2C(=O)C(=O)[C@](O)(O2)[C@H](C)CC[C@H]2C[C@H](OC)/C(C)=C/C=C/C=C/[C@@H](C)C[C@@H](C)C(=O)[C@H](OC)[C@H](O)/C(C)=C/[C@@H](C)C(=O)C1 QFJCIRLUMZQUOT-HPLJOQBZSA-N 0.000 claims description 2
- 229960002578 sitaxentan Drugs 0.000 claims description 2
- PHWXUGHIIBDVKD-UHFFFAOYSA-N sitaxentan Chemical compound CC1=NOC(NS(=O)(=O)C2=C(SC=C2)C(=O)CC=2C(=CC=3OCOC=3C=2)C)=C1Cl PHWXUGHIIBDVKD-UHFFFAOYSA-N 0.000 claims description 2
- 208000017520 skin disease Diseases 0.000 claims description 2
- 229940083542 sodium Drugs 0.000 claims description 2
- YQDGWZZYGYKDLR-UZVLBLASSA-K sodium stibogluconate Chemical compound O.O.O.O.O.O.O.O.O.[Na+].[Na+].[Na+].O1[C@H]([C@H](O)CO)[C@H](O2)[C@H](C([O-])=O)O[Sb]21([O-])O[Sb]1(O)(O[C@H]2C([O-])=O)O[C@H]([C@H](O)CO)[C@@H]2O1 YQDGWZZYGYKDLR-UZVLBLASSA-K 0.000 claims description 2
- 229960001567 sodium stibogluconate Drugs 0.000 claims description 2
- AEQFSUDEHCCHBT-UHFFFAOYSA-M sodium valproate Chemical compound [Na+].CCCC(C([O-])=O)CCC AEQFSUDEHCCHBT-UHFFFAOYSA-M 0.000 claims description 2
- 208000020431 spinal cord injury Diseases 0.000 claims description 2
- 229960002256 spironolactone Drugs 0.000 claims description 2
- LXMSZDCAJNLERA-ZHYRCANASA-N spironolactone Chemical compound C([C@@H]1[C@]2(C)CC[C@@H]3[C@@]4(C)CCC(=O)C=C4C[C@H]([C@@H]13)SC(=O)C)C[C@@]21CCC(=O)O1 LXMSZDCAJNLERA-ZHYRCANASA-N 0.000 claims description 2
- 201000005671 spondyloarthropathy Diseases 0.000 claims description 2
- 229960001203 stavudine Drugs 0.000 claims description 2
- 229930002534 steroid glycoside Natural products 0.000 claims description 2
- 150000008143 steroidal glycosides Chemical class 0.000 claims description 2
- 229960005322 streptomycin Drugs 0.000 claims description 2
- NCEXYHBECQHGNR-QZQOTICOSA-N sulfasalazine Chemical compound C1=C(O)C(C(=O)O)=CC(\N=N\C=2C=CC(=CC=2)S(=O)(=O)NC=2N=CC=CC=2)=C1 NCEXYHBECQHGNR-QZQOTICOSA-N 0.000 claims description 2
- 229960001940 sulfasalazine Drugs 0.000 claims description 2
- NCEXYHBECQHGNR-UHFFFAOYSA-N sulfasalazine Natural products C1=C(O)C(C(=O)O)=CC(N=NC=2C=CC(=CC=2)S(=O)(=O)NC=2N=CC=CC=2)=C1 NCEXYHBECQHGNR-UHFFFAOYSA-N 0.000 claims description 2
- 229960004940 sulpiride Drugs 0.000 claims description 2
- 229960001967 tacrolimus Drugs 0.000 claims description 2
- QJJXYPPXXYFBGM-SHYZHZOCSA-N tacrolimus Natural products CO[C@H]1C[C@H](CC[C@@H]1O)C=C(C)[C@H]2OC(=O)[C@H]3CCCCN3C(=O)C(=O)[C@@]4(O)O[C@@H]([C@H](C[C@H]4C)OC)[C@@H](C[C@H](C)CC(=C[C@@H](CC=C)C(=O)C[C@H](O)[C@H]2C)C)OC QJJXYPPXXYFBGM-SHYZHZOCSA-N 0.000 claims description 2
- IKBKZGMPCYNSLU-RGVLZGJSSA-N tegaserod Chemical compound C1=C(OC)C=C2C(/C=N/NC(=N)NCCCCC)=CNC2=C1 IKBKZGMPCYNSLU-RGVLZGJSSA-N 0.000 claims description 2
- 229960002876 tegaserod Drugs 0.000 claims description 2
- 229960001608 teicoplanin Drugs 0.000 claims description 2
- 229960003250 telithromycin Drugs 0.000 claims description 2
- LJVAJPDWBABPEJ-PNUFFHFMSA-N telithromycin Chemical compound O([C@@H]1[C@@H](C)C(=O)[C@@H](C)C(=O)O[C@@H]([C@]2(OC(=O)N(CCCCN3C=C(N=C3)C=3C=NC=CC=3)[C@@H]2[C@@H](C)C(=O)[C@H](C)C[C@@]1(C)OC)C)CC)[C@@H]1O[C@H](C)C[C@H](N(C)C)[C@H]1O LJVAJPDWBABPEJ-PNUFFHFMSA-N 0.000 claims description 2
- 229960005187 telmisartan Drugs 0.000 claims description 2
- 201000004415 tendinitis Diseases 0.000 claims description 2
- 229960001355 tenofovir disoproxil Drugs 0.000 claims description 2
- JFVZFKDSXNQEJW-CQSZACIVSA-N tenofovir disoproxil Chemical compound N1=CN=C2N(C[C@@H](C)OCP(=O)(OCOC(=O)OC(C)C)OCOC(=O)OC(C)C)C=NC2=C1N JFVZFKDSXNQEJW-CQSZACIVSA-N 0.000 claims description 2
- VCKUSRYTPJJLNI-UHFFFAOYSA-N terazosin Chemical compound N=1C(N)=C2C=C(OC)C(OC)=CC2=NC=1N(CC1)CCN1C(=O)C1CCCO1 VCKUSRYTPJJLNI-UHFFFAOYSA-N 0.000 claims description 2
- 229960001693 terazosin Drugs 0.000 claims description 2
- 229960002722 terbinafine Drugs 0.000 claims description 2
- DOMXUEMWDBAQBQ-WEVVVXLNSA-N terbinafine Chemical compound C1=CC=C2C(CN(C\C=C\C#CC(C)(C)C)C)=CC=CC2=C1 DOMXUEMWDBAQBQ-WEVVVXLNSA-N 0.000 claims description 2
- WUBVEMGCQRSBBT-UHFFFAOYSA-N tert-butyl 4-(trifluoromethylsulfonyloxy)-3,6-dihydro-2h-pyridine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCC(OS(=O)(=O)C(F)(F)F)=CC1 WUBVEMGCQRSBBT-UHFFFAOYSA-N 0.000 claims description 2
- 229960002180 tetracycline Drugs 0.000 claims description 2
- 229930101283 tetracycline Natural products 0.000 claims description 2
- 235000019364 tetracycline Nutrition 0.000 claims description 2
- 150000003522 tetracyclines Chemical class 0.000 claims description 2
- 239000003451 thiazide diuretic agent Substances 0.000 claims description 2
- 206010043778 thyroiditis Diseases 0.000 claims description 2
- 229960004659 ticarcillin Drugs 0.000 claims description 2
- OHKOGUYZJXTSFX-KZFFXBSXSA-N ticarcillin Chemical compound C=1([C@@H](C(O)=O)C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C(O)=O)(C)C)C=CSC=1 OHKOGUYZJXTSFX-KZFFXBSXSA-N 0.000 claims description 2
- 229960004089 tigecycline Drugs 0.000 claims description 2
- 229960003737 timepidium bromide Drugs 0.000 claims description 2
- 229960004605 timolol Drugs 0.000 claims description 2
- 229960005062 tinzaparin Drugs 0.000 claims description 2
- 229960003087 tioguanine Drugs 0.000 claims description 2
- MNRILEROXIRVNJ-UHFFFAOYSA-N tioguanine Chemical compound N1C(N)=NC(=S)C2=NC=N[C]21 MNRILEROXIRVNJ-UHFFFAOYSA-N 0.000 claims description 2
- 229960000838 tipranavir Drugs 0.000 claims description 2
- SUJUHGSWHZTSEU-FYBSXPHGSA-N tipranavir Chemical compound C([C@@]1(CCC)OC(=O)C([C@H](CC)C=2C=C(NS(=O)(=O)C=3N=CC(=CC=3)C(F)(F)F)C=CC=2)=C(O)C1)CC1=CC=CC=C1 SUJUHGSWHZTSEU-FYBSXPHGSA-N 0.000 claims description 2
- 229960003425 tirofiban Drugs 0.000 claims description 2
- COKMIXFXJJXBQG-NRFANRHFSA-N tirofiban Chemical compound C1=CC(C[C@H](NS(=O)(=O)CCCC)C(O)=O)=CC=C1OCCCCC1CCNCC1 COKMIXFXJJXBQG-NRFANRHFSA-N 0.000 claims description 2
- 229960000707 tobramycin Drugs 0.000 claims description 2
- NLVFBUXFDBBNBW-PBSUHMDJSA-N tobramycin Chemical compound N[C@@H]1C[C@H](O)[C@@H](CN)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O[C@@H]2[C@@H]([C@@H](N)[C@H](O)[C@@H](CO)O2)O)[C@H](N)C[C@@H]1N NLVFBUXFDBBNBW-PBSUHMDJSA-N 0.000 claims description 2
- 229960001017 tolmetin Drugs 0.000 claims description 2
- UPSPUYADGBWSHF-UHFFFAOYSA-N tolmetin Chemical compound C1=CC(C)=CC=C1C(=O)C1=CC=C(CC(O)=O)N1C UPSPUYADGBWSHF-UHFFFAOYSA-N 0.000 claims description 2
- 230000000699 topical effect Effects 0.000 claims description 2
- 229960004394 topiramate Drugs 0.000 claims description 2
- 229960005461 torasemide Drugs 0.000 claims description 2
- 229960004380 tramadol Drugs 0.000 claims description 2
- TVYLLZQTGLZFBW-GOEBONIOSA-N tramadol Natural products COC1=CC=CC([C@@]2(O)[C@@H](CCCC2)CN(C)C)=C1 TVYLLZQTGLZFBW-GOEBONIOSA-N 0.000 claims description 2
- 229960000401 tranexamic acid Drugs 0.000 claims description 2
- PHTUQLWOUWZIMZ-GZTJUZNOSA-N trans-dothiepin Chemical compound C1SC2=CC=CC=C2C(=C/CCN(C)C)/C2=CC=CC=C21 PHTUQLWOUWZIMZ-GZTJUZNOSA-N 0.000 claims description 2
- 229960005294 triamcinolone Drugs 0.000 claims description 2
- GFNANZIMVAIWHM-OBYCQNJPSA-N triamcinolone Chemical compound O=C1C=C[C@]2(C)[C@@]3(F)[C@@H](O)C[C@](C)([C@@]([C@H](O)C4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 GFNANZIMVAIWHM-OBYCQNJPSA-N 0.000 claims description 2
- 229960001288 triamterene Drugs 0.000 claims description 2
- 229960003386 triazolam Drugs 0.000 claims description 2
- JOFWLTCLBGQGBO-UHFFFAOYSA-N triazolam Chemical compound C12=CC(Cl)=CC=C2N2C(C)=NN=C2CN=C1C1=CC=CC=C1Cl JOFWLTCLBGQGBO-UHFFFAOYSA-N 0.000 claims description 2
- 229960002324 trifluoperazine Drugs 0.000 claims description 2
- ZEWQUBUPAILYHI-UHFFFAOYSA-N trifluoperazine Chemical compound C1CN(C)CCN1CCCN1C2=CC(C(F)(F)F)=CC=C2SC2=CC=CC=C21 ZEWQUBUPAILYHI-UHFFFAOYSA-N 0.000 claims description 2
- 201000008827 tuberculosis Diseases 0.000 claims description 2
- 208000025301 tympanitis Diseases 0.000 claims description 2
- 230000002485 urinary effect Effects 0.000 claims description 2
- 208000019206 urinary tract infection Diseases 0.000 claims description 2
- 229960001661 ursodiol Drugs 0.000 claims description 2
- 229940093257 valacyclovir Drugs 0.000 claims description 2
- 229940102566 valproate Drugs 0.000 claims description 2
- 229960000604 valproic acid Drugs 0.000 claims description 2
- 229960003165 vancomycin Drugs 0.000 claims description 2
- MYPYJXKWCTUITO-UHFFFAOYSA-N vancomycin Natural products O1C(C(=C2)Cl)=CC=C2C(O)C(C(NC(C2=CC(O)=CC(O)=C2C=2C(O)=CC=C3C=2)C(O)=O)=O)NC(=O)C3NC(=O)C2NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(CC(C)C)NC)C(O)C(C=C3Cl)=CC=C3OC3=CC2=CC1=C3OC1OC(CO)C(O)C(O)C1OC1CC(C)(N)C(O)C(C)O1 MYPYJXKWCTUITO-UHFFFAOYSA-N 0.000 claims description 2
- 229960001722 verapamil Drugs 0.000 claims description 2
- 229960005318 vigabatrin Drugs 0.000 claims description 2
- PJDFLNIOAUIZSL-UHFFFAOYSA-N vigabatrin Chemical compound C=CC(N)CCC(O)=O PJDFLNIOAUIZSL-UHFFFAOYSA-N 0.000 claims description 2
- 230000009385 viral infection Effects 0.000 claims description 2
- 230000008673 vomiting Effects 0.000 claims description 2
- BCEHBSKCWLPMDN-MGPLVRAMSA-N voriconazole Chemical compound C1([C@H](C)[C@](O)(CN2N=CN=C2)C=2C(=CC(F)=CC=2)F)=NC=NC=C1F BCEHBSKCWLPMDN-MGPLVRAMSA-N 0.000 claims description 2
- 229960004740 voriconazole Drugs 0.000 claims description 2
- 229960005080 warfarin Drugs 0.000 claims description 2
- PJVWKTKQMONHTI-UHFFFAOYSA-N warfarin Chemical compound OC=1C2=CC=CC=C2OC(=O)C=1C(CC(=O)C)C1=CC=CC=C1 PJVWKTKQMONHTI-UHFFFAOYSA-N 0.000 claims description 2
- 208000005494 xerophthalmia Diseases 0.000 claims description 2
- 229960000537 xipamide Drugs 0.000 claims description 2
- MTZBBNMLMNBNJL-UHFFFAOYSA-N xipamide Chemical compound CC1=CC=CC(C)=C1NC(=O)C1=CC(S(N)(=O)=O)=C(Cl)C=C1O MTZBBNMLMNBNJL-UHFFFAOYSA-N 0.000 claims description 2
- 229960000783 zuclopenthixol decanoate Drugs 0.000 claims description 2
- 208000034991 Hiatal Hernia Diseases 0.000 claims 2
- 206010020028 Hiatus hernia Diseases 0.000 claims 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims 2
- 208000024780 Urticaria Diseases 0.000 claims 2
- 125000005908 glyceryl ester group Chemical group 0.000 claims 2
- 229940127240 opiate Drugs 0.000 claims 2
- ZJAOAACCNHFJAH-UHFFFAOYSA-N phosphonoformic acid Chemical compound OC(=O)P(O)(O)=O ZJAOAACCNHFJAH-UHFFFAOYSA-N 0.000 claims 2
- 229910021653 sulphate ion Inorganic materials 0.000 claims 2
- FQXXSQDCDRQNQE-VMDGZTHMSA-N thebaine Chemical compound C([C@@H](N(CC1)C)C2=CC=C3OC)C4=CC=C(OC)C5=C4[C@@]21[C@H]3O5 FQXXSQDCDRQNQE-VMDGZTHMSA-N 0.000 claims 2
- XEEQGYMUWCZPDN-DOMZBBRYSA-N (-)-(11S,2'R)-erythro-mefloquine Chemical compound C([C@@H]1[C@@H](O)C=2C3=CC=CC(=C3N=C(C=2)C(F)(F)F)C(F)(F)F)CCCN1 XEEQGYMUWCZPDN-DOMZBBRYSA-N 0.000 claims 1
- FJLGEFLZQAZZCD-MCBHFWOFSA-N (3R,5S)-fluvastatin Chemical compound C12=CC=CC=C2N(C(C)C)C(\C=C\[C@@H](O)C[C@@H](O)CC(O)=O)=C1C1=CC=C(F)C=C1 FJLGEFLZQAZZCD-MCBHFWOFSA-N 0.000 claims 1
- GKNPSSNBBWDAGH-UHFFFAOYSA-N 2-hydroxy-2,2-diphenylacetic acid (1,1-dimethyl-3-piperidin-1-iumyl) ester Chemical compound C1[N+](C)(C)CCCC1OC(=O)C(O)(C=1C=CC=CC=1)C1=CC=CC=C1 GKNPSSNBBWDAGH-UHFFFAOYSA-N 0.000 claims 1
- VHRSUDSXCMQTMA-PJHHCJLFSA-N 6alpha-methylprednisolone Chemical compound C([C@@]12C)=CC(=O)C=C1[C@@H](C)C[C@@H]1[C@@H]2[C@@H](O)C[C@]2(C)[C@@](O)(C(=O)CO)CC[C@H]21 VHRSUDSXCMQTMA-PJHHCJLFSA-N 0.000 claims 1
- OIRDTQYFTABQOQ-KQYNXXCUSA-N Adenosine Natural products C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O OIRDTQYFTABQOQ-KQYNXXCUSA-N 0.000 claims 1
- 208000023328 Basedow disease Diseases 0.000 claims 1
- 206010006448 Bronchiolitis Diseases 0.000 claims 1
- 206010007882 Cellulitis Diseases 0.000 claims 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 claims 1
- VYFYYTLLBUKUHU-UHFFFAOYSA-N Dopamine Natural products NCCC1=CC=C(O)C(O)=C1 VYFYYTLLBUKUHU-UHFFFAOYSA-N 0.000 claims 1
- 241000282324 Felis Species 0.000 claims 1
- 208000012671 Gastrointestinal haemorrhages Diseases 0.000 claims 1
- HVYGXNYMNHSBGD-UHFFFAOYSA-N Idanpramine Chemical compound C1=CC(OC)=CC=C1C1(C=2C=CC(OC)=CC=2)C(=O)N(CCN2CCCCC2)C(=O)N1 HVYGXNYMNHSBGD-UHFFFAOYSA-N 0.000 claims 1
- 102000014150 Interferons Human genes 0.000 claims 1
- 108010050904 Interferons Proteins 0.000 claims 1
- 206010022714 Intestinal ulcer Diseases 0.000 claims 1
- 241000931046 Metadon Species 0.000 claims 1
- KBAFPSLPKGSANY-UHFFFAOYSA-N Naftidrofuryl Chemical compound C=1C=CC2=CC=CC=C2C=1CC(C(=O)OCCN(CC)CC)CC1CCCO1 KBAFPSLPKGSANY-UHFFFAOYSA-N 0.000 claims 1
- YYQRGCZGSFRBAM-UHFFFAOYSA-N Triclofos Chemical compound OP(O)(=O)OCC(Cl)(Cl)Cl YYQRGCZGSFRBAM-UHFFFAOYSA-N 0.000 claims 1
- 229960002054 acenocoumarol Drugs 0.000 claims 1
- VABCILAOYCMVPS-UHFFFAOYSA-N acenocoumarol Chemical compound OC=1C2=CC=CC=C2OC(=O)C=1C(CC(=O)C)C1=CC=C([N+]([O-])=O)C=C1 VABCILAOYCMVPS-UHFFFAOYSA-N 0.000 claims 1
- 229960001997 adefovir Drugs 0.000 claims 1
- 239000003741 agents affecting lipid metabolism Substances 0.000 claims 1
- 239000000556 agonist Substances 0.000 claims 1
- LTKVFMLMEYCWMK-UHFFFAOYSA-N amiloride hydrochloride dihydrate Chemical compound [H+].O.O.[Cl-].NC(=N)NC(=O)C1=NC(Cl)=C(N)N=C1N LTKVFMLMEYCWMK-UHFFFAOYSA-N 0.000 claims 1
- 208000007502 anemia Diseases 0.000 claims 1
- 239000005557 antagonist Substances 0.000 claims 1
- 239000004004 anti-anginal agent Substances 0.000 claims 1
- 229940082620 antifibrinolytics Drugs 0.000 claims 1
- 229940006138 antiglaucoma drug and miotics prostaglandin analogues Drugs 0.000 claims 1
- 239000003420 antiserotonin agent Substances 0.000 claims 1
- 235000013871 bee wax Nutrition 0.000 claims 1
- 239000012166 beeswax Substances 0.000 claims 1
- BNQDCRGUHNALGH-UHFFFAOYSA-N benserazide Chemical compound OCC(N)C(=O)NNCC1=CC=C(O)C(O)=C1O BNQDCRGUHNALGH-UHFFFAOYSA-N 0.000 claims 1
- 229960001034 bromopride Drugs 0.000 claims 1
- RRGUKTPIGVIEKM-UHFFFAOYSA-N cilostazol Chemical compound C=1C=C2NC(=O)CCC2=CC=1OCCCCC1=NN=NN1C1CCCCC1 RRGUKTPIGVIEKM-UHFFFAOYSA-N 0.000 claims 1
- 229960005132 cisapride Drugs 0.000 claims 1
- DCSUBABJRXZOMT-IRLDBZIGSA-N cisapride Chemical compound C([C@@H]([C@@H](CC1)NC(=O)C=2C(=CC(N)=C(Cl)C=2)OC)OC)N1CCCOC1=CC=C(F)C=C1 DCSUBABJRXZOMT-IRLDBZIGSA-N 0.000 claims 1
- DCSUBABJRXZOMT-UHFFFAOYSA-N cisapride Natural products C1CC(NC(=O)C=2C(=CC(N)=C(Cl)C=2)OC)C(OC)CN1CCCOC1=CC=C(F)C=C1 DCSUBABJRXZOMT-UHFFFAOYSA-N 0.000 claims 1
- 206010009887 colitis Diseases 0.000 claims 1
- 230000002183 duodenal effect Effects 0.000 claims 1
- 230000002526 effect on cardiovascular system Effects 0.000 claims 1
- KAQKFAOMNZTLHT-VVUHWYTRSA-N epoprostenol Chemical compound O1C(=CCCCC(O)=O)C[C@@H]2[C@@H](/C=C/[C@@H](O)CCCCC)[C@H](O)C[C@@H]21 KAQKFAOMNZTLHT-VVUHWYTRSA-N 0.000 claims 1
- 230000002550 fecal effect Effects 0.000 claims 1
- 229960005102 foscarnet Drugs 0.000 claims 1
- 208000030304 gastrointestinal bleeding Diseases 0.000 claims 1
- 241000411851 herbal medicine Species 0.000 claims 1
- 229960004972 idanpramine Drugs 0.000 claims 1
- 229960000476 inosine pranobex Drugs 0.000 claims 1
- PBJNZCQJMWVIRT-MDQYBHOLSA-N inosine pranobex Chemical compound CC(O)CN(C)C.CC(=O)NC1=CC=C(C(O)=O)C=C1.O[C@H]1[C@@H](O)[C@H](CO)O[C@@H]1N1C2=NC=NC(O)=C2N=C1 PBJNZCQJMWVIRT-MDQYBHOLSA-N 0.000 claims 1
- 229940079322 interferon Drugs 0.000 claims 1
- DKYWVDODHFEZIM-UHFFFAOYSA-N ketoprofen Chemical compound OC(=O)C(C)C1=CC=CC(C(=O)C=2C=CC=CC=2)=C1 DKYWVDODHFEZIM-UHFFFAOYSA-N 0.000 claims 1
- 229960000991 ketoprofen Drugs 0.000 claims 1
- 229960003174 lansoprazole Drugs 0.000 claims 1
- MJIHNNLFOKEZEW-UHFFFAOYSA-N lansoprazole Chemical compound CC1=C(OCC(F)(F)F)C=CN=C1CS(=O)C1=NC2=CC=CC=C2N1 MJIHNNLFOKEZEW-UHFFFAOYSA-N 0.000 claims 1
- 229960001571 loperamide Drugs 0.000 claims 1
- RDOIQAHITMMDAJ-UHFFFAOYSA-N loperamide Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(C(=O)N(C)C)CCN(CC1)CCC1(O)C1=CC=C(Cl)C=C1 RDOIQAHITMMDAJ-UHFFFAOYSA-N 0.000 claims 1
- 229960001962 mefloquine Drugs 0.000 claims 1
- WCNLCIJMFAJCPX-UHFFFAOYSA-N pethidine hydrochloride Chemical compound Cl.C=1C=CC=CC=1C1(C(=O)OCC)CCN(C)CC1 WCNLCIJMFAJCPX-UHFFFAOYSA-N 0.000 claims 1
- IVBHGBMCVLDMKU-GXNBUGAJSA-N piperacillin Chemical compound O=C1C(=O)N(CC)CCN1C(=O)N[C@H](C=1C=CC=CC=1)C(=O)N[C@@H]1C(=O)N2[C@@H](C(O)=O)C(C)(C)S[C@@H]21 IVBHGBMCVLDMKU-GXNBUGAJSA-N 0.000 claims 1
- 229960005141 piperazine Drugs 0.000 claims 1
- 229960005179 primaquine Drugs 0.000 claims 1
- INDBQLZJXZLFIT-UHFFFAOYSA-N primaquine Chemical compound N1=CC=CC2=CC(OC)=CC(NC(C)CCCN)=C21 INDBQLZJXZLFIT-UHFFFAOYSA-N 0.000 claims 1
- 239000004575 stone Substances 0.000 claims 1
- 229960001114 temocillin Drugs 0.000 claims 1
- BVCKFLJARNKCSS-DWPRYXJFSA-N temocillin Chemical compound N([C@]1(OC)C(N2[C@H](C(C)(C)S[C@@H]21)C(O)=O)=O)C(=O)C(C(O)=O)C=1C=CSC=1 BVCKFLJARNKCSS-DWPRYXJFSA-N 0.000 claims 1
- 229960001918 tiagabine Drugs 0.000 claims 1
- PBJUNZJWGZTSKL-MRXNPFEDSA-N tiagabine Chemical compound C1=CSC(C(=CCCN2C[C@@H](CCC2)C(O)=O)C2=C(C=CS2)C)=C1C PBJUNZJWGZTSKL-MRXNPFEDSA-N 0.000 claims 1
- 229960001147 triclofos Drugs 0.000 claims 1
- MYPYJXKWCTUITO-LYRMYLQWSA-N vancomycin Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=C2C=C3C=C1OC1=CC=C(C=C1Cl)[C@@H](O)[C@H](C(N[C@@H](CC(N)=O)C(=O)N[C@H]3C(=O)N[C@H]1C(=O)N[C@H](C(N[C@@H](C3=CC(O)=CC(O)=C3C=3C(O)=CC=C1C=3)C(O)=O)=O)[C@H](O)C1=CC=C(C(=C1)Cl)O2)=O)NC(=O)[C@@H](CC(C)C)NC)[C@H]1C[C@](C)(N)[C@H](O)[C@H](C)O1 MYPYJXKWCTUITO-LYRMYLQWSA-N 0.000 claims 1
- 238000009472 formulation Methods 0.000 abstract description 32
- 239000003795 chemical substances by application Substances 0.000 abstract description 20
- 238000011282 treatment Methods 0.000 abstract description 9
- 238000013461 design Methods 0.000 abstract description 2
- 239000003826 tablet Substances 0.000 description 37
- 239000010410 layer Substances 0.000 description 24
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 21
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 13
- 238000000034 method Methods 0.000 description 11
- 239000011521 glass Substances 0.000 description 10
- 239000008187 granular material Substances 0.000 description 10
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
- 239000000945 filler Substances 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 206010021639 Incontinence Diseases 0.000 description 4
- 239000003153 chemical reaction reagent Substances 0.000 description 4
- 239000000306 component Substances 0.000 description 4
- 238000007906 compression Methods 0.000 description 4
- 230000006835 compression Effects 0.000 description 4
- 238000004090 dissolution Methods 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 230000009467 reduction Effects 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 3
- 239000008280 blood Substances 0.000 description 3
- 210000004369 blood Anatomy 0.000 description 3
- 239000012792 core layer Substances 0.000 description 3
- 239000002702 enteric coating Substances 0.000 description 3
- 238000009505 enteric coating Methods 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 210000001035 gastrointestinal tract Anatomy 0.000 description 3
- 238000004128 high performance liquid chromatography Methods 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000000314 lubricant Substances 0.000 description 3
- 235000019359 magnesium stearate Nutrition 0.000 description 3
- 230000002265 prevention Effects 0.000 description 3
- 150000005846 sugar alcohols Chemical class 0.000 description 3
- 230000001225 therapeutic effect Effects 0.000 description 3
- 230000002618 waking effect Effects 0.000 description 3
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 2
- 239000002947 C09CA04 - Irbesartan Substances 0.000 description 2
- UGJMXCAKCUNAIE-UHFFFAOYSA-N Gabapentin Chemical compound OC(=O)CC1(CN)CCCCC1 UGJMXCAKCUNAIE-UHFFFAOYSA-N 0.000 description 2
- 208000035895 Guillain-Barré syndrome Diseases 0.000 description 2
- RKUNBYITZUJHSG-UHFFFAOYSA-N Hyosciamin-hydrochlorid Natural products CN1C(C2)CCC1CC2OC(=O)C(CO)C1=CC=CC=C1 RKUNBYITZUJHSG-UHFFFAOYSA-N 0.000 description 2
- YJPIGAIKUZMOQA-UHFFFAOYSA-N Melatonin Natural products COC1=CC=C2N(C(C)=O)C=C(CCN)C2=C1 YJPIGAIKUZMOQA-UHFFFAOYSA-N 0.000 description 2
- 206010049567 Miller Fisher syndrome Diseases 0.000 description 2
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 description 2
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 229940049706 benzodiazepine Drugs 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000000872 buffer Substances 0.000 description 2
- 238000005119 centrifugation Methods 0.000 description 2
- 229960001259 diclofenac Drugs 0.000 description 2
- DCOPUUMXTXDBNB-UHFFFAOYSA-N diclofenac Chemical compound OC(=O)CC1=CC=CC=C1NC1=C(Cl)C=CC=C1Cl DCOPUUMXTXDBNB-UHFFFAOYSA-N 0.000 description 2
- AUZONCFQVSMFAP-UHFFFAOYSA-N disulfiram Chemical compound CCN(CC)C(=S)SSC(=S)N(CC)CC AUZONCFQVSMFAP-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- AEUTYOVWOVBAKS-UWVGGRQHSA-N ethambutol Chemical compound CC[C@@H](CO)NCCN[C@@H](CC)CO AEUTYOVWOVBAKS-UWVGGRQHSA-N 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 230000030136 gastric emptying Effects 0.000 description 2
- 238000005469 granulation Methods 0.000 description 2
- 230000003179 granulation Effects 0.000 description 2
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 2
- 230000001939 inductive effect Effects 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000003780 insertion Methods 0.000 description 2
- 230000037431 insertion Effects 0.000 description 2
- 210000000936 intestine Anatomy 0.000 description 2
- 229960002198 irbesartan Drugs 0.000 description 2
- YCPOHTHPUREGFM-UHFFFAOYSA-N irbesartan Chemical compound O=C1N(CC=2C=CC(=CC=2)C=2C(=CC=CC=2)C=2[N]N=NN=2)C(CCCC)=NC21CCCC2 YCPOHTHPUREGFM-UHFFFAOYSA-N 0.000 description 2
- 208000002551 irritable bowel syndrome Diseases 0.000 description 2
- 229960003987 melatonin Drugs 0.000 description 2
- DRLFMBDRBRZALE-UHFFFAOYSA-N melatonin Chemical compound COC1=CC=C2NC=C(CCNC(C)=O)C2=C1 DRLFMBDRBRZALE-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- XQYZDYMELSJDRZ-UHFFFAOYSA-N papaverine Chemical compound C1=C(OC)C(OC)=CC=C1CC1=NC=CC2=CC(OC)=C(OC)C=C12 XQYZDYMELSJDRZ-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229960003330 pentetic acid Drugs 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 230000000069 prophylactic effect Effects 0.000 description 2
- 238000011321 prophylaxis Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000829 suppository Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 229960003991 trazodone Drugs 0.000 description 2
- PHLBKPHSAVXXEF-UHFFFAOYSA-N trazodone Chemical compound ClC1=CC=CC(N2CCN(CCCN3C(N4C=CC=CC4=N3)=O)CC2)=C1 PHLBKPHSAVXXEF-UHFFFAOYSA-N 0.000 description 2
- 230000003442 weekly effect Effects 0.000 description 2
- 238000005303 weighing Methods 0.000 description 2
- IGLYMJRIWWIQQE-QUOODJBBSA-N (1S,2R)-2-phenylcyclopropan-1-amine (1R,2S)-2-phenylcyclopropan-1-amine Chemical compound N[C@H]1C[C@@H]1C1=CC=CC=C1.N[C@@H]1C[C@H]1C1=CC=CC=C1 IGLYMJRIWWIQQE-QUOODJBBSA-N 0.000 description 1
- YKFCISHFRZHKHY-NGQGLHOPSA-N (2s)-2-amino-3-(3,4-dihydroxyphenyl)-2-methylpropanoic acid;trihydrate Chemical compound O.O.O.OC(=O)[C@](N)(C)CC1=CC=C(O)C(O)=C1.OC(=O)[C@](N)(C)CC1=CC=C(O)C(O)=C1 YKFCISHFRZHKHY-NGQGLHOPSA-N 0.000 description 1
- ZGGHKIMDNBDHJB-NRFPMOEYSA-M (3R,5S)-fluvastatin sodium Chemical compound [Na+].C12=CC=CC=C2N(C(C)C)C(\C=C\[C@@H](O)C[C@@H](O)CC([O-])=O)=C1C1=CC=C(F)C=C1 ZGGHKIMDNBDHJB-NRFPMOEYSA-M 0.000 description 1
- MKJIEFSOBYUXJB-HOCLYGCPSA-N (3S,11bS)-9,10-dimethoxy-3-isobutyl-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-a]isoquinolin-2-one Chemical compound C1CN2C[C@H](CC(C)C)C(=O)C[C@H]2C2=C1C=C(OC)C(OC)=C2 MKJIEFSOBYUXJB-HOCLYGCPSA-N 0.000 description 1
- BMPDWHIDQYTSHX-AWEZNQCLSA-N (S)-MHD Chemical compound C1[C@H](O)C2=CC=CC=C2N(C(=O)N)C2=CC=CC=C21 BMPDWHIDQYTSHX-AWEZNQCLSA-N 0.000 description 1
- KWTSXDURSIMDCE-QMMMGPOBSA-N (S)-amphetamine Chemical compound C[C@H](N)CC1=CC=CC=C1 KWTSXDURSIMDCE-QMMMGPOBSA-N 0.000 description 1
- RKUNBYITZUJHSG-FXUDXRNXSA-N (S)-atropine Chemical compound C1([C@@H](CO)C(=O)O[C@H]2C[C@H]3CC[C@@H](C2)N3C)=CC=CC=C1 RKUNBYITZUJHSG-FXUDXRNXSA-N 0.000 description 1
- HNSDLXPSAYFUHK-UHFFFAOYSA-N 1,4-bis(2-ethylhexyl) sulfosuccinate Chemical compound CCCCC(CC)COC(=O)CC(S(O)(=O)=O)C(=O)OCC(CC)CCCC HNSDLXPSAYFUHK-UHFFFAOYSA-N 0.000 description 1
- SVUOLADPCWQTTE-UHFFFAOYSA-N 1h-1,2-benzodiazepine Chemical compound N1N=CC=CC2=CC=CC=C12 SVUOLADPCWQTTE-UHFFFAOYSA-N 0.000 description 1
- GFRUPHOKLBPHTQ-UHFFFAOYSA-N 2-(2-cyclohexyl-2-hydroxy-1-oxo-2-phenylethoxy)ethyl-diethyl-methylammonium Chemical compound C=1C=CC=CC=1C(O)(C(=O)OCC[N+](C)(CC)CC)C1CCCCC1 GFRUPHOKLBPHTQ-UHFFFAOYSA-N 0.000 description 1
- UVKNREAAHQRBKA-IEOVAKBOSA-I 2-[bis[2-[bis(carboxylatomethyl)amino]ethyl]amino]acetate;technetium-99(4+) Chemical compound [99Tc+4].[O-]C(=O)CN(CC([O-])=O)CCN(CC(=O)[O-])CCN(CC([O-])=O)CC([O-])=O UVKNREAAHQRBKA-IEOVAKBOSA-I 0.000 description 1
- JIVPVXMEBJLZRO-CQSZACIVSA-N 2-chloro-5-[(1r)-1-hydroxy-3-oxo-2h-isoindol-1-yl]benzenesulfonamide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC([C@@]2(O)C3=CC=CC=C3C(=O)N2)=C1 JIVPVXMEBJLZRO-CQSZACIVSA-N 0.000 description 1
- JXZZEXZZKAWDSP-UHFFFAOYSA-N 3-(2-(4-Benzamidopiperid-1-yl)ethyl)indole Chemical compound C1CN(CCC=2C3=CC=CC=C3NC=2)CCC1NC(=O)C1=CC=CC=C1 JXZZEXZZKAWDSP-UHFFFAOYSA-N 0.000 description 1
- JVGVDSSUAVXRDY-UHFFFAOYSA-N 3-(4-hydroxyphenyl)lactic acid Chemical compound OC(=O)C(O)CC1=CC=C(O)C=C1 JVGVDSSUAVXRDY-UHFFFAOYSA-N 0.000 description 1
- PMXMIIMHBWHSKN-UHFFFAOYSA-N 3-{2-[4-(6-fluoro-1,2-benzoxazol-3-yl)piperidin-1-yl]ethyl}-9-hydroxy-2-methyl-6,7,8,9-tetrahydropyrido[1,2-a]pyrimidin-4-one Chemical compound FC1=CC=C2C(C3CCN(CC3)CCC=3C(=O)N4CCCC(O)C4=NC=3C)=NOC2=C1 PMXMIIMHBWHSKN-UHFFFAOYSA-N 0.000 description 1
- ZGDLVKWIZHHWIR-UHFFFAOYSA-N 4-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]morpholine Chemical compound O1C(C)(C)C(C)(C)OB1C1=CC=C(N2CCOCC2)N=C1 ZGDLVKWIZHHWIR-UHFFFAOYSA-N 0.000 description 1
- XWSCOGPKWVNQSV-UHFFFAOYSA-N 5-bromo-2,3-dichloropyridine Chemical compound ClC1=CC(Br)=CN=C1Cl XWSCOGPKWVNQSV-UHFFFAOYSA-N 0.000 description 1
- XKFPYPQQHFEXRZ-UHFFFAOYSA-N 5-methyl-N'-(phenylmethyl)-3-isoxazolecarbohydrazide Chemical compound O1C(C)=CC(C(=O)NNCC=2C=CC=CC=2)=N1 XKFPYPQQHFEXRZ-UHFFFAOYSA-N 0.000 description 1
- USSIQXCVUWKGNF-UHFFFAOYSA-N 6-(dimethylamino)-4,4-diphenylheptan-3-one Chemical compound C=1C=CC=CC=1C(CC(C)N(C)C)(C(=O)CC)C1=CC=CC=C1 USSIQXCVUWKGNF-UHFFFAOYSA-N 0.000 description 1
- 229930008281 A03AD01 - Papaverine Natural products 0.000 description 1
- 229930000680 A04AD01 - Scopolamine Natural products 0.000 description 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- CEUORZQYGODEFX-UHFFFAOYSA-N Aripirazole Chemical compound ClC1=CC=CC(N2CCN(CCCCOC=3C=C4NC(=O)CCC4=CC=3)CC2)=C1Cl CEUORZQYGODEFX-UHFFFAOYSA-N 0.000 description 1
- 229930003347 Atropine Natural products 0.000 description 1
- VOVIALXJUBGFJZ-KWVAZRHASA-N Budesonide Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@@H]2[C@@H]1[C@@H]1C[C@H]3OC(CCC)O[C@@]3(C(=O)CO)[C@@]1(C)C[C@@H]2O VOVIALXJUBGFJZ-KWVAZRHASA-N 0.000 description 1
- 239000002083 C09CA01 - Losartan Substances 0.000 description 1
- 239000002080 C09CA02 - Eprosartan Substances 0.000 description 1
- 239000002051 C09CA08 - Olmesartan medoxomil Substances 0.000 description 1
- QAGYKUNXZHXKMR-UHFFFAOYSA-N CPD000469186 Natural products CC1=C(O)C=CC=C1C(=O)NC(C(O)CN1C(CC2CCCCC2C1)C(=O)NC(C)(C)C)CSC1=CC=CC=C1 QAGYKUNXZHXKMR-UHFFFAOYSA-N 0.000 description 1
- GHOSNRCGJFBJIB-UHFFFAOYSA-N Candesartan cilexetil Chemical compound C=12N(CC=3C=CC(=CC=3)C=3C(=CC=CC=3)C3=NNN=N3)C(OCC)=NC2=CC=CC=1C(=O)OC(C)OC(=O)OC1CCCCC1 GHOSNRCGJFBJIB-UHFFFAOYSA-N 0.000 description 1
- JOATXPAWOHTVSZ-UHFFFAOYSA-N Celiprolol Chemical compound CCN(CC)C(=O)NC1=CC=C(OCC(O)CNC(C)(C)C)C(C(C)=O)=C1 JOATXPAWOHTVSZ-UHFFFAOYSA-N 0.000 description 1
- 208000035484 Cellulite Diseases 0.000 description 1
- GDLIGKIOYRNHDA-UHFFFAOYSA-N Clomipramine Chemical compound C1CC2=CC=C(Cl)C=C2N(CCCN(C)C)C2=CC=CC=C21 GDLIGKIOYRNHDA-UHFFFAOYSA-N 0.000 description 1
- 241000223205 Coccidioides immitis Species 0.000 description 1
- 208000010007 Cogan syndrome Diseases 0.000 description 1
- DYDCUQKUCUHJBH-UWTATZPHSA-N D-Cycloserine Chemical compound N[C@@H]1CONC1=O DYDCUQKUCUHJBH-UWTATZPHSA-N 0.000 description 1
- DYDCUQKUCUHJBH-UHFFFAOYSA-N D-Cycloserine Natural products NC1CONC1=O DYDCUQKUCUHJBH-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 description 1
- 208000016192 Demyelinating disease Diseases 0.000 description 1
- LMHIPJMTZHDKEW-XQYLJSSYSA-M Epoprostenol sodium Chemical compound [Na+].O1\C(=C/CCCC([O-])=O)C[C@@H]2[C@@H](/C=C/[C@@H](O)CCCCC)[C@H](O)C[C@@H]21 LMHIPJMTZHDKEW-XQYLJSSYSA-M 0.000 description 1
- KGWDUNBJIMUFAP-KVVVOXFISA-N Ethanolamine Oleate Chemical compound NCCO.CCCCCCCC\C=C/CCCCCCCC(O)=O KGWDUNBJIMUFAP-KVVVOXFISA-N 0.000 description 1
- PLDUPXSUYLZYBN-UHFFFAOYSA-N Fluphenazine Chemical compound C1CN(CCO)CCN1CCCN1C2=CC(C(F)(F)F)=CC=C2SC2=CC=CC=C21 PLDUPXSUYLZYBN-UHFFFAOYSA-N 0.000 description 1
- 229930091371 Fructose Natural products 0.000 description 1
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
- 239000005715 Fructose Substances 0.000 description 1
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 1
- 208000018522 Gastrointestinal disease Diseases 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 208000003807 Graves Disease Diseases 0.000 description 1
- 208000001204 Hashimoto Disease Diseases 0.000 description 1
- 208000032843 Hemorrhage Diseases 0.000 description 1
- 229930010555 Inosine Natural products 0.000 description 1
- UGQMRVRMYYASKQ-KQYNXXCUSA-N Inosine Chemical compound O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C2=NC=NC(O)=C2N=C1 UGQMRVRMYYASKQ-KQYNXXCUSA-N 0.000 description 1
- 102000003996 Interferon-beta Human genes 0.000 description 1
- 108090000467 Interferon-beta Proteins 0.000 description 1
- JUZNIMUFDBIJCM-ANEDZVCMSA-N Invanz Chemical compound O=C([C@H]1NC[C@H](C1)SC=1[C@H](C)[C@@H]2[C@H](C(N2C=1C(O)=O)=O)[C@H](O)C)NC1=CC=CC(C(O)=O)=C1 JUZNIMUFDBIJCM-ANEDZVCMSA-N 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- 240000008415 Lactuca sativa Species 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 240000005856 Lyophyllum decastes Species 0.000 description 1
- 235000013194 Lyophyllum decastes Nutrition 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- JRRNZNSGDSFFIR-UHFFFAOYSA-M Mepenzolate bromide Chemical compound [Br-].C1[N+](C)(C)CCCC1OC(=O)C(O)(C=1C=CC=CC=1)C1=CC=CC=C1 JRRNZNSGDSFFIR-UHFFFAOYSA-M 0.000 description 1
- XADCESSVHJOZHK-UHFFFAOYSA-N Meperidine Chemical compound C=1C=CC=CC=1C1(C(=O)OCC)CCN(C)CC1 XADCESSVHJOZHK-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- FQISKWAFAHGMGT-SGJOWKDISA-M Methylprednisolone sodium succinate Chemical compound [Na+].C([C@@]12C)=CC(=O)C=C1[C@@H](C)C[C@@H]1[C@@H]2[C@@H](O)C[C@]2(C)[C@@](O)(C(=O)COC(=O)CCC([O-])=O)CC[C@H]21 FQISKWAFAHGMGT-SGJOWKDISA-M 0.000 description 1
- UEQUQVLFIPOEMF-UHFFFAOYSA-N Mianserin Chemical compound C1C2=CC=CC=C2N2CCN(C)CC2C2=CC=CC=C21 UEQUQVLFIPOEMF-UHFFFAOYSA-N 0.000 description 1
- WPNJAUFVNXKLIM-UHFFFAOYSA-N Moxonidine Chemical compound COC1=NC(C)=NC(Cl)=C1NC1=NCCN1 WPNJAUFVNXKLIM-UHFFFAOYSA-N 0.000 description 1
- XKLMZUWKNUAPSZ-UHFFFAOYSA-N N-(2,6-dimethylphenyl)-2-{4-[2-hydroxy-3-(2-methoxyphenoxy)propyl]piperazin-1-yl}acetamide Chemical compound COC1=CC=CC=C1OCC(O)CN1CCN(CC(=O)NC=2C(=CC=CC=2C)C)CC1 XKLMZUWKNUAPSZ-UHFFFAOYSA-N 0.000 description 1
- YLXDSYKOBKBWJQ-LBPRGKRZSA-N N-[2-[(8S)-2,6,7,8-tetrahydro-1H-cyclopenta[e]benzofuran-8-yl]ethyl]propanamide Chemical compound C1=C2OCCC2=C2[C@H](CCNC(=O)CC)CCC2=C1 YLXDSYKOBKBWJQ-LBPRGKRZSA-N 0.000 description 1
- CMWTZPSULFXXJA-UHFFFAOYSA-N Naproxen Natural products C1=C(C(C)C(O)=O)C=CC2=CC(OC)=CC=C21 CMWTZPSULFXXJA-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- UQGKUQLKSCSZGY-UHFFFAOYSA-N Olmesartan medoxomil Chemical compound C=1C=C(C=2C(=CC=CC=2)C2=NNN=N2)C=CC=1CN1C(CCC)=NC(C(C)(C)O)=C1C(=O)OCC=1OC(=O)OC=1C UQGKUQLKSCSZGY-UHFFFAOYSA-N 0.000 description 1
- 229940123257 Opioid receptor antagonist Drugs 0.000 description 1
- BRUQQQPBMZOVGD-XFKAJCMBSA-N Oxycodone Chemical compound O=C([C@@H]1O2)CC[C@@]3(O)[C@H]4CC5=CC=C(OC)C2=C5[C@@]13CCN4C BRUQQQPBMZOVGD-XFKAJCMBSA-N 0.000 description 1
- DUDKAZCAISNGQN-UHFFFAOYSA-N Oxyphencyclimine Chemical compound CN1CCCN=C1COC(=O)C(O)(C=1C=CC=CC=1)C1CCCCC1 DUDKAZCAISNGQN-UHFFFAOYSA-N 0.000 description 1
- IQPSEEYGBUAQFF-UHFFFAOYSA-N Pantoprazole Chemical compound COC1=CC=NC(CS(=O)C=2NC3=CC=C(OC(F)F)C=C3N=2)=C1OC IQPSEEYGBUAQFF-UHFFFAOYSA-N 0.000 description 1
- 206010049752 Peau d'orange Diseases 0.000 description 1
- RMUCZJUITONUFY-UHFFFAOYSA-N Phenelzine Chemical compound NNCCC1=CC=CC=C1 RMUCZJUITONUFY-UHFFFAOYSA-N 0.000 description 1
- 206010037660 Pyrexia Diseases 0.000 description 1
- 208000033464 Reiter syndrome Diseases 0.000 description 1
- IWUCXVSUMQZMFG-AFCXAGJDSA-N Ribavirin Chemical compound N1=C(C(=O)N)N=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O1 IWUCXVSUMQZMFG-AFCXAGJDSA-N 0.000 description 1
- NCDNCNXCDXHOMX-UHFFFAOYSA-N Ritonavir Natural products C=1C=CC=CC=1CC(NC(=O)OCC=1SC=NC=1)C(O)CC(CC=1C=CC=CC=1)NC(=O)C(C(C)C)NC(=O)N(C)CC1=CSC(C(C)C)=N1 NCDNCNXCDXHOMX-UHFFFAOYSA-N 0.000 description 1
- 206010039705 Scleritis Diseases 0.000 description 1
- 208000021386 Sjogren Syndrome Diseases 0.000 description 1
- 206010041349 Somnolence Diseases 0.000 description 1
- 208000007107 Stomach Ulcer Diseases 0.000 description 1
- 108010023197 Streptokinase Proteins 0.000 description 1
- GKLVYJBZJHMRIY-OUBTZVSYSA-N Technetium-99 Chemical compound [99Tc] GKLVYJBZJHMRIY-OUBTZVSYSA-N 0.000 description 1
- 108010039185 Tenecteplase Proteins 0.000 description 1
- 244000299461 Theobroma cacao Species 0.000 description 1
- 235000009470 Theobroma cacao Nutrition 0.000 description 1
- 206010064996 Ulcerative keratitis Diseases 0.000 description 1
- 108090000435 Urokinase-type plasminogen activator Proteins 0.000 description 1
- 102000003990 Urokinase-type plasminogen activator Human genes 0.000 description 1
- 244000126014 Valeriana officinalis Species 0.000 description 1
- 235000013832 Valeriana officinalis Nutrition 0.000 description 1
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 description 1
- ANGKOCUUWGHLCE-HKUYNNGSSA-N [(3s)-1,1-dimethylpyrrolidin-1-ium-3-yl] (2r)-2-cyclopentyl-2-hydroxy-2-phenylacetate Chemical compound C1[N+](C)(C)CC[C@@H]1OC(=O)[C@](O)(C=1C=CC=CC=1)C1CCCC1 ANGKOCUUWGHLCE-HKUYNNGSSA-N 0.000 description 1
- ZWBTYMGEBZUQTK-PVLSIAFMSA-N [(7S,9E,11S,12R,13S,14R,15R,16R,17S,18S,19E,21Z)-2,15,17,32-tetrahydroxy-11-methoxy-3,7,12,14,16,18,22-heptamethyl-1'-(2-methylpropyl)-6,23-dioxospiro[8,33-dioxa-24,27,29-triazapentacyclo[23.6.1.14,7.05,31.026,30]tritriaconta-1(32),2,4,9,19,21,24,26,30-nonaene-28,4'-piperidine]-13-yl] acetate Chemical compound CO[C@H]1\C=C\O[C@@]2(C)Oc3c(C2=O)c2c4NC5(CCN(CC(C)C)CC5)N=c4c(=NC(=O)\C(C)=C/C=C/[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C)c(O)c2c(O)c3C ZWBTYMGEBZUQTK-PVLSIAFMSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- AFCGFAGUEYAMAO-UHFFFAOYSA-N acamprosate Chemical compound CC(=O)NCCCS(O)(=O)=O AFCGFAGUEYAMAO-UHFFFAOYSA-N 0.000 description 1
- 229960004047 acamprosate Drugs 0.000 description 1
- 229960002122 acebutolol Drugs 0.000 description 1
- GOEMGAFJFRBGGG-UHFFFAOYSA-N acebutolol Chemical compound CCCC(=O)NC1=CC=C(OCC(O)CNC(C)C)C(C(C)=O)=C1 GOEMGAFJFRBGGG-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 229960002964 adalimumab Drugs 0.000 description 1
- 229960003205 adefovir dipivoxil Drugs 0.000 description 1
- FLZQKRKHLSUHOR-UHFFFAOYSA-N alosetron Chemical compound CC1=NC=N[C]1CN1C(=O)C(C=2C(=CC=CC=2)N2C)=C2CC1 FLZQKRKHLSUHOR-UHFFFAOYSA-N 0.000 description 1
- 229960003550 alosetron Drugs 0.000 description 1
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 description 1
- 229960003318 alteplase Drugs 0.000 description 1
- 229940024545 aluminum hydroxide Drugs 0.000 description 1
- 239000002269 analeptic agent Substances 0.000 description 1
- 230000000202 analgesic effect Effects 0.000 description 1
- 229940035676 analgesics Drugs 0.000 description 1
- 229940035674 anesthetics Drugs 0.000 description 1
- 239000000730 antalgic agent Substances 0.000 description 1
- 230000003257 anti-anginal effect Effects 0.000 description 1
- 230000002924 anti-infective effect Effects 0.000 description 1
- 230000000118 anti-neoplastic effect Effects 0.000 description 1
- 229940125681 anticonvulsant agent Drugs 0.000 description 1
- 239000001961 anticonvulsive agent Substances 0.000 description 1
- 239000003472 antidiabetic agent Substances 0.000 description 1
- 229940125708 antidiabetic agent Drugs 0.000 description 1
- 229940125715 antihistaminic agent Drugs 0.000 description 1
- 239000000739 antihistaminic agent Substances 0.000 description 1
- 229960005475 antiinfective agent Drugs 0.000 description 1
- 229940034982 antineoplastic agent Drugs 0.000 description 1
- 239000002246 antineoplastic agent Substances 0.000 description 1
- 239000000939 antiparkinson agent Substances 0.000 description 1
- 239000003435 antirheumatic agent Substances 0.000 description 1
- 239000002830 appetite depressant Substances 0.000 description 1
- 239000002948 appetite stimulant Substances 0.000 description 1
- 229940029995 appetite stimulants Drugs 0.000 description 1
- 229960004372 aripiprazole Drugs 0.000 description 1
- 229960000981 artemether Drugs 0.000 description 1
- 229960000396 atropine Drugs 0.000 description 1
- RKUNBYITZUJHSG-SPUOUPEWSA-N atropine Chemical compound O([C@H]1C[C@H]2CC[C@@H](C1)N2C)C(=O)C(CO)C1=CC=CC=C1 RKUNBYITZUJHSG-SPUOUPEWSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 229940116224 behenate Drugs 0.000 description 1
- UKMSUNONTOPOIO-UHFFFAOYSA-M behenate Chemical compound CCCCCCCCCCCCCCCCCCCCCC([O-])=O UKMSUNONTOPOIO-UHFFFAOYSA-M 0.000 description 1
- 229960003616 bemiparin Drugs 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 150000001557 benzodiazepines Chemical class 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- IQFYYKKMVGJFEH-UHFFFAOYSA-N beta-L-thymidine Natural products O=C1NC(=O)C(C)=CN1C1OC(CO)C(O)C1 IQFYYKKMVGJFEH-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- YSXKPIUOCJLQIE-UHFFFAOYSA-N biperiden Chemical compound C1C(C=C2)CC2C1C(C=1C=CC=CC=1)(O)CCN1CCCCC1 YSXKPIUOCJLQIE-UHFFFAOYSA-N 0.000 description 1
- 229960003003 biperiden Drugs 0.000 description 1
- 229960000503 bisacodyl Drugs 0.000 description 1
- 229960002781 bisoprolol Drugs 0.000 description 1
- VHYCDWMUTMEGQY-UHFFFAOYSA-N bisoprolol Chemical compound CC(C)NCC(O)COC1=CC=C(COCCOC(C)C)C=C1 VHYCDWMUTMEGQY-UHFFFAOYSA-N 0.000 description 1
- 208000034158 bleeding Diseases 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 230000004097 bone metabolism Effects 0.000 description 1
- 235000021152 breakfast Nutrition 0.000 description 1
- 229960002802 bromocriptine Drugs 0.000 description 1
- OZVBMTJYIDMWIL-AYFBDAFISA-N bromocriptine Chemical compound C1=CC(C=2[C@H](N(C)C[C@@H](C=2)C(=O)N[C@]2(C(=O)N3[C@H](C(N4CCC[C@H]4[C@]3(O)O2)=O)CC(C)C)C(C)C)C2)=C3C2=C(Br)NC3=C1 OZVBMTJYIDMWIL-AYFBDAFISA-N 0.000 description 1
- 201000009267 bronchiectasis Diseases 0.000 description 1
- 229960004436 budesonide Drugs 0.000 description 1
- 229960001058 bupropion Drugs 0.000 description 1
- SNPPWIUOZRMYNY-UHFFFAOYSA-N bupropion Chemical compound CC(C)(C)NC(C)C(=O)C1=CC=CC(Cl)=C1 SNPPWIUOZRMYNY-UHFFFAOYSA-N 0.000 description 1
- 229960001113 butorphanol Drugs 0.000 description 1
- YBCNXCRZPWQOBR-WVHCHWADSA-N butylscopolamine Chemical compound C1([C@@H](CO)C(=O)O[C@H]2C[C@@H]3[N+]([C@H](C2)[C@@H]2[C@H]3O2)(C)CCCC)=CC=CC=C1 YBCNXCRZPWQOBR-WVHCHWADSA-N 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 229960004349 candesartan cilexetil Drugs 0.000 description 1
- 239000007963 capsule composition Substances 0.000 description 1
- 239000002327 cardiovascular agent Substances 0.000 description 1
- 229940125692 cardiovascular agent Drugs 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 229960004195 carvedilol Drugs 0.000 description 1
- NPAKNKYSJIDKMW-UHFFFAOYSA-N carvedilol Chemical compound COC1=CC=CC=C1OCCNCC(O)COC1=CC=CC2=NC3=CC=C[CH]C3=C12 NPAKNKYSJIDKMW-UHFFFAOYSA-N 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 229960002129 cefixime Drugs 0.000 description 1
- OKBVVJOGVLARMR-QSWIMTSFSA-N cefixime Chemical compound S1C(N)=NC(C(=N\OCC(O)=O)\C(=O)N[C@@H]2C(N3C(=C(C=C)CS[C@@H]32)C(O)=O)=O)=C1 OKBVVJOGVLARMR-QSWIMTSFSA-N 0.000 description 1
- 229960004261 cefotaxime Drugs 0.000 description 1
- AZZMGZXNTDTSME-JUZDKLSSSA-M cefotaxime sodium Chemical compound [Na+].N([C@@H]1C(N2C(=C(COC(C)=O)CS[C@@H]21)C([O-])=O)=O)C(=O)\C(=N/OC)C1=CSC(N)=N1 AZZMGZXNTDTSME-JUZDKLSSSA-M 0.000 description 1
- 229960002588 cefradine Drugs 0.000 description 1
- 229960000484 ceftazidime Drugs 0.000 description 1
- NMVPEQXCMGEDNH-TZVUEUGBSA-N ceftazidime pentahydrate Chemical compound O.O.O.O.O.S([C@@H]1[C@@H](C(N1C=1C([O-])=O)=O)NC(=O)\C(=N/OC(C)(C)C(O)=O)C=2N=C(N)SC=2)CC=1C[N+]1=CC=CC=C1 NMVPEQXCMGEDNH-TZVUEUGBSA-N 0.000 description 1
- 229960001668 cefuroxime Drugs 0.000 description 1
- JFPVXVDWJQMJEE-IZRZKJBUSA-N cefuroxime Chemical compound N([C@@H]1C(N2C(=C(COC(N)=O)CS[C@@H]21)C(O)=O)=O)C(=O)\C(=N/OC)C1=CC=CO1 JFPVXVDWJQMJEE-IZRZKJBUSA-N 0.000 description 1
- RZEKVGVHFLEQIL-UHFFFAOYSA-N celecoxib Chemical compound C1=CC(C)=CC=C1C1=CC(C(F)(F)F)=NN1C1=CC=C(S(N)(=O)=O)C=C1 RZEKVGVHFLEQIL-UHFFFAOYSA-N 0.000 description 1
- 229960000590 celecoxib Drugs 0.000 description 1
- 229960002320 celiprolol Drugs 0.000 description 1
- 230000036232 cellulite Effects 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 239000003874 central nervous system depressant Substances 0.000 description 1
- 229940083181 centrally acting adntiadrenergic agent methyldopa Drugs 0.000 description 1
- 229940106164 cephalexin Drugs 0.000 description 1
- ZAIPMKNFIOOWCQ-UEKVPHQBSA-N cephalexin Chemical compound C1([C@@H](N)C(=O)N[C@H]2[C@@H]3N(C2=O)C(=C(CS3)C)C(O)=O)=CC=CC=C1 ZAIPMKNFIOOWCQ-UEKVPHQBSA-N 0.000 description 1
- RDLPVSKMFDYCOR-UEKVPHQBSA-N cephradine Chemical compound C1([C@@H](N)C(=O)N[C@H]2[C@@H]3N(C2=O)C(=C(CS3)C)C(O)=O)=CCC=CC1 RDLPVSKMFDYCOR-UEKVPHQBSA-N 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 229960001523 chlortalidone Drugs 0.000 description 1
- 201000001883 cholelithiasis Diseases 0.000 description 1
- QBPFLULOKWLNNW-UHFFFAOYSA-N chrysazin Chemical compound O=C1C2=CC=CC(O)=C2C(=O)C2=C1C=CC=C2O QBPFLULOKWLNNW-UHFFFAOYSA-N 0.000 description 1
- 229960001380 cimetidine Drugs 0.000 description 1
- 230000027288 circadian rhythm Effects 0.000 description 1
- 229960004606 clomipramine Drugs 0.000 description 1
- 201000003486 coccidioidomycosis Diseases 0.000 description 1
- 235000016213 coffee Nutrition 0.000 description 1
- 235000013353 coffee beverage Nutrition 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 210000001072 colon Anatomy 0.000 description 1
- 239000007891 compressed tablet Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000008358 core component Substances 0.000 description 1
- 201000007717 corneal ulcer Diseases 0.000 description 1
- 229960003077 cycloserine Drugs 0.000 description 1
- 229960004969 dalteparin Drugs 0.000 description 1
- 229960001577 dantron Drugs 0.000 description 1
- 229960005107 darunavir Drugs 0.000 description 1
- CJBJHOAVZSMMDJ-HEXNFIEUSA-N darunavir Chemical compound C([C@@H]([C@H](O)CN(CC(C)C)S(=O)(=O)C=1C=CC(N)=CC=1)NC(=O)O[C@@H]1[C@@H]2CCO[C@@H]2OC1)C1=CC=CC=C1 CJBJHOAVZSMMDJ-HEXNFIEUSA-N 0.000 description 1
- 239000000850 decongestant Substances 0.000 description 1
- 229940124581 decongestants Drugs 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 229960004193 dextropropoxyphene Drugs 0.000 description 1
- XLMALTXPSGQGBX-GCJKJVERSA-N dextropropoxyphene Chemical compound C([C@](OC(=O)CC)([C@H](C)CN(C)C)C=1C=CC=CC=1)C1=CC=CC=C1 XLMALTXPSGQGBX-GCJKJVERSA-N 0.000 description 1
- CURUTKGFNZGFSE-UHFFFAOYSA-N dicyclomine Chemical compound C1CCCCC1C1(C(=O)OCCN(CC)CC)CCCCC1 CURUTKGFNZGFSE-UHFFFAOYSA-N 0.000 description 1
- 229960002777 dicycloverine Drugs 0.000 description 1
- SSAJNPNVUYMUCI-UHFFFAOYSA-N diethyl-[2-[2-(naphthalen-1-ylmethyl)-3-(oxolan-2-yl)propanoyl]oxyethyl]azanium;2-hydroxy-2-oxoacetate Chemical compound OC(=O)C([O-])=O.C=1C=CC2=CC=CC=C2C=1CC(C(=O)OCC[NH+](CC)CC)CC1CCCO1 SSAJNPNVUYMUCI-UHFFFAOYSA-N 0.000 description 1
- 230000001079 digestive effect Effects 0.000 description 1
- XYYVYLMBEZUESM-UHFFFAOYSA-N dihydrocodeine Natural products C1C(N(CCC234)C)C2C=CC(=O)C3OC2=C4C1=CC=C2OC XYYVYLMBEZUESM-UHFFFAOYSA-N 0.000 description 1
- AMTWCFIAVKBGOD-UHFFFAOYSA-N dioxosilane;methoxy-dimethyl-trimethylsilyloxysilane Chemical compound O=[Si]=O.CO[Si](C)(C)O[Si](C)(C)C AMTWCFIAVKBGOD-UHFFFAOYSA-N 0.000 description 1
- 229960000520 diphenhydramine Drugs 0.000 description 1
- XEYBHCRIKKKOSS-UHFFFAOYSA-N disodium;azanylidyneoxidanium;iron(2+);pentacyanide Chemical compound [Na+].[Na+].[Fe+2].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].[O+]#N XEYBHCRIKKKOSS-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 229960002563 disulfiram Drugs 0.000 description 1
- 229940018602 docusate Drugs 0.000 description 1
- 239000003136 dopamine receptor stimulating agent Substances 0.000 description 1
- 229960001389 doxazosin Drugs 0.000 description 1
- RUZYUOTYCVRMRZ-UHFFFAOYSA-N doxazosin Chemical compound C1OC2=CC=CC=C2OC1C(=O)N(CC1)CCN1C1=NC(N)=C(C=C(C(OC)=C2)OC)C2=N1 RUZYUOTYCVRMRZ-UHFFFAOYSA-N 0.000 description 1
- 229960005426 doxepin Drugs 0.000 description 1
- ODQWQRRAPPTVAG-GZTJUZNOSA-N doxepin Chemical compound C1OC2=CC=CC=C2C(=C/CCN(C)C)/C2=CC=CC=C21 ODQWQRRAPPTVAG-GZTJUZNOSA-N 0.000 description 1
- 229960002065 drotaverine Drugs 0.000 description 1
- OMFNSKIUKYOYRG-MOSHPQCFSA-N drotaverine Chemical compound C1=C(OCC)C(OCC)=CC=C1\C=C/1C2=CC(OCC)=C(OCC)C=C2CCN\1 OMFNSKIUKYOYRG-MOSHPQCFSA-N 0.000 description 1
- 238000012377 drug delivery Methods 0.000 description 1
- 208000000718 duodenal ulcer Diseases 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 229940037395 electrolytes Drugs 0.000 description 1
- 229960000980 entecavir Drugs 0.000 description 1
- YXPVEXCTPGULBZ-WQYNNSOESA-N entecavir hydrate Chemical compound O.C1=NC=2C(=O)NC(N)=NC=2N1[C@H]1C[C@H](O)[C@@H](CO)C1=C YXPVEXCTPGULBZ-WQYNNSOESA-N 0.000 description 1
- 229960004563 eprosartan Drugs 0.000 description 1
- OROAFUQRIXKEMV-LDADJPATSA-N eprosartan Chemical compound C=1C=C(C(O)=O)C=CC=1CN1C(CCCC)=NC=C1\C=C(C(O)=O)/CC1=CC=CS1 OROAFUQRIXKEMV-LDADJPATSA-N 0.000 description 1
- 229960002770 ertapenem Drugs 0.000 description 1
- 229960004028 eslicarbazepine Drugs 0.000 description 1
- 229960003745 esmolol Drugs 0.000 description 1
- AQNDDEOPVVGCPG-UHFFFAOYSA-N esmolol Chemical compound COC(=O)CCC1=CC=C(OCC(O)CNC(C)C)C=C1 AQNDDEOPVVGCPG-UHFFFAOYSA-N 0.000 description 1
- 229960004770 esomeprazole Drugs 0.000 description 1
- SUBDBMMJDZJVOS-DEOSSOPVSA-N esomeprazole Chemical compound C([S@](=O)C1=NC2=CC=C(C=C2N1)OC)C1=NC=C(C)C(OC)=C1C SUBDBMMJDZJVOS-DEOSSOPVSA-N 0.000 description 1
- 229960000285 ethambutol Drugs 0.000 description 1
- 229940031124 ethanolamine oleate Drugs 0.000 description 1
- 229960002767 ethosuximide Drugs 0.000 description 1
- HAPOVYFOVVWLRS-UHFFFAOYSA-N ethosuximide Chemical compound CCC1(C)CC(=O)NC1=O HAPOVYFOVVWLRS-UHFFFAOYSA-N 0.000 description 1
- 229960005293 etodolac Drugs 0.000 description 1
- XFBVBWWRPKNWHW-UHFFFAOYSA-N etodolac Chemical compound C1COC(CC)(CC(O)=O)C2=N[C]3C(CC)=CC=CC3=C21 XFBVBWWRPKNWHW-UHFFFAOYSA-N 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- XRECTZIEBJDKEO-UHFFFAOYSA-N flucytosine Chemical compound NC1=NC(=O)NC=C1F XRECTZIEBJDKEO-UHFFFAOYSA-N 0.000 description 1
- 229960004413 flucytosine Drugs 0.000 description 1
- 229960002690 fluphenazine Drugs 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 229960003142 fosamprenavir Drugs 0.000 description 1
- MLBVMOWEQCZNCC-OEMFJLHTSA-N fosamprenavir Chemical compound C([C@@H]([C@H](OP(O)(O)=O)CN(CC(C)C)S(=O)(=O)C=1C=CC(N)=CC=1)NC(=O)O[C@@H]1COCC1)C1=CC=CC=C1 MLBVMOWEQCZNCC-OEMFJLHTSA-N 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 229940050411 fumarate Drugs 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 229960002870 gabapentin Drugs 0.000 description 1
- 229930182830 galactose Natural products 0.000 description 1
- 208000001130 gallstones Diseases 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 210000004051 gastric juice Anatomy 0.000 description 1
- 239000004083 gastrointestinal agent Substances 0.000 description 1
- 229940125695 gastrointestinal agent Drugs 0.000 description 1
- SDUQYLNIPVEERB-QPPQHZFASA-N gemcitabine Chemical compound O=C1N=C(N)C=CN1[C@H]1C(F)(F)[C@H](O)[C@@H](CO)O1 SDUQYLNIPVEERB-QPPQHZFASA-N 0.000 description 1
- 229960005277 gemcitabine Drugs 0.000 description 1
- 239000003193 general anesthetic agent Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 1
- 229940049654 glyceryl behenate Drugs 0.000 description 1
- 125000003976 glyceryl group Chemical group [H]C([*])([H])C(O[H])([H])C(O[H])([H])[H] 0.000 description 1
- 229960002462 glycopyrronium bromide Drugs 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229960002096 guanethidine monosulfate Drugs 0.000 description 1
- YUFWAVFNITUSHI-UHFFFAOYSA-N guanethidine monosulfate Chemical compound [H+].[H+].[O-]S([O-])(=O)=O.NC(=N)NCCN1CCCCCCC1 YUFWAVFNITUSHI-UHFFFAOYSA-N 0.000 description 1
- 208000019622 heart disease Diseases 0.000 description 1
- 235000015092 herbal tea Nutrition 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 229940077716 histamine h2 receptor antagonists for peptic ulcer and gord Drugs 0.000 description 1
- LLPOLZWFYMWNKH-CMKMFDCUSA-N hydrocodone Chemical compound C([C@H]1[C@H](N(CC[C@@]112)C)C3)CC(=O)[C@@H]1OC1=C2C3=CC=C1OC LLPOLZWFYMWNKH-CMKMFDCUSA-N 0.000 description 1
- 229960000240 hydrocodone Drugs 0.000 description 1
- WVLOADHCBXTIJK-YNHQPCIGSA-N hydromorphone Chemical compound O([C@H]1C(CC[C@H]23)=O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O WVLOADHCBXTIJK-YNHQPCIGSA-N 0.000 description 1
- 229960001410 hydromorphone Drugs 0.000 description 1
- 229930005342 hyoscyamine Natural products 0.000 description 1
- 229960003210 hyoscyamine Drugs 0.000 description 1
- 210000003405 ileum Anatomy 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 239000012729 immediate-release (IR) formulation Substances 0.000 description 1
- 239000002955 immunomodulating agent Substances 0.000 description 1
- 229940121354 immunomodulator Drugs 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 229960001936 indinavir Drugs 0.000 description 1
- CBVCZFGXHXORBI-PXQQMZJSSA-N indinavir Chemical compound C([C@H](N(CC1)C[C@@H](O)C[C@@H](CC=2C=CC=CC=2)C(=O)N[C@H]2C3=CC=CC=C3C[C@H]2O)C(=O)NC(C)(C)C)N1CC1=CC=CN=C1 CBVCZFGXHXORBI-PXQQMZJSSA-N 0.000 description 1
- 229960002056 indoramin Drugs 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 229960000598 infliximab Drugs 0.000 description 1
- 229960003786 inosine Drugs 0.000 description 1
- 229960001388 interferon-beta Drugs 0.000 description 1
- 229960002672 isocarboxazid Drugs 0.000 description 1
- 229960003350 isoniazid Drugs 0.000 description 1
- QRXWMOHMRWLFEY-UHFFFAOYSA-N isoniazide Chemical compound NNC(=O)C1=CC=NC=C1 QRXWMOHMRWLFEY-UHFFFAOYSA-N 0.000 description 1
- 206010023332 keratitis Diseases 0.000 description 1
- 229960002623 lacosamide Drugs 0.000 description 1
- VPPJLAIAVCUEMN-GFCCVEGCSA-N lacosamide Chemical compound COC[C@@H](NC(C)=O)C(=O)NCC1=CC=CC=C1 VPPJLAIAVCUEMN-GFCCVEGCSA-N 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 229960001848 lamotrigine Drugs 0.000 description 1
- PYZRQGJRPPTADH-UHFFFAOYSA-N lamotrigine Chemical compound NC1=NC(N)=NN=C1C1=CC=CC(Cl)=C1Cl PYZRQGJRPPTADH-UHFFFAOYSA-N 0.000 description 1
- GGXICVAJURFBLW-CEYXHVGTSA-N latanoprost Chemical compound CC(C)OC(=O)CCC\C=C/C[C@H]1[C@@H](O)C[C@@H](O)[C@@H]1CC[C@@H](O)CCC1=CC=CC=C1 GGXICVAJURFBLW-CEYXHVGTSA-N 0.000 description 1
- 229960001160 latanoprost Drugs 0.000 description 1
- 229960004002 levetiracetam Drugs 0.000 description 1
- HPHUVLMMVZITSG-ZCFIWIBFSA-N levetiracetam Chemical compound CC[C@H](C(N)=O)N1CCCC1=O HPHUVLMMVZITSG-ZCFIWIBFSA-N 0.000 description 1
- 229960003406 levorphanol Drugs 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229960002813 lofepramine Drugs 0.000 description 1
- SAPNXPWPAUFAJU-UHFFFAOYSA-N lofepramine Chemical compound C12=CC=CC=C2CCC2=CC=CC=C2N1CCCN(C)CC(=O)C1=CC=C(Cl)C=C1 SAPNXPWPAUFAJU-UHFFFAOYSA-N 0.000 description 1
- 229960004773 losartan Drugs 0.000 description 1
- KJJZZJSZUJXYEA-UHFFFAOYSA-N losartan Chemical compound CCCCC1=NC(Cl)=C(CO)N1CC1=CC=C(C=2C(=CC=CC=2)C=2[N]N=NN=2)C=C1 KJJZZJSZUJXYEA-UHFFFAOYSA-N 0.000 description 1
- 235000004213 low-fat Nutrition 0.000 description 1
- 229960001708 magnesium carbonate Drugs 0.000 description 1
- 230000007257 malfunction Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 1
- 229960001797 methadone Drugs 0.000 description 1
- LZCOQTDXKCNBEE-IKIFYQGPSA-N methscopolamine Chemical compound C1([C@@H](CO)C(=O)O[C@H]2C[C@@H]3[N+]([C@H](C2)[C@@H]2[C@H]3O2)(C)C)=CC=CC=C1 LZCOQTDXKCNBEE-IKIFYQGPSA-N 0.000 description 1
- 229960001383 methylscopolamine Drugs 0.000 description 1
- 229960002817 metolazone Drugs 0.000 description 1
- AQCHWTWZEMGIFD-UHFFFAOYSA-N metolazone Chemical compound CC1NC2=CC(Cl)=C(S(N)(=O)=O)C=C2C(=O)N1C1=CC=CC=C1C AQCHWTWZEMGIFD-UHFFFAOYSA-N 0.000 description 1
- 229960003955 mianserin Drugs 0.000 description 1
- 239000011812 mixed powder Substances 0.000 description 1
- YHXISWVBGDMDLQ-UHFFFAOYSA-N moclobemide Chemical compound C1=CC(Cl)=CC=C1C(=O)NCCN1CCOCC1 YHXISWVBGDMDLQ-UHFFFAOYSA-N 0.000 description 1
- 229960004644 moclobemide Drugs 0.000 description 1
- 229910000402 monopotassium phosphate Inorganic materials 0.000 description 1
- 235000019796 monopotassium phosphate Nutrition 0.000 description 1
- 229960002902 moxaverine Drugs 0.000 description 1
- MYCMTMIGRXJNSO-UHFFFAOYSA-N moxaverine Chemical compound N=1C(CC)=CC2=CC(OC)=C(OC)C=C2C=1CC1=CC=CC=C1 MYCMTMIGRXJNSO-UHFFFAOYSA-N 0.000 description 1
- 229960003938 moxonidine Drugs 0.000 description 1
- 229940035363 muscle relaxants Drugs 0.000 description 1
- 239000003158 myorelaxant agent Substances 0.000 description 1
- 229960000805 nalbuphine Drugs 0.000 description 1
- NETZHAKZCGBWSS-CEDHKZHLSA-N nalbuphine Chemical compound C([C@]12[C@H]3OC=4C(O)=CC=C(C2=4)C[C@@H]2[C@]1(O)CC[C@@H]3O)CN2CC1CCC1 NETZHAKZCGBWSS-CEDHKZHLSA-N 0.000 description 1
- 229960002009 naproxen Drugs 0.000 description 1
- CMWTZPSULFXXJA-VIFPVBQESA-N naproxen Chemical compound C1=C([C@H](C)C(O)=O)C=CC2=CC(OC)=CC=C21 CMWTZPSULFXXJA-VIFPVBQESA-N 0.000 description 1
- 239000004081 narcotic agent Substances 0.000 description 1
- 229960000801 nelarabine Drugs 0.000 description 1
- IXOXBSCIXZEQEQ-UHTZMRCNSA-N nelarabine Chemical compound C1=NC=2C(OC)=NC(N)=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@@H]1O IXOXBSCIXZEQEQ-UHTZMRCNSA-N 0.000 description 1
- 229960000884 nelfinavir Drugs 0.000 description 1
- QAGYKUNXZHXKMR-HKWSIXNMSA-N nelfinavir Chemical compound CC1=C(O)C=CC=C1C(=O)N[C@H]([C@H](O)CN1[C@@H](C[C@@H]2CCCC[C@@H]2C1)C(=O)NC(C)(C)C)CSC1=CC=CC=C1 QAGYKUNXZHXKMR-HKWSIXNMSA-N 0.000 description 1
- 229960003512 nicotinic acid Drugs 0.000 description 1
- 235000001968 nicotinic acid Nutrition 0.000 description 1
- 239000011664 nicotinic acid Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 229960001199 olmesartan medoxomil Drugs 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229960003752 oseltamivir Drugs 0.000 description 1
- VSZGPKBBMSAYNT-RRFJBIMHSA-N oseltamivir Chemical compound CCOC(=O)C1=C[C@@H](OC(CC)CC)[C@H](NC(C)=O)[C@@H](N)C1 VSZGPKBBMSAYNT-RRFJBIMHSA-N 0.000 description 1
- 229960002739 oxaprozin Drugs 0.000 description 1
- OFPXSFXSNFPTHF-UHFFFAOYSA-N oxaprozin Chemical compound O1C(CCC(=O)O)=NC(C=2C=CC=CC=2)=C1C1=CC=CC=C1 OFPXSFXSNFPTHF-UHFFFAOYSA-N 0.000 description 1
- 229960002085 oxycodone Drugs 0.000 description 1
- 229960002369 oxyphencyclimine Drugs 0.000 description 1
- 229960002740 oxyphenonium Drugs 0.000 description 1
- 229960001057 paliperidone Drugs 0.000 description 1
- 229960000402 palivizumab Drugs 0.000 description 1
- 229960005019 pantoprazole Drugs 0.000 description 1
- 229960001789 papaverine Drugs 0.000 description 1
- 229960005489 paracetamol Drugs 0.000 description 1
- 239000000734 parasympathomimetic agent Substances 0.000 description 1
- 230000001499 parasympathomimetic effect Effects 0.000 description 1
- 229940005542 parasympathomimetics Drugs 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 229960005079 pemetrexed Drugs 0.000 description 1
- QOFFJEBXNKRSPX-ZDUSSCGKSA-N pemetrexed Chemical compound C1=N[C]2NC(N)=NC(=O)C2=C1CCC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 QOFFJEBXNKRSPX-ZDUSSCGKSA-N 0.000 description 1
- VOKSWYLNZZRQPF-GDIGMMSISA-N pentazocine Chemical compound C1C2=CC=C(O)C=C2[C@@]2(C)[C@@H](C)[C@@H]1N(CC=C(C)C)CC2 VOKSWYLNZZRQPF-GDIGMMSISA-N 0.000 description 1
- 229960005301 pentazocine Drugs 0.000 description 1
- 229960004851 pergolide Drugs 0.000 description 1
- YEHCICAEULNIGD-MZMPZRCHSA-N pergolide Chemical compound C1=CC([C@H]2C[C@@H](CSC)CN([C@@H]2C2)CCC)=C3C2=CNC3=C1 YEHCICAEULNIGD-MZMPZRCHSA-N 0.000 description 1
- 239000000810 peripheral vasodilating agent Substances 0.000 description 1
- 229960002116 peripheral vasodilator Drugs 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 229960000482 pethidine Drugs 0.000 description 1
- 229960000964 phenelzine Drugs 0.000 description 1
- 229960002895 phenylbutazone Drugs 0.000 description 1
- VYMDGNCVAMGZFE-UHFFFAOYSA-N phenylbutazonum Chemical compound O=C1C(CCCC)C(=O)N(C=2C=CC=CC=2)N1C1=CC=CC=C1 VYMDGNCVAMGZFE-UHFFFAOYSA-N 0.000 description 1
- WCMIIGXFCMNQDS-IDYPWDAWSA-M piperacillin sodium Chemical compound [Na+].O=C1C(=O)N(CC)CCN1C(=O)N[C@H](C=1C=CC=CC=1)C(=O)N[C@@H]1C(=O)N2[C@@H](C([O-])=O)C(C)(C)S[C@@H]21 WCMIIGXFCMNQDS-IDYPWDAWSA-M 0.000 description 1
- 229960002702 piroxicam Drugs 0.000 description 1
- QYSPLQLAKJAUJT-UHFFFAOYSA-N piroxicam Chemical compound OC=1C2=CC=CC=C2S(=O)(=O)N(C)C=1C(=O)NC1=CC=CC=N1 QYSPLQLAKJAUJT-UHFFFAOYSA-N 0.000 description 1
- 230000036470 plasma concentration Effects 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- GNSKLFRGEWLPPA-UHFFFAOYSA-M potassium dihydrogen phosphate Chemical compound [K+].OP(O)([O-])=O GNSKLFRGEWLPPA-UHFFFAOYSA-M 0.000 description 1
- 239000008057 potassium phosphate buffer Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 229960003089 pramipexole Drugs 0.000 description 1
- FASDKYOPVNHBLU-ZETCQYMHSA-N pramipexole Chemical compound C1[C@@H](NCCC)CCC2=C1SC(N)=N2 FASDKYOPVNHBLU-ZETCQYMHSA-N 0.000 description 1
- 229960001233 pregabalin Drugs 0.000 description 1
- AYXYPKUFHZROOJ-ZETCQYMHSA-N pregabalin Chemical compound CC(C)C[C@H](CN)CC(O)=O AYXYPKUFHZROOJ-ZETCQYMHSA-N 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 150000003180 prostaglandins Chemical class 0.000 description 1
- 229960005206 pyrazinamide Drugs 0.000 description 1
- IPEHBUMCGVEMRF-UHFFFAOYSA-N pyrazinecarboxamide Chemical compound NC(=O)C1=CN=CC=N1 IPEHBUMCGVEMRF-UHFFFAOYSA-N 0.000 description 1
- 229960004431 quetiapine Drugs 0.000 description 1
- URKOMYMAXPYINW-UHFFFAOYSA-N quetiapine Chemical compound C1CN(CCOCCO)CCN1C1=NC2=CC=CC=C2SC2=CC=CC=C12 URKOMYMAXPYINW-UHFFFAOYSA-N 0.000 description 1
- 229960001778 rabeprazole sodium Drugs 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 229960000620 ranitidine Drugs 0.000 description 1
- VMXUWOKSQNHOCA-LCYFTJDESA-N ranitidine Chemical compound [O-][N+](=O)/C=C(/NC)NCCSCC1=CC=C(CN(C)C)O1 VMXUWOKSQNHOCA-LCYFTJDESA-N 0.000 description 1
- 229960000213 ranolazine Drugs 0.000 description 1
- 208000002574 reactive arthritis Diseases 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 229960002917 reteplase Drugs 0.000 description 1
- 108010051412 reteplase Proteins 0.000 description 1
- 229960000329 ribavirin Drugs 0.000 description 1
- HZCAHMRRMINHDJ-DBRKOABJSA-N ribavirin Natural products O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1N=CN=C1 HZCAHMRRMINHDJ-DBRKOABJSA-N 0.000 description 1
- 229960000885 rifabutin Drugs 0.000 description 1
- 229960000311 ritonavir Drugs 0.000 description 1
- NCDNCNXCDXHOMX-XGKFQTDJSA-N ritonavir Chemical compound N([C@@H](C(C)C)C(=O)N[C@H](C[C@H](O)[C@H](CC=1C=CC=CC=1)NC(=O)OCC=1SC=NC=1)CC=1C=CC=CC=1)C(=O)N(C)CC1=CSC(C(C)C)=N1 NCDNCNXCDXHOMX-XGKFQTDJSA-N 0.000 description 1
- 229940071773 rozerem Drugs 0.000 description 1
- 235000012045 salad Nutrition 0.000 description 1
- 201000000980 schizophrenia Diseases 0.000 description 1
- 229950009846 scopolamine butylbromide Drugs 0.000 description 1
- 229940125723 sedative agent Drugs 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000003369 serotonin 5-HT3 receptor antagonist Substances 0.000 description 1
- GZKLJWGUPQBVJQ-UHFFFAOYSA-N sertindole Chemical compound C1=CC(F)=CC=C1N1C2=CC=C(Cl)C=C2C(C2CCN(CCN3C(NCC3)=O)CC2)=C1 GZKLJWGUPQBVJQ-UHFFFAOYSA-N 0.000 description 1
- 229960000652 sertindole Drugs 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 229940083037 simethicone Drugs 0.000 description 1
- 230000004622 sleep time Effects 0.000 description 1
- 229940083618 sodium nitroprusside Drugs 0.000 description 1
- 229960005077 sodium picosulfate Drugs 0.000 description 1
- GOZDTZWAMGHLDY-UHFFFAOYSA-L sodium picosulfate Chemical compound [Na+].[Na+].C1=CC(OS(=O)(=O)[O-])=CC=C1C(C=1N=CC=CC=1)C1=CC=C(OS([O-])(=O)=O)C=C1 GOZDTZWAMGHLDY-UHFFFAOYSA-L 0.000 description 1
- 229960000776 sodium tetradecyl sulfate Drugs 0.000 description 1
- UPUIQOIQVMNQAP-UHFFFAOYSA-M sodium;tetradecyl sulfate Chemical compound [Na+].CCCCCCCCCCCCCCOS([O-])(=O)=O UPUIQOIQVMNQAP-UHFFFAOYSA-M 0.000 description 1
- 239000012453 solvate Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 235000010356 sorbitol Nutrition 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000008143 stimulant laxative Substances 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 229960005202 streptokinase Drugs 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- MNQYNQBOVCBZIQ-JQOFMKNESA-A sucralfate Chemical compound O[Al](O)OS(=O)(=O)O[C@@H]1[C@@H](OS(=O)(=O)O[Al](O)O)[C@H](OS(=O)(=O)O[Al](O)O)[C@@H](COS(=O)(=O)O[Al](O)O)O[C@H]1O[C@@]1(COS(=O)(=O)O[Al](O)O)[C@@H](OS(=O)(=O)O[Al](O)O)[C@H](OS(=O)(=O)O[Al](O)O)[C@@H](OS(=O)(=O)O[Al](O)O)O1 MNQYNQBOVCBZIQ-JQOFMKNESA-A 0.000 description 1
- 229960004291 sucralfate Drugs 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229940056501 technetium 99m Drugs 0.000 description 1
- 229960005311 telbivudine Drugs 0.000 description 1
- IQFYYKKMVGJFEH-CSMHCCOUSA-N telbivudine Chemical compound O=C1NC(=O)C(C)=CN1[C@H]1O[C@@H](CO)[C@H](O)C1 IQFYYKKMVGJFEH-CSMHCCOUSA-N 0.000 description 1
- 229960000216 tenecteplase Drugs 0.000 description 1
- 229960005333 tetrabenazine Drugs 0.000 description 1
- 230000036962 time dependent Effects 0.000 description 1
- 239000003053 toxin Substances 0.000 description 1
- 231100000765 toxin Toxicity 0.000 description 1
- 108700012359 toxins Proteins 0.000 description 1
- GYDJEQRTZSCIOI-LJGSYFOKSA-N tranexamic acid Chemical compound NC[C@H]1CC[C@H](C(O)=O)CC1 GYDJEQRTZSCIOI-LJGSYFOKSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- LLPOLZWFYMWNKH-UHFFFAOYSA-N trans-dihydrocodeinone Natural products C1C(N(CCC234)C)C2CCC(=O)C3OC2=C4C1=CC=C2OC LLPOLZWFYMWNKH-UHFFFAOYSA-N 0.000 description 1
- 229960003741 tranylcypromine Drugs 0.000 description 1
- 229960003167 tridihexethyl Drugs 0.000 description 1
- NPRHVSBSZMAEIN-UHFFFAOYSA-N tridihexethyl Chemical group C=1C=CC=CC=1C(O)(CC[N+](CC)(CC)CC)C1CCCCC1 NPRHVSBSZMAEIN-UHFFFAOYSA-N 0.000 description 1
- IEDVJHCEMCRBQM-UHFFFAOYSA-N trimethoprim Chemical compound COC1=C(OC)C(OC)=CC(CC=2C(=NC(N)=NC=2)N)=C1 IEDVJHCEMCRBQM-UHFFFAOYSA-N 0.000 description 1
- 229960001082 trimethoprim Drugs 0.000 description 1
- 229960001579 trimethyldiphenylpropylamine Drugs 0.000 description 1
- NSHMKXVHJBBKTN-UHFFFAOYSA-N trimethyldiphenylpropylamine Chemical compound C=1C=CC=CC=1C(CC(C)N(C)C)C1=CC=CC=C1 NSHMKXVHJBBKTN-UHFFFAOYSA-N 0.000 description 1
- 229960002431 trimipramine Drugs 0.000 description 1
- ZSCDBOWYZJWBIY-UHFFFAOYSA-N trimipramine Chemical compound C1CC2=CC=CC=C2N(CC(CN(C)C)C)C2=CC=CC=C21 ZSCDBOWYZJWBIY-UHFFFAOYSA-N 0.000 description 1
- 229960005356 urokinase Drugs 0.000 description 1
- 235000016788 valerian Nutrition 0.000 description 1
- MSRILKIQRXUYCT-UHFFFAOYSA-M valproate semisodium Chemical compound [Na+].CCCC(C(O)=O)CCC.CCCC(C([O-])=O)CCC MSRILKIQRXUYCT-UHFFFAOYSA-M 0.000 description 1
- MYPYJXKWCTUITO-LYRMYLQWSA-O vancomycin(1+) Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=C2C=C3C=C1OC1=CC=C(C=C1Cl)[C@@H](O)[C@H](C(N[C@@H](CC(N)=O)C(=O)N[C@H]3C(=O)N[C@H]1C(=O)N[C@H](C(N[C@@H](C3=CC(O)=CC(O)=C3C=3C(O)=CC=C1C=3)C([O-])=O)=O)[C@H](O)C1=CC=C(C(=C1)Cl)O2)=O)NC(=O)[C@@H](CC(C)C)[NH2+]C)[C@H]1C[C@](C)([NH3+])[C@H](O)[C@H](C)O1 MYPYJXKWCTUITO-LYRMYLQWSA-O 0.000 description 1
- 239000000811 xylitol Substances 0.000 description 1
- 235000010447 xylitol Nutrition 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 229960002675 xylitol Drugs 0.000 description 1
- 235000013618 yogurt Nutrition 0.000 description 1
- 229960001028 zanamivir Drugs 0.000 description 1
- ARAIBEBZBOPLMB-UFGQHTETSA-N zanamivir Chemical compound CC(=O)N[C@@H]1[C@@H](N=C(N)N)C=C(C(O)=O)O[C@H]1[C@H](O)[C@H](O)CO ARAIBEBZBOPLMB-UFGQHTETSA-N 0.000 description 1
- 229960002555 zidovudine Drugs 0.000 description 1
- 229960005111 zolpidem tartrate Drugs 0.000 description 1
- HDOZVRUNCMBHFH-UHFFFAOYSA-N zotepine Chemical compound CN(C)CCOC1=CC2=CC=CC=C2SC2=CC=C(Cl)C=C12 HDOZVRUNCMBHFH-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/28—Dragees; Coated pills or tablets, e.g. with film or compression coating
- A61K9/2806—Coating materials
- A61K9/2833—Organic macromolecular compounds
- A61K9/286—Polysaccharides, e.g. gums; Cyclodextrin
- A61K9/2866—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/28—Dragees; Coated pills or tablets, e.g. with film or compression coating
- A61K9/2806—Coating materials
- A61K9/282—Organic compounds, e.g. fats
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/28—Dragees; Coated pills or tablets, e.g. with film or compression coating
- A61K9/2806—Coating materials
- A61K9/288—Compounds of unknown constitution, e.g. material from plants or animals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/20—Hypnotics; Sedatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2072—Pills, tablets, discs, rods characterised by shape, structure or size; Tablets with holes, special break lines or identification marks; Partially coated tablets; Disintegrating flat shaped forms
- A61K9/2086—Layered tablets, e.g. bilayer tablets; Tablets of the type inert core-active coat
- A61K9/209—Layered tablets, e.g. bilayer tablets; Tablets of the type inert core-active coat containing drug in at least two layers or in the core and in at least one outer layer
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Botany (AREA)
- Zoology (AREA)
- Neurosurgery (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Anesthesiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Bir açıda mevcut buluş, aktif ajanın uygulanmasından bir süre sonra bir zaman noktasında bir aktif ajanın bir vuruşta salınmak üzere tasarlanmasının istendiği bir tedaviye yöneliktir. Mevcut buluş özellikle bir denek uyurken salınabilecek bir ajanın uygulanmasına yönelik uygundur. Belirli bir rejim ile belirli koşulların tedavi edilmesinin yanı sıra buluş aynı zamanda ilacın gecikmeli akabinde atımlı bir salımına yönelik yeni formülasyonları sağlar.
Description
TARIFNAME
PULSATIL ILAÇ SALIMI
Bulus Sahasi
Bir açida mevcut bulus, aktif ajanin uygulanmasindan bir süre sonra bir zaman
noktasinda bir aktif ajanin bir vurusta salinmak üzere tasarlanmasinin istendigi bir
tedaviye yöneliktir. Mevcut bulus özellikle bir kisi uyurken salinabilecek bir ajanin
uygulanmasina yönelik uygundur. Belirli bir rejim ile belirli durumlarin tedavi edilmesinin
yani sira bulus ayni zamanda ilacin gecikmeli akabinde atimli bir salimina yönelik yeni
formülasyonlari saglar.
Bulusun Altyapisi
ilaçlarin zamana-bagli salim mekanizmalari birçok fizikokimyasal ve fizikomekanik
stratejilerden faydalanan tablet, pellet ve kapsül formülasyonuna yönelik literatürde
açiklanmistir. Bu tür tüm formülasyonlarin ortak özelligi hasta tarafindan alim akabinde
sivilar ile temas araciligiyla etkinlesmesi ve ilacin uygulama akabinde önceden
belirlenen zamanda salinacak olmasidir. Yalnizca formülasyonlarin gastrik sivilar ile
temas etmesi akabinde “saat, islemeye baslar. Dozaj biriminin gecikme süresi boyunca
GI sistemi boyunca hareket edecek olmasi nedeniyle, ilaç saliminin zorunlu olarak
bilinmeyen bir GI sistemi alaninda olacaginin anlasilacak olmasina ragmen, ilaç salimi
akabinde tahmin edilen bir zamanda gerçeklesir. Bu tür formülasyon stratejileri
kullanilarak, kronoterapötik ilkelere göre ilaç salabilen ve hastalik durumlarinin
sirkadiyen ritmine salim hedefleyebilen dagitim sistemleri tasarlamak mümkün olacaktir
(Stevens HNE, Chronopharmaceutical Drug Delivery. J Pharm Pharmac., 50 (s) 5
(1998) and Ghimire M , European Journal of Phannaceutics and Biopharmaoeutics. 67
(2007)). Ancak, teknikteki formülasyonlarin birçogu ilacin üretim maliyetine eklenen
ve/veya ilacin yanlis/uygun olmayan uygulamasina neden olan arizaya maruz kalabilen
kompleks yapilara dayanir.
Yukaridaki dezavantajlardan en az birini gidermek ve/veya hafifletmek mevcut bulusun
amaçlari arasindadir.
Kolay bir sekilde ve/veya ucuz bir sekilde üretilebilen ve aktif bir ajanin kisa bit atimda
uygulanmasina akabinde bir gecikme süresi akabinde uygulanmasina olanak saglayan
bir formülasyon saglamak mevcut bulusun amaçlari arasindadir.
Bulusun kisa açiklamasi
Mevcut bulusçular, farmasötik olarak aktif içerik maddesinin gecikmeli bir salimi
akabinde ajanin atimli bir dagitimi gerçeklestirilebilecek sekilde örnegin farmasötik
olarak aktif ajanin bir denege uygulanabilmesine yönelik bir ihtiyaç fark etmistir. Bu
sorun, istemler 1-9 ile tanimlandigi üzere bir tablet formülasyonu ile çözülür. Bunun
teknikteki önceki cihaz/yöntemler kullanilarak mümkün olmasina ragmen, bu tür birçok
cihaz/yöntem oldukça komplekstir ve daha basit bir presle-kaplanan tablet
formülasyonu saglamakta belirgin avantaj vardir.
Özellikle tercih edilen bir düzenleme, yaygin olarak uykuyu sürdürememe olarak
adlandirilan gece boyunca uyanan ancak baslangiç olarak uykuya dalmak konusunda
sifir veya az bir soruna sahip olan deneklerin tedavi edilmesiyle ilgilidir. Bu nedenle
tercih edilen bir düzenlemede mevcut bulusun formülasyonlari, uykuyu
sürdürememenin tedavi edilmesine yöneliktir. Bu tür formülasyonlar bu nedenle uykuya
sebep olmaya ve/veya bunu kolaylastirmaya yönelik farmasötik olarak aktif bir ajani
içerir. Bu tipik olarak benzodiazepin, kloral hidrat, melatonin ve bunun analoglari,
zolpidem, zopiklon veya zaleplon gibi yatistirici veya hipnotik bir ajan olabilir.
Bu nedenle birinci bir açida mevcut bulus, uykuyu sürdürememenin tedavi edilmesine
yönelik presle kaplanan bir tabletin bir bileseni olarak formüle edilen bir yatistirici veya
hipnotik ajan gibi uykuya sebep olan ve/veya bunu sürdüren bir formülasyon saglar,
burada formülasyonun bir denegin uyumaya gitmesinden hemen önce (diger bir
ifadeyle bir kisi 6-10 saat gibi uzun bir uyku periyoduna yönelik yataga gittiginde
böylece daha kisa uyuma periyotlarindan farklidir) uygulanmasi amaçlanir ve burada
hipnotik ajan, denege formülasyonun uygulanmasinda sonraki 1.5-8 saat arasinda bir
periyot boyunca formülasyondan büyük oranda salinmaz ve bundan sonra ajan,
veya 10-30 dakika içinde salinacak sekilde bir atim olarak formülasyondan salinir.
Diger bir açida uykuyu sürdürememenin tedavi edilmesine yönelik bir yöntem saglanir,
yöntem denegin uyumayi amaçlamasindan hemen önce bir denege yatistirici veya
hipnotik bir ajan gibi uykuya sebep olan bir ajani içeren presle kaplanmis bir tabletin
uygulanmasini içerir, burada formülasyon, formülasyonun uygulanmasinin akabindeki
1.5-8 saat boyunca ilacin salimini büyük oranda geciktirir ve bundan sonra ilaç, 10-45
veya 10-30 dakika gibi 5-80 dakikalik bir periyot üzerinde bir atim içinde salinir. Aktif
ajanin gecikmeli salimi, aktif ajani içeren çekirdegi çevreleyen gecikmeli bir salim
katmanini içeren presle kaplanmis bir tabletin saglanmasiyla gerçeklestirilir. Gecikmeli
salim katmani, bir mum ve LH-11 olan düsük sübstitüeli bir hidroksipropil selüloz (L-
HPC) içerir. Mevcut bulus aktif bir ajanin gecikmeli akabinde atimli bir salimina yönelik
presle kaplanan birformülasyon saglar, tablet asagidakileri içerir
(a) bir eksipiyan(lar) ile birlikte aktif ajanlari içeren bir çekirdek; ve
(b) çekirdegin etrafini saran ve 40:60 ila 60:40 w/w'lik bir oranda bir mum ve
LH-11 içeren bir gecikmeli salim katmani; burada gecikmeli salim katmani bir
kisi tarafindan tabletin uygulanmasindan senra 1.5 - 8 saat boyunca çekirdek
içindeki aktif ajanin salimini büyük oranda geciktirir ve bundan sonra aktif
ajanin çekirdekten atimli bir salimi meydana gelir, böylece çekirdekteki aktif
Yukaridaki açinin aktif ajanlari, gecikmeli akabinde atimli salimin istendigi herhangi bir
aktif ajani içerir. Bulusun tercih edilen bir düzenlemesinde, aktif ajan farmasötik olarak
kabul edilebilir bir aktif ajandir ve farmasötik ve veterinerlik aktif ajanlarini (genellikle
ilaçlar olarak refere edilir) içerir. Diger düzenlemelerde, aktif ajan kimyasal tarim
ajanlari (örnegin gübreler, herbisitler, pestisitler ve fungisitler), imha etme endüstrisinde
kullanilan aktif ajan (örnegin toksinler ve zehirler) ve endüstriyel üretimde kullanilan
aktif ajanlari (örnegin katalizörler veya katalitik söndürücüler) içerir.
Mevcut bulusun presle kaplanan tabletleri asagidaki durumlar/bozukluklar veya
hastaliklarin bir veya daha fazlasini tedavi etmek üzere kullanilabilir:
Merkezi Sinir Sistemi hastaliklari, örnegin Nörojenik agri, felç, demans,
Alzheimer hastaligi, Parkinson hastaligi, nöronal dejenerasyon, menejit, spinal
kord hasari, serebral vazospazm, amiyotrofik lateral skleroz
Kardiovasküler hastalik, hipertansiyon, ateroskleroz, anjin, arteriyel
obstrüksiyon, periferik arter hastaligi, miyokardiyal patoloji, Aritmi, Akut
Miyokard Enfakrtüs, Anjin, Kardiyomiyopati, Konjestif kalp yetmezligi, Koroner
arter hastaligi (CAD), Karotis arter hastaligi, Endokardit, Hiperkolesterolemi,
hiperlipidemi, Periferik arter hastaligi (PAD)
Genitoüriner Rahatsizliklar; erektil disfonksiyon, üreriner organ hastaliklari
benign prostat hipertrofisi (BPH), Renal tübüler asidoz, diyabetik nefropati,
glomerülonefrit, glomerüloskleroz, üriner sistem enfeksiyonu, fekal inkontinans
Göz hastalklari glakom, blefarit, oküler hipertansiyon, retinopati, konjonktivit,
sklerit, retinit, keratit, kornea ülseri, iritis, korioretinal inflamasyon, makuler
ödem, Kseroftalmi
Pulmoner hastalik astim, pulmoner hipertansiyon, akut solunum sikintisi
sendromu, COPD, amfizem, pnömoni, tüberküloz, bronsit, Akut Bronsit,
Bronsektazi, Bronsiyolit, Bronkopulmoner displazi, Bisinoz, Koksidioidomikoz
(Koksi), Kistik Fibroz, Grip, Akciger Kanseri, Mezotelyoma
Metabolik hastaliklar Hiperkalsiüri, Hiperglisemi, Hiperinsülinemik hipoglisemi,
Hiperinsülinizm, Hiperüsinüri, Hipoglisemi
Eksokrin ve Endokrin; Addison hastaligi, Hipoaldosteronizm, cushing
sendormu, diyabet, Guatr, Hipertiroidzm, Hipotiroidzm, Tiroidit, pankreatit
Hepatik bozukluklar, Hepatit, Alkolik-olmayan yagli karaciger hastaligi, siroz,
hepatik kanser, Primer sklerozan kolanjit, primer biliyer siroz, Budd-Chiari
sendormu,
Otoimmün ve Inflamatuar hastaliklar, multipl skleroz, romatoid artrit,
psöriyazis, diyabet, sarkoidoz, Addison Hastaligi, Saçkiran, Amyotrofik Lateral
Skleroz, Ankilozan Spondilit, poliartiküler Artrit, Atopik alerji, topik Dermatit,
Otoimmün hepatit, Çölyak hastaligi, Sagaz hastaligi, Çölyak hastaligi, Cogan
sendromu, Chron Hastaligi, Cushing Sendormu, Diyabet tip 1, Endometriyoz,
Eozinofilik fasitt, Fibromiyalji/Fibromiyozit, Gastrit, Glomerülonefrit, Graves
hastaligi Guillain-Barré sendromu (GBS), Hashimoto ensefalit, Hashimoto
tiroiditi, Hemolitik anemi, Idiyopatik Inflamatuar Demiyelinizan Hastaliklar,
Idiyopatik pulmoner fibroz, interstisyel sistit, Juvenil idiyopatik artrit, Juvenil
romatoid artrit, Kawasaki Hastaligi, Iiken sklerozus, Lupus eritematozus,
Me'niere hastaligi, Miyastenya gravis, miyozit, Narkolepsi, Pernisiyöz anemi,
perivenöz ensefalomiyelit, Polimiyaljiya romatika, Primer biliyer siroz, Psoriatik
artrit, Reiter sendromu, Romatoid ates, Sarkoidoz, Sizofreni, Sjögren
sendormu, Spondiloartropati, Ülseratif kolit
Musculoskeletal bozukluklar: osteoartrit, orteoporoz, Osteonekroz, Artrit,
Paget Hastaligi, Bursit, Kostokondrit, Tendonit
Cilt bozukluklari; Akne, alopesi, andidiyaz, selülit, dermatit, egzema,
epidermolizis bülloza, eritrazma, uçuk, erisipel, Folikülit, impetigo, mantar
hastaligi, skabiyez, Tinea, Trikomikoz
ENT bozukluklari; Otit, sinüzit, Iarinjit, faranjit, Iarinjit, meniere hastaligi,
Digerleri: akut ve kronik agri, viral enfeksiyon, kanser, Iarenjit, mastoidit,
mirinjit, otitis media, rinit, sinüzit, Sialadenit, Retrofarengeal apse,
Tonsilofarenjit,
Gastro-intestinal bozukluklar
Irritabl bagirsak sendromu (IBS), nekrotizan enterokolit (NEC) ülser-olmayan dispepsi,
kronik intestinal psödo-obstrüksiyon, fonksiyonel dispepsi, kolonik psödo-
obstrüksiyonduedenogastrik reflü, gastroözofajeal reflü hastaligi, Ileus inflamasyonu,
gastroparezi, mide yanmasi, kabizlik - (örnegin opoidler gibi ilaçlara yönelik kullanim ile
iliskili kabizlik), kolorektal kanser, kolonik polipler, divertikülit, kolorektal kanser, Barrett
Özefagusu, Sindirim Sisteminde Kanama, Çölyak Hastaligi, Kolon Polipleri, Kabizlik,
Crohn Hastaligi, Siklik Kusma Sendromu, Gecikmeli Mide Bosalmasi (Gastroparezi),
Diare, Divertikülozis, Duodenal Ülserler, Feçes Inkontinansi, Safra tasi, Sindirim
Sisteminde Gaz, Gastrit, Gastroözofajeal Reflü Hastaligi (GERD), Mide yanmasi,
Hiyatus Hemisi, Hemokromatoz, Hemoroid, Hiyatus Hemisi, Hirschsprung Hastaligi,
Hazimsizlik, Inguinal Herni, Laktoz Intoleransi, Peptik Ülserler, Polipler, Porfiri, Primer
Biliyer Siroz, Primer Sklerozan Kolanjit, Proktit, Hizli mide Bosalmasi, Kisa Bagirsak
Sendromu, Mide Ülserleri, ülseratif Kolit, Ülserler, Whipples Hastaligi
Bulusun farmasötik ve veterinerlikle ilgili uygulamalarinda kullanima yönelik örnek aktif
ajanlar analjezikler, anestetikler, antikonvülsanlar, antiyabetik ajanlar, antihistaminler,
anti-enfektifler, antineoplastikler, antiparkinson ajanlar, antiromatizmal ajanlar, istah
uyaricilar, istah bastiricilar, kan düzenleyiciler, kemik metabolizmasi düzenleyicileri,
kardiyosküler ajanlar, merkezi sinir sistemi depresanlari, merkezi sinir sistemi
uyaricilari, dekonjestanlar, dopamin reseptörü agonistleri, electrolitler, gastrointestinal
ajanlar, immunomodülatörler, kas gevseticiler, uyusturucular, parasempatomimetikler,
sempatomimetikler, yatistiricilar ve hipnotikleri içerir.
Söz konusu aktif ajan veya ajanlar asagidaki unsurlardan segilebilir:
Gastro Ilaçlar
Antasitler - alüminyum hidroksit, magnezyum karbonat, magnezyum trisilikat,
hidrotalsit, simetikon alginatlari,
Antispazmodikler - atropin sülfat, disikloverin hidroklorid, hiyosin bütilbromin,
propantelin bromür, alverin sitrat, mebeverin hidroklorid,
Motilite uyaricilar - metoklorpramid, domperidon
H2 - Reseptör antogonistleri - Simetidin, famotidinnizatidin, ranitidin
Selatlar - Tripotasyum disitratbismutat, sukralfat.
Prostaglandin analoglari - misoprostol
Aminosalisilatlar - balsazid sodyum, mesalazin, olsalazin, sülfasalazin
Kortikosteroidler - beklometazon dipropinat, budenosid, hidrokortizon,
pednisolon,
Immün yaniti etkileyenler - siklosporin, merkaptopürin, metotreksat,
adalimumab, infliksimab
Uyarici Laksatifler - bisakodil, dantron, dokusat, sodyum pikosülfat,
Biliyer bilesim ve akisi etkileyen ilaçlar - ursodeoksikolik asit
Safra asiti sekestranlari - kolestramin,
Oksifensiklimin, Kamilofin, Mebeverin, Trimebütin, Rosiverin, Disikloverin,
Diheksiverin, Difemerin, Piperidolat Benzilon, Mepenzolat, Pipenzolat,
Glikopironyum, Oksifenonyum, Fentienat, Mentantelin, Propantelin, Otilonyum
bromür, Tridiheksetil, Izopropamid, Heksosikliyum, Poldin, Bevonyum,
Difemanil, Tiemonyum iyodür, Prifinyum bromür, Timepidyum bromür,
Fenpiverinyum Papaverin, Drotaverin, Moksaverin 5-HT3 antagonistleri
(Alosetron, Silansetron), 5-HT4 agonistleri (Mosaprid, Prukaloprid, Tegaserod)
Fenpipran, Diizopromin, Klorbenzoksamin, Pinaveryum, Fenoverin, Idanpramin,
Proksazol, Alverin, Trepibuton, Izometepten, Karoverin, Floroglusinol, Silikonar,
Trimetildifenilpropilamin Atropin, Hiyosiyamin Skopolamin (Bütilskopolamin,
Metilskopolamin), Metilatropin, Fentonyum, Simetropyum bromür primer
dopamin antagonistleri (Metoklopramid/Bromoprid, Kleboprid, Domperidon,
Alizaprid), 5-HT4 agonistleri (Sinitaprid, Sisaprid),
Proton pompasi inhibitörleri Omeprazol, Iansoprazol, pantoprazol,
esomeprazol, rabeprazole sodyum,
opioidler ve opioid reseptörü antagonistleri - örnegin kodein, morfin,
Analjezik
Asetaminofen, Diklofenak, Diflunisal, Etodolak, Fenoprofen, Flurbiprofen, Ibuprofen,
Nabumeton, Naproksen, Oksaprozin, Fenilbütazon, Piroksikam, Sulindak, Tolmetin,
Selekoksib, Buprenorfin, Butorfanol, Kodein, Hidrokodon. Hidromorfon. Levorfanol,
Meperidin, Metadon, Morfin, Nalbufin. Oksikodon, Oksimon'on. Pentazosin,
Propoksifen, Tramadol, kodein
Uzku ilaçlari
Hipnotikler - Nitrazepam, Flurazepam, Loprazolam, Lormetazepam, Temazepam,
Zaleplon, Zolpidem, Zopiklon, Kloral Hidrat, Triklofos, Klometiazol, Kuazepam,
triazolam Estazolam Klonazepam Alprazolam, Eszopiklon. Rozerem, Trazodon,
Amitriptilin Doksepin, Benzodiazepin ilaçlar, melatonin, difenhidramin ve Kedi otu gibi
bitkisel ilaçlar
Kardiovasküler ilaçlar
Kardiak glikosidler - Digoksin, digitoksin,
Fosfodiesteraz Inhibitörleri - enoksimon, milrinon
Tiazidler ve ilgili diüretikler -bendroflumetiazid, klortalidon, siklopentiazid,
inapamid, metolazon, ksipamid
Diüretikler - furosemid, bumetanid, torasemid,
Potasyum koruyucu diüretikler ve aldosteron antagonistleri - amilorid
hidroklorid, triamteren, weplerenon, spironolakton.
Osmotik diüretikler- manitol
Arimiye yönelik ilaçlar -adenosin, amiodaron hidroklorid, disopiramid,
flekainid asetat, propafenon hidroklorid, Iidokain hidroklorid,
Beta adrenoreseptör engelleyici ilaçlar - propanalol, atenolol, asebütolol,
bisoprolol, fumarat, karvedilol, seliprolol, esmolol, Iebatolol, metoprolol tartrat,
nadolol, nebivolol, oksprenolol, pindolol, solatol, timolol,
Hipertansiyon -ambrisentan, bosentan. diazoksid, hidralazin, iloprost,
minoksidil, sildenafil, sitaksentan, sodyum nitroprussid, klonidin, metildopa,
moksonidin, guanetidin monosülfat, doksazosin, indoramin, prazosin, terazosin,
fenoksibenzamin, fentolamin mesilat,
Renin-anjiyotensin sistemi etkileyen ilaçlar - Kaptropril, Silazapril, Enalapril
Maleat, Fosinopril, Imidapril. Lisinopril. Moeksipril. Perindopril Erbumin, Kinapril,
Ramipril, Trandolapril, Kandesartan Sileksetil, Eprosartan, Irbesartan, Losartan,
Olmesartan Medoksomil, Telmisartan, Valsartan, Aliskiren.
Nitratlar, kalsiyum kanal Blokerleri ve antianjinal ilaçlar-Gliseril trinitrat,
Izosorbid Dinitrat, Izosorbid Mononitrat, Amlodipin, Diltiazem, Felodipin,
Isradipin, Lasidipin, Lerkanidipin, Nikardipin, Nifedipin, Nimodipin, Verapamil,
Ivabradin, Nikorandil, Ranolazin,
Periferik Vazodilatörler ve iliskili ilaçlar -Silostazol, Inositol Nikotinat,
Moksisilit, Naftidrofuril Oksalat, Pentoksifyilin,
Sempatomimetikler -Dopamin, Dopeksamin, Efedrin, Metaraminol,
Noradrenalin Asit Tartrat, Norefidrin Bitartrat, Fenilefidrin,
Antikoagülanlar ve Protamin - Heparin, Bemiparin, Dalteparin, Enoksaparin,
Tinzaparin, Danaparoid, Bivalirudin, Lepirudin, Epoprostenol. Fondaprinuks,
Varfarin, Asenokoumarol, Fenindion, Dabigatran Eteksilat, Rivaroksaban,
Protamin Sülfat,
Antiplatelet Ilaçlari - Absiksimab, Asprin, Klopidogrel, Dipiridamol, Eptifibatid,
Prasugrel, Tirofiban,
Fibrinolitik ve antifibrinolitik Ilaçlar -Alteplaz, Reteplaz, Streptokinaz,
Tenekteplaz, Ürokinaz, Etamsilat, Traneksamik Asit.
Lipid Düzenleyici Ilaçlar -Atorvastatin, Fluvastatin, Pravastatin, Rosuvastatin,
Simvastatin, Kolesevam, Kolestiramin, Kolestipol, Ezetimib, Bezafibrat,
Siprofibrat, Fenofibrat, Gemfibrozil, Asipmoks, Niktotinik Asit, Omega üç yag
asiti bilesikleri, Etanolamin Oleat, Sodyum Tetradesil Sülfat.
CNS Ilaçlari - Benperidol, Klorpromazin, Flupentiksol, Haloperidol, Levomepromazin,
Perisiazin, Perfenazin, Pimozid, Proklorperazin, Promazin, Sülpirid, Trifluoperazin,
Zuklopentiksol, Amisülprid, Aripiprazol, Klozapin, Olanzapin, Paliperidon, Ketiapin,
Riperidon, Sertindol, Zotepin, Flupentiksol, Flufenazin, Olanzapin Embonat, Pipotiazin
Palmitat, Risperidon, Zuklopentiksol Dekanoat, Karbamazepin, Valproat, Valproik asit,
Lityum Karbonat, Lityum Sitrat, Amitriptilin, Klomipramin, Dosulepin. Imipramin,
Lofepramin, Nortriptilin, Trimipramin, mianserin, Trazodon, Fenelzin, Izokarboksazid,
Tranilsipromin, Moklobemid, Sitalopram, Essitalopram, Fluoksetin, Fluvoksamin,
Paroksetin, Sertralin, Agomelatin, Duloksetin, Flupentiksol, Mirtazapin, Reboksetin,
Tritofan, Venflaksin, Atomoksetin, Deksametamin, Metilfenidat, Modafinil,
Eslikarbazepin, Okarbazepen, Etosüksimid, Gabapentin, Pregabalin, Lakosamid,
Lamotrigin, Levetirasetam, Fenobarbital, Primidon, Fenitoin, Rufinamid, Tiagabin,
Topiramat, Vigabatrin, Zonisamie, ropinirol, Rotigotin, Ko-Beneldopa, Levodopa, K0-
Kareldopa, Rasagilin, Selegilin, Entakapon, Tolkapon, Amantidin, Orfenadrin,
Prosiklidin, Trihesifenidil, Haloperidol, Pirasetam, Riluzol, Tetrabenazin, Akamprosat,
Disülfiram, Bupropiyon, Varenisilin, Buprenorfin, Lofeksidin, Donepezil, Galantamin,
Memantin, Rivastigimin.
Anti-Enfektivler- Benzilpenisilin, Fenoksimetilpenisilin, Flukloksasilin, Temosilin,
Amoksisilin, Ampisilin, Ko-Amoksiklav, Ko-Fluampisil, Piperasilin, Tikarsilin,
Pivmesilinam, Sefalosporinler, Sefaklor, Sefadroksil, Sefaleksin, Sefiksim, Sefotaksim,
Sefradin, Seftazidim, Sefuroksim, Ertapenem. Imipenem, Meropenem, Aztreonam,
Tetrasiklin, Demeklosiklin, Doksosiklin, Limesiklin, Minosiklin, Oskitetrasiklin, Tigesiklin,
Gentamisin, Amikasin, Neomisin, Tobramisin, Eritromisin, Azitromisin, Klaritromisin,
Telitromisin, Klindamisin, Kloramfenikol, Fusidik Asit, Vankomisin, Teikoplanin,
Daptomisin, Linezolid, Kinupristin, Kolistin, Ko-Trimoksazol, Sülpadiazin, Trimetoprim
Kapreomisin, Sikloserin, Etambütol, Izoniazid, Pirazinamid, Rifabutin, Rifampisin,
Streptomisin, Dapson, Klofazimin, Metronidazol, Tinidazol, Siproflaksasin,
Levoflaksasin, Moksifloksasin, Nalidiksik Asit, Norflaksin, Orflaksasin, Nitrofurantoin,
Metenamin Hippürat, Amfoterisin, Anidulafungin, Kaspofungin, Flukonazol, Flusitosin,
Griseofluvin, Itrakonzol, Ketokonazol, Mikafungin, Nistatin, Posakonazol, Terbinafin,
Vorikonazol, Abakavir, Didanosin, Emtrisitabin, Lamivudin, Stavudin, Tenofovir
Disoproksil, Zidovudin, Atazanavir, Darunavir, Fosamprenavir, Indinavir. Lopinair,
Nelfinavir, Ritonavir, Sakinavir, Tipranavir. Efavirenz, Etravirin, Nevarapin, Enfuvirtid,
Maravirok, Raltegravir, Asiklovir, Famsiklovir, Inosin Pranobeks, Valasiklovir, Sidofovir,
Gangsiklovir, Foskarnet, Valgangsiklovir, Adefovir Dipivoksil, Entekavir, Telbivudin,
Amantadin, Oseltamivir, Zanamivir, Palivizumab, Ribavirin, Artemeter, Klorokin,
Meflokin Primakin, Proguanil, Pirimetamin, Kinin, Doksisiklin, Diloksanid Furoat,
Metronidaziol, Tinidazol, Mepakrin Sodyum Stiboglukonat, Atovakuon, Pentamidin
Izetionat, Mebendazol, Piperazin,
Digerleri:
Benztropiprocsiklidin biperiden, Amantadin Bromokriptin Pergolid Entakapon Tolkapon
Selegelin Pramipeksol, budesonid, formoterol, ketiapin fumarat, olanzapin, pioglitazon,
montelukast, Zoledromik Asit, valsartan, latanoprost, Irbesartan, Klopidogrel,
Atomoksetin, Deksamfetamin, Metilfenidat, Modafinil, Bleomisin, Daktinomisin,
Daunorubisin, Idarubisin, Mitomisin, Mitoksantron, Azasitidin, Kapesitabin, Kladribin,
Klofarabin, Sitarabin, Fludarabin, Flourourasil, Gemsitabin, merkaptopurin,
metotreksat, Nelarabin, Pemetreksed, Raltitreksed, Tiyoguanin. Apomorfin,
Betametazon, Kortizon, Deflazakort, Deksametozon, Hidrokortizon, Metilprednizolon,
Prednizolon, Triamsinolon, Siklosporin, Sirolimus, Takrolimus, Interferon Alfa,
Interferon Beta,
Özellikle tercih edilen bir düzenlemede aktif ajan, uykuyu sürdürememeyi tedavi etmek
üzere tasarlanir ve bu nedenle aktif ajan, zolpidem, zaleplon veya zopiklon gibi
yatistirici veya hipnotiktir.
kristalin-olmayan formlari, ayrica çesitli polimorflari içerir olarak anlasilir. Örnegin, aktif
ajan tek basina veya kombinasyon halinde bilesiklerin ve bunun farmasötik olarak
kabul edilebilir tuzlarinin tüm optik izomerlerini içerebilir treo izomerler “treo” olarak ve
kombine edilen eritro izomerler “eritro” olarak gösterilebilir.
Bulusa göre, bir kisi tarafindan alinmasi gereken ve kisi birinci olarak formülasyonu
aldiginda baslangiç olarak aktif ajani uygulamayan formülasyonlar saglanir. Ancak
daha sonraki bir zaman noktasinda ajan, ajanin bir “atimi” olarak denege uygulanir.
Uykuyu sürdürememenin tedavisiyle ilgili olarak kisi, bulusa göre olan ve uykuya sebep
olan/bunu sürdüren bir ajani içeren bir formülasyonu alir. Baslangiç olarak ajan,
formülasyondan salinmaz ancak belirli bir zaman periyodundan sonra, örnegin uykuyu
sürdürememekten muzdarip olan bir denegin uyanmasi beklendiginde ajan, denegi
tedavi etmek ve gece boyunca bunlarin uyanma ihtimalini azaltmak amaciyla bir
atimda salinir. Ajanin bu sekilde salinmasi istenir böylece denegin sabahlari uygun bir
zamanda uyanabilmesini ve uykuya sebep olan/bunu sürdüren ajanlarin yaygin bir yan
etkisi olarak uykulu hissetmemesini saglamak amaciyla ilaç denegin sisteminde uzun
bir zaman periyodu boyunca kalmaz.
L-HPC, LH-11'dir. LH-11 ve LH-21, belirli bir L-HPC türüdür ve Shin-Etsu Chemical
Co., Ltd., Tokyo, Japonya'dan elde edilebilir. L-HPC'Ier suda çözülmez ve
hidroksipropil gruplari ile minimal bir dereceye sübstitüe edilen bir glikoz omurgasi
içerir, LH-11 büyük oranda fibrözdür ve 55um bir ortalama partikül boyutuna sahiptir.
agirliga sahiptir. LH-21, orta derecede fibrözdür ve 45pm bir otalama partikül boyutuna
hidroksipropil içerigine sahiptir.
Mum balmumu, karnuba mumu, mikrokristalin mum, hidrojenize kastor yagi gibi uygun
herhangi bir mum olabilir. Özellikle tercih edilen bir mum gliseril behenat gibi bir gliseril
esterdir.
Burada yukarida açiklandigi üzere mevcut bulusun tercih edilen bir formülasyonunda
mum ve L-HPC, 40:60 ila 60:40 w/w'lik bir oranda mevcuttur. Daha çok tercih edildigi
varyasyonu ile, ilaç saliminda gecikmenin belirli bir uygulamaya yönelik uygun hale
getirilebilecegini anlayacaktir. Örnegin, bir mum olarak gliserol behenatin mevcut
bulusa göre gecikmeli bir salim katmani olarak kullanilan L-HPC olarak LH-11 ile 50:50
ww oraninin, yaklasik olarak 3 saatlik bir gecikmeli salim sagladigi gözlemlenir. Ancak,
L-HPC olarak LH-21 ile ayni oran salimda yalnizca 2 saatlik bir gecikme saglar. Ayni
zamanda L-HPC ile karsilastirildiginda mumun miktarinin azaltilmasinin, gecikmeyi
büyük oranda azalttigi gözlemlenir ve buna karsilik mumun miktarinin L-HPC oranina
arttirilmasi, salimin gecikmesinde önemli bir artisa neden olur. Dolayisiyla mumun L-
HPC'ye orani ve mum/L-HPC türünün uygun kontrolü ile, aktif ajan içeren bir çekirdegin
etrafini saran gecikmeli bir salim katmani içeren presIe-kaplanan bir tabletten aktif
ajanin salimindaki zaman gecikmesini kontrol etmek mümkündür.
Çekirdegi saran gecikmeli salim katmani ayrica çekirdegin içindeki aktif ajan ile ayni
veya farkli olabilen ve gecikmeli salim katmaninin çözünmesi/ayrilmasi sirasinda
salinmak üzere tasarlanan bir aktif ajan veya ajanlarin bir miktarini içerebilir.
Tedavi edilecek denek bir hayvan, örnegin bir memeli, özellikle bir insandir.
Uygulanacak aktif ajan miktari terapötik veya profilaktik olmaya yeterli olacaktir.
Terapötik veya pofilaktik ile istenen yaniti saglayabilen anlasilir ve tipik olarak bir tip
doktoru tarafindan karar verilir. Gereken miktar, en az ilgili aktif bilesik(ler), hasta,
tedavi edilmek veya önlenmek istenen durum ve formüsyondan bir veya daha fazlasina
bagli olacaktir. Ancak, bunun tedavi edilen hastanin vücut agirliginin kg basina
yaklasik 1 ug ila 1 g bilesik olmasi muhtemeldir.
Farkli dozlama rejimleri ayni sekilde, tipik olarak tip doktorunun yetkisinde
uygulanabilir. Bilesiklerin daha seyrek olarak, örnegin iki günde bir, haftalik veya iki
haftada bir uygulandigi rejimlerin, örnegin, ayrica mevcut bulus tarafindan
kapsanmasina ragmen, mevcut bulusun formülasyon en az günlük uygulama
saglayabilir.
Burada tedavi ile bir hastanin maruz kaldigi bir durumun en az bir iyilesmesi anlasilir;
tedavinin küratif olmasi (diger bir deyisle durumun giderilmesi ile sonuçlanmasi)
gerekmez. Benzer olarak burada önleme veya profilaksiye referanslar burada bir
durumun tam önlenmesini göstermez veya gerektirmez; bunun yerine göstergesi
mevcut bulusa göre profilaksi veya önleme vasitasiyla azaltilabilir veya geciktirilebilir.
Mevcut bulusa göre kullanima yönelik, burada açiklanan bilesikler veya bunun fizyolojik
olarak kabul edilebilir tuz, solvat, esteri veya diger fizyolojik olarak kabul edilebilir
fonksiyonel türevi, bunun bir veya daha fazla farmasötik olarak kabul edilebilir
eksipiyanlar veya istege bagli olarak diger terapötik ve/veya profilaktik içerik maddeleri
ile birlikte bilesik veya bunun fizyolojik olarak kabul edilebilir tuzu, esteri veya diger
fizyolojik olarak fonksiyonel türevini içeren presIe-kaplanan bir tablet formunda sunulur.
Herhangi bir eksipiyanin formülasyonun diger içerik maddeleri ile uyumlu olmasi ve
aliciya zararli olmamasi bakimindan kabul edilebilirdir.
Mevcut bulusun tabletleri teknikte halihazirda mevcut reaktifler ve teknikler ve/veya
burada açiklandigi üzere örnek niteligindeki yöntemler kullanilarak hazirlanabilir.
Tabletler oral, rektal veya vajinal uygulamaya yönelik olanlari içerir. Tabletleri, uygun
olmasi durumunda, uygun bir sekilde farkli dozaj ünitelerinde hazirlanabilir veya
eczacilik tekniginde iyi bilinen yöntemlerden herhangi biri araciligiyla hazirlanabilir.
Sikistirilmis tabletler, çekirdek tabletin uygun bir makinede, istege bagli olarak bir
baglayici, yaglayici, atil seyreltici, yaglayici ajan, yüzey aktif ajan veya dagitici ajan ile
karistirilan bir toz veya granüller gibi serbest akisli bir formda sikistirilmasiyla
hazirlanabilir. Çekirdek tablet akabinde gecikmeli salim katmaninin olusturulmasina
yönelik materyaller ile kaplanir. Tabletler istege bagli olarak örnegin diger bir enterik
kaplama araciligiyla kaplanabilir.
Rektal uygulamaya yönelik uygun tabletler en çok tercih edildigi üzere birim doz
supozituarlari olarak temsil edilir. Uygun tasiyicilar kakao yapi ve teknikte yaygin
olarak kullanilan diger materyalleri içerir. Supozituarlar uygun bir sekilde kaliplarda
sogutma ve sekillendirme akabinde yumusatilmis veya eritilmis tasiyici(lar) ile bir
tabletin karisimi araciligiyla olusturulabilir.
Mevcut bulusun tabletleri farmasötik prosesler kullanilarak diger bir deyisle dogrudan
sikistirma araciligiyla veya granülasyon isleme ve nihai tabletleme araciligiyla
hazirlanabilir. Proses, baslangiç olarak aktif ajani içeren bir çekirdegin olusturulmasi ve
akabinde çekirdegin gecikmeli salim katmani ile çevrelenmesi adimlarini içerebilir.
Çekirdek, bir veya daha fazla eksipiyan, örnegin bir selüloz eter, tipik olarak bir L-HPC
örnegin LH-21 ile bir veya daha fazla aktif ajanin dagitilmasiyla olusturulabilir.
Gecikmeli salim katmani, mum bileseninin eritilmesi ve akabinde L-HPC içeren diger
bilesenler ile karistirilmasiyla olusturulabilir. Karisim akabinde 500um -1 mm boyut
araligindaki granülleri elde etmek amaciyla ögütülmeden ve/veya bir elekteri
geçirilmeden önce sogutulabilir ve katilastirilabilir. Çekirdek akabinde dogrudan
sikistirma araciligiyla gecikmeli salim katmani materyali ile kaplanabilir. Tipik olarak
çekirdek gecikmeli salim materyalinin üst ve alt katmanlari arasinda sandviçlenir ve
böylece çekirdegin etrafini tamamen sarar.
Tabletlerin formülasyonuna yönelik tabletleme genellikle tabletlerin formasyonu veya
granülasyonuna yönelik kullanilan bir aparat kullanilarak gerçeklestirilebilir. Örnekler
tek-zimbali tabletleme makinesi, döner tabletleme makinesi ve tabletleme test cihazini
içerebilir.
basinç altinda gerçeklestirilir. 300 MPa'yi asan basinçlarda bozunmada bir gecikmeye
neden olabilirken, 50 MPa'dan az bir basinçta, ortaya çikan tablet, kolay bir sekilde
kullanimini rahatsiz eden yetersiz sertlige sahip olabilir.
Çekirdek ve/veya gecikmeli salim katmani, suda çözünmeyen bir dolgu maddesi, suda
çözünebilir dolgu maddesi veya bunlarin karisimlari gibi bir dolgu maddesini içerebilir.
Suda çözünmeyen dolgu, bir kalsiyum tuzu veya talk olabilir. Örnek niteligindeki suda
çözünen dolgular örnegin suda çözünen sekerler ve seker alkoller, tercihen Iaktoz,
glikoz, fruktoz, mannoz, galaktoz, karsilik gelen seker alkoller ve diger seker alkoller,
örnegin manitol, sorbitol veya ksilitoldur.
Gecikmeli salim katmanindaki dolgu maddesi, bulunmasi halinde çekirdek
bilesimindeki dolgu maddesi ile ayni veya bundan farkli olabilir. Pres kaplamali bilesim,
suda çözünmeyen bir dolgu maddesi içerebilirken örnegin çekirdek bilesimi, suda
çözünebilir bir dolgu maddesini içerebilir.
Çekirdek ve/veya gecikmeli salim katmaninin içinde yaglayicilari (örnegin talk ve
magnezyum stearat), glidantlar (örnegin isli veya koloidal silika), pH düzenleyiciler
(örnegin asitler, bazlar ve tampon sistemler) ve farmasötik olarak faydali isleme
yardimcilari dahil olmak üzere diger eksipiyanlar mevcut olabilir. Bu tür diger
eksipiyanlarin olmasi halinde, çekirdek veya gecikmeli salim katmaninda ayni veya
farkli olabilecegi anlasilacaktir.
Bulusun tercih edilen bir düzenlemesinde, çekirdek bilesenleri (aktif ajan ve istege bagli
eksipiyan) birlikte karistirilir ve uygun çekirdeklere sikistirilir. Karistirma herhangi bir
ekleme sirasinda gerçeklesebilir. Tercihen çekirdekler en küçük hacimli bilesen ile
baslanmasi ve akabinde büyük hacimli bilesenlerin sirayla eklenmesi araciligiyla
karistirilir.
Tablet ayrica istege bagli ilave kaplamalar ile kaplanabilir. Ilave kaplamalar, pH'ye
bagimli veya pH'den bagimsiz, estetik veya islevsel olabilir; burada kaplama, bir
enterik kaplama (midede salimi önlemesi amaçlanan) olabilir, burada tanimlandigi
üzere gecikmeli salima yönelik 'saat' veya süre, mide bosalmasi meydana gelene ve
enterik kaplamanin çözünmesi gerçeklesene (örnegin Sintigrafi çalismalari kullanilarak
belirlenebilecegi gibi) kadar baslamayacaktir. Enterik kaplamanin zaman geciktirme
katmanindan gecikme ile birlikte çözünmesine yönelik alinan süre, bagirsagin alt
kademelerinde, özellikle distal ileum ve/veya kolonda ilaç salimini saglayacaktir. Bu tür
ilave kaplamalar tercihen film olusturma materyallerini içerir. Ayrica uyuma konusunda
zorluk çeken deneklere yönelik gecikmeli salim katmani ve/veya ilave katman, hizli
salima yönelik bir uykuya sebep olan ajani içerebilir.
Detayli Açiklama
Mevcut bulus bu noktada örnek yoluyla ve sekillere referans ile ayrica açiklanacaktir,
Sekil 1, gecikmeli bir salim katmaninda bir 50/50 ww oraninda gliserol behenat
ve LH-11 içeren bir tabletten bir ilacin salim profilini gösterir;
Sekil 2, gecikmeli bir salim katmaninda bir 50/50 ww oraninda gliserol behenat
ve LH-21 içeren birtabletten bir ilacin salim profilini gösterir;
Sekil 3 ve 4, gecikmeli bir salim katmaninda 30:70 ww oraninda gliserol
behenat ve LH-11 (sekil 3) ve LH-21 (sekil 4) içeren bir tabletten bir ilacin salim
profilini gösterir;
Sekil 5, Zolpidemin gecikmeli salim formülasyonunun salimini gösteren Gama
Sintigrafi Görüntülerini gösterir;
Sekil 6, 6 denekte plazma içindeki ilaç seviyelerinin Farmakokinetik analizini
gösterir; ve
Sekil 7, 50/50 w/w gliserol behenat/LH32'nin bir gecikmeli salim katmanini
içeren bir tabletin salim profilini gösterir.
Uyumavi sgrdürememenin tecßvi edilmesine vönelik formülasyon
1. Klinik ihtiyaç
Bu formülasyon profili, baslangiçta uykuya dalan akabinde yeniden uyana ve 2-3 saat
sonra uyuyamayan insanlara yönelik bir tedavi olarak tasarlanmistir.
2. Yöntemler
2.1. çekirdek tablet Karisimi ve Çekirdek Tablet Kompresyonu
Magnezyum stearat haricinde yukaridaki unsurlarin toz karisimi, turbula
karistirici içinde 10 dakika boyunca, akabinde magnezyum stearat eklenmistir
ve tamami 5 dakika daha karistirilmistir.
(ii) 90mg çekirdek ucu, 10 saniye boyunca 1 tonda bir 6.9 mm kalip/Zimba
takiminda harmanlanarak sikistirilmistir.
(iii) Tabletler kullanima kadar amber cam sise içinde saklanir.
2.2. Granüller (çekirdek katmanin etrafini sarmak üzere)
(i) Gliserol behenat (GB) ve LH-11, Tablo 1`e göre darasi alinmis tarti kaplarinda
tartilmistir.
Eksipiyan Agirlik (9)
(ii) GB 100°C'de sicak bir plaka seti üzerinde cam bir beher içine yerlestirilmistir.
GBlnin erimesinin akabinde, üniform bir karisim elde edilene kadar karistirilirken
kademeli olarak LH-11 eklenmistir.
(iii) karisim oda sicakligina soguyana kadar sürekli olarak karistirilmistir. Granüller
sonraki adim öncesinde oda sicakliginda en az 30 dakika boyunca birakilir.
(iv) Sogutulmus granüller 1 mm'lik bir elekten geçirilmistir (bir spatula ve bir firça
kullanilarak) ve 500 umtlik bir elek üzerinde toplanmistir bu sekilde kullanilan granüller
500 um - 1 mm'lik boyut araligindadir. (v) Granüller kullanilana kadar amber vida-
kapakli cam kavanozda saklanmistir.
2.3. Formülasyon Kompresyonu
(i) Bir 13 mm kalip ve eslesen düz yüzeyli zimbalar, formülasyonu sikistirmak
üzere kullanilmistir. 6 tablet için, 12 x 250 mg granüller (çekirdek katmanin
etrafini sarmak üzere) darasi alinmis tartim kaplarinda tartilmistir.
(ii) 250 mg granül, alt zimbanin üstüne yerlestirilmistir, çekirdek tablet üzerine
damlatilmistir ve tepe kisminin üzerinde diger 250 mg granülün
yerlestirilmesinden önce merkezilestirilmistir (merkezilestirme aleti).
(iii) Formülasyon, bir 13 mm kalip/Zimba takiminda 2 dakika boyunca 5 tonda
sikistirilmistir.
2.4. Çözünme
M, pH7'de) gerçeklestirilmistir.
3. Sonuçlar (50:50, GB:LH-11)
Sekil 1'den görülebilecegi üzere yaklasik olarak 3 saatlik bir gecikme akabinde ilacin
hizli bir atimli salimi gözlemlenir.
4. Destekleyen Veriler
Sekil 2`de görülebilecegi üzere, LH-21'ye yönelik LH-11'in sübstitüe edilmesi, salim
süresinin gecikmesinde bir azalmaya sebep olur. Bu tür bir azalma, bütün öngörülen
uygulamalara yönelik istenilir olmayabilir.
4.2. 80:20, GB:LH-11
12 saat üzerinde zolpiden çekirdek tabletin sifir salimi, veriler gösterilmez.
4.3. 80:20, GB:LH-21
12 saat üzerinde zolpiden çekirdek tabletin sifir salimi, veriler gösterilmez.
4.4. 30:70, GB:LH-11
Sekil 3'te görülebilecegi üzere, gliserol behenatin LH-11 oranina azaltilmasi, salim
süresinin gecikmesinde önemli bir azalmaya sebep olur.
4.5. 30:70, GB:LH-21
Sekil 4'te görülebilecegi üzere, gliserol behenatin LH-21 oranina azaltilmasi, salim
süresinin gecikmesinde önemli bir azalmaya sebep olur.
LH-11'in yerinde dis granüllerde LH-21'in kullanilmasi, yukarida gösterilen her iki
örnekte de çekirdek tableti yaklasik olarak 30 dakika erken salar.
Ekstraksiyon Yöntemi I Zolpidemin Plazma seviyelerinin analizi
Mategaller
Insan plazmasi, Iityum heparin, kaynak ABD : Sera Iaboratories international Ltd, Bx
H911239 Zolpidem tartrat
DEE: Fisher laboratuari reaktif kalitesi Bx 1097413
NaOH: Q3 su kullanilarak hazirlanmistir ve NaOH: Sigma Aldrich, reaktif kalitesinde
boncukar, %97 Bx 012098H
Yöntem
vorteks bos plazma
4OOUl bos plazma, cam vidali kapakli tüplerin içine eklenir
Kalibrasyon
Bos hazirlanis - standaitlardan önce hazirlanmak üzere
100UI mobil fazin 400uI bos plazmaya eklenmesi
vorteks 10 saniye
50u| 1M NaOH'un eklenmesi
vorteks 10 saniye
4mL DEE'nin eklenmesi ve vorteks 3 dakika (dikkat: DEE, her gün taze olarak siseden
bosaltilir)
Mobil faz/DEE'nin her eklenmesinden sonra pipet uçlari degistirilir
Standart hazirlama
En düsük konsantrasyon standardi, vorteks standardi ile baslanmasi
100UI standartin 400ul bos plazmaya eklenmesi
Vorteks 10 saniye
50ul 1M NaOH'un eklenmesi
Vorteks 10 saniye
4mL DEE'nin eklenmesi ve vorteks 3 dakika (dikkat: DEE, her gün taze olarak siseden
bosaltilir)
Standart/DEEnin her eklenmesinden sonra pipet uçlari degistirilir
Numunelerin 2000rpm'de 3 dakika santrifüjlenmesi
Cam pipetler kullanilarak vidali üst kismi olan temiz etiketli cam tüpün içinde üst
katmanin çikartilmasi
40°C'de nitrojen altinda kuruyana kadar buharlastirilmasi (ayni zamanda
buharlastirmak üzere RVC'nin kullanilmasi, 40°C,
100mbar, 25mis)
1OOUI mobil faz içinde yeniden olusturulmasi. 30 dakika boyunca durmasina izin
verilmesi ve akabinde 3 dakika boyunca vorteks
Eklenti ile HPLC viyaline aktarilmasi
Numune hazirlanisi
Karistirilmak üzere vorteks numuneleri
500UI numunenin Vidali kapakli cam tüpe eklenmesi
50ul 1M NaOH'un eklenmesi
Vorteks 10 saniye
4mL DEE'nin eklenmesi ve vorteks 3 dakika (dikkat: DEE, her gün taze olarak siseden
bosaltilir)
Standart/DEEnin her eklenmesinden sonra pipet uçlari degistirilir
2000rpm'de 3 dakika boyunca numunelerin santrifüjlenmesi
Cam pipetler kullanilarak Vidali üst kismi olan temiz etiketli cam tüpün içinde üst
katmanin çikartilmasi
40°C`de nitrojen altinda kuruyana kadar buharlastirilmasi (ayni zamanda
buharlastirmak üzere RVC'nin kullanilmasi, 40°C.
100mbar, 25mins
1OOUI mobil faz içinde yeniden olusturulmasi. 30 dakika boyunca durmasina izin
verilmesi ve akabinde 3 dakika boyunca vorteks
Eklenti ile HPLC viyaline aktarilmasi
Mobil Faz Hazirlanisi
Materyaller
Potasyum fosfat monobazik, SAFC lot 1370660
NaOH: Sigma Aldrich, reaktif kalitesinde boncukar, %97 Bx 01209BH
Asetonitril: Fisher HPLC gradeBX 1095614
20mM potasyum fosfat tamponu, Q3 su ile hazirlanir, pH NaOH ile 6'ya ayarlanir
Buchner, 0.2um 47mm naylon membran ile filtrelenir
Kroma tografik Kosullar
Perkin Elmer LS 40 floresans detektörü ile Gynkotek HPLA sistemi
mikron
Saptama: eksitasyon: 251 nm emisyon:289
Gradyan: baslama kosullari %60 tampon %40 asetonitril akis hizi 1mL/dakika
dakika üzerinde %40-80 asetonitril artisi, 4 dakika boyunca %80'de tutulur
Bir sonraki enjeksiyondan önce 2 dakika boyunca baslama kosullarina geri dönülür
Enjeksiyon hacmi 20uL
Eklenen Standart Aralik
1 - 150nglmL plazma
Klinik Deney Protokolü - Zolpidem 10 mg gecikmeli salim (2 saat süreli gecikme) Klinik
çalismalar, olan 18-65
arasinda bir yasta olan Saglikli erkek gönüllülerde gerçeklestirilmistir. Gecikmeli salim
tabletlerinin gastrointestinal geçisi gastrointestinal sistemden absorpisyonu önleyen,
dietilentriaminpentaasetik asit (DTPA) ile kompleks hale getirilen bir radyo göstergesi,
teknesyum-99m (99mTc) eklenmesi araciligiyla karakterize edilmistir. Radyo etiket
çekirdek katmana eklenir. Her bir tablet 4 MBq 99mTc-DTPA ile radyo etiketlenir ve
uyku vaktinde 240 ml su ile uygulanir.
Deneklere, dozajlamadan 4 saat önce salata ile kizarmis tavuk, az yagli yogurt ve bir
bardak kafeinsiz çay, kahve veya meyve suyunu içeren standart bir aksam yemegi
verilmistir.
Sintigrafik görüntüleme düsük-enerjili yüksek-çözünürlüklü bir kolimatör ile donatilan bir
Siemens E-Cam gama kamera kullanilarak gerçeklestirilmistir. Deneklerin yatarken
görüntülendigi uyku zamanlari haricinde denekler ayakta bir pozisyonda
görüntülenmistir.
Asagidaki görüntüleme çizelgesi kullanilmistir:
Her bir 25 saniyelik sürede bir önceki statik edinimler, radyoaktif isaretleyicinin
tam salimina kadar dOZIamadan hemen sonra her 15 dakikada bir toplanmistir.
lelik bir doz-öncesi kari numunesi dozlamadan 15 dakika önce her denekten
alinmistir. Asagidaki dozajlama kan numuneleri, asagidaki çizelgeye göre alinmistir.
Sintigrafi ile ani salim gözlemlenene kadar her 15 dakikada bir akabinde 2 saat
boyunca her 15 dakikada bir akabinde 1 saat boyunca her 30 dakikada bir akabinde
çalisma gününün sonuna (dozdan sonra 9 saat) kadar saat basi. Bakiniz sekil 5.
Kan numuneleri 10 dakika boyunca 2000 g'de santrifüjlenmistir ve plazma fraksiyonu
çikartilmistir ve akabindeki analiz için -20 °C'de saklanmistir. Bakiniz Sekil 6.
Sekil 7, atimli ilaç saliminin öncesinde gecikme periyodunu degistirme yetenegini
gösteren 50/50 w/w gliserol behenat/LH32'nin bir gecikmeli salim katmanini içeren bir
tablet formülasyonunun salim profilini gösterir.
Zolpidem salimi (%)
Sure (dakika)
Zolpidem salimi (3/0)
E30-l
I--i'v--Ii-Tii--i'v-'v-'rv
Sure (dakika)
Sure (dakika)
Zolpidem salimi ('70)
Süre (dakika)
-100 0 200
135 dakika 185 dakika
tanidim nun& plazma
Zolpldem PK
-o-Dcnek
Diklofenak Salimi (1%)
300 400
Sure (dakika)
Claims (2)
- ISTEMLER . Aktif bir ajanin gecikmeli akabinde atimli bir salimina yönelik presle kaplanan bir tablet formülasyonu olup, özelligi tabletin asagidaki unsurlari içermesidir bir eksipiyan(lar) ile birlikte aktif ajanlari içeren bir çekirdek; ve çekirdegin etrafini saran ve 40:60 ila 60:40 w/w”lik bir oranda bir mum ve büyük oranda fibröz olan ve yaklasik 55iJm bir moleküler agirliga sahip olan düsük Sübstitüeli hidroksipropil selüloz (L-HPC) içeren bir gecikmeli salim katmani; burada gecikmeli salim katmani bir denek tarafindan tabletin uygulanmasindan sonra 1.5 - 8 saat boyunca çekirdek içindeki aktif ajanin salimini geciktirir ve bundan sonra aktif ajanin çekirdekten atimli bir salimi meydana gelir, böylece çekirdekteki aktif ajanin en az
- 2. Önceki istemlerden herhangi birine göre presIe-kaplanan tablet olup, özelligi asagidaki aktif ajanlardan bir veya daha fazlasini içermesidir: Gastro Ilaçlar Antasitler - alüminyum hidroksit, magnezyum karbonat. magnezyum trisilikat, hidrotalsit, simettikon alginatlari, Antispazmodikler - atropin sülfat, disikloverin hidroklorid, hiyosin bütilbromin, propantelin bromür, alverin sitrat, mebeverin hidroklorid, Motilite uyaricilar - metoklorpramid, domperidon H2 - Reseptör antogonistleri - Simetidin, famotidinnizatidin, ranitidin Selatlar - Tripotasyum disitratbismutat, sukralfat, Prostaglandin analoglari - misoprostol Aminosalisilatlar - balsazid sodyum, mesalazin, olsalazin, sülfasalazin Kortikosteroidler - beklometazon dipropinat, budenosid, hidrokortizon, pednisolon Immün yaniti etkileyenler - siklosporin, merkaptopürin, metotreksat, adalimumab, infliksimab Uyarici Laksatifler - bisakodil, dantron, dokusat, sodyum pikosülfat, Biliyer bilesim ve akisi etkileyen ilaçlar - ursodeoksikolik asit Safra asiti sekestranlari - kolestiramin, Oksifensiklimin, Kamilofin, Mebeverin, Trimebütin, Rosiverin, Disikloverin, Diheksiverin, Difemerin, Piperidolat Benzilon, Mepenzolat, Pipenzolat, Glikopironyum, Oksifenonyum, Fentienat, Mentantelin, Propantelin, Otilonyum bromür, Tridiheksetil, Izopropamid, Heksosikliyum, Poldin, Bevonyum, Difemanil, Tiemonyum iyodür, Prifinyum bromür, Timepidyum bromür, Fenpiverinyum Papaverin, Drotaverin, Moksaverin 5-HT3 antagonistleri (örnegin Alosetron, Silansetron), 5-HT4 agonistleri (Örnegin Mosaprid, Prukaloprid, Tegaserod) Fenpipran, Diizopromin, Klorbenzoksamin, Pinaveryum, Fenoverin, ldanpramin, Proksazol, Alverin, Trepibuton, Izometepten, Karoverin, Floroglusinol, Silikonar, Trimetildifenilpropilamin Atropin, Hiyosiyamin Skopolamin (örnegin, Bütilskopolamin, Metilskopolamin), Metilatropin, Fentonyum, Simetropyum bromür primer dopamin antagonistleri, örnegin Metoklopramid/Bromoprid, Kleboprid, Domperidon ve Alizaprid, 5-HT4 agonistleri, örnegin Sinitaprid ve Sisaprid, Proton pompasi inhibitörleri Omeprazol, Iansoprazol, pantoprazoli esomeprazol, rabeprazole sodyum, opioidler ve opioid reseptörü antagonistleri, örnegin kodein, morfin, loperamid, difenoksilat, metilnaltrekson bromür Analjezik Asetaminofen Diklofenak Diflunisal Etodolak Fenoprofen Flurbiprofen Ibuprofen Indometasin Ketoprofen Ketorolak Meklofenamat Mefenamik Asit Meloksikam Nabumeton Naproksen Oksaprozin Fenilbütazon Piroksikam Sulindak Tolmetin Selekoksib Buprenorfin Butorfanol Kodein, Hidrokodon Hidromorfon Levorfanol Meperidin Metadon, Morfin, Nalbufin Oksikodon Oksimorfon Pentazosin, Propoksifen, Tramadol, kodein Uyku ilaçlari Hipnotikler - Nitrazepam, Flurazepam, Loprazolam, Lormetazepam, Temazepam, Zaleplon, Zolpidem, Zopiklon, Kloral Hidrat, Triklofos, Klometiazol, Kuazepam, triazolam Estazolam Klonazepam Alprazolam, Eszopiklon, Rozerem, Trazodon, Amitriptilin Doksepin, Benzodiazepin ilaçlar, melatonin, difenhidramin ve Kedi otu gibi bitkisel ilaçlar Kardio vasküler ilaçlar Cardiak glikosidler - Digoksin, digitoksin, Fosfodiesteraz inhibitörleri - enoksimon, milrinon Tiazidler ve ilgili diüretikler -bendroflumetiazid, klortalidoni siklopentiazid, inapamid, metolazon, ksipamid Diüretikler - furosemid, bumetanid, torasemid, Potasyum koruyucu diüretikler ve aldosteron antagonistleri - amilorid hidroklorid, triamteren. weplerenon, spironolakton, Osmotik diüretikler- manitol Arimiye yönelik ilaçlar - adenosin, amiodaron hidroklorid, disopiramid, flekainid asetat, propafenon hidroklorid, Iidokain hidroklorid, Beta adrenoreseptör engelleyici ilaçlar - propanalol, atenolol, asebütolol, bisoprolol, fumarat, karvedilol, seliprolol, esmolol, Iebatolol, metoprolol tartrat, nadolol, nebivolol, oksprenolol, pindolol, solatol, timolol, Hipertansiyon -ambrisentan, bosentan, diazoksid, hidralazin, iloprost, minoksidil, sildenafil, sitaksentan, sodyum nitroprussid, klonidin, metildopa, moksonidin, guanetidin monosülfat, doksazosin, indoramin, prazosin, terazosin, fenoksibenzamin, fentolamin mesilat, Renin-anjiyotensin sistemi etkileyen ilaçlar - Kaptropril, Silazapril, Enalapril Maleat, Fosinopril, Imidapril, Lisinopril, Moeksipril, Perindopril Erbumin, Kinapril, Ramipril, Trandolapril, Kandesartan Sileksetil, Eprosartan, Irbesartan, Losartan, Olmesartan Medoksomil, Telmisartan, Valsartan, Aliskiren. Nitratlar, kalsiyum kanal Blokerleri ve antianjinal ilaçlar - Gliseril trinitrat, Izosorbid Dinitrat, Izosorbid Mononitrat, Amlodipin, Diltiazem, Felodipin, Isradipin, Lasidipin, Lerkanidipin, Nikardipin, Nifedipin, Nimodipin, Verapamil, Ivabradin, Nikorandil, Ranolazin, Periferik Vazodilatörler ve iliskili ilaçlar - Silostazol, Inositol Nikotinat, Moksisilit, Naftidrofuril Oksalat, Pentoksifyilin, Sempatomimetikler - Dopamin, Dopeksamin, Efedrin, Metaraminol, Noradrenalin Asit Tartrat, Norefidrin Bitartrat, Fenilefidrin, Antikoagülanlar ve Protamin -Heparin, Bemiparin, Dalteparin. Enoksaparin, Tinzaparin, Danaparoid, Bivalirudin, Lepirudin, Epoprostenol. Fondaprinuks, Varfarin, Asenokoumarol, Fenindion, Dabigatran Eteksilat, Rivaroksaban, Protamin Sülfat, Antiplatelet Ilaçlari -Absiksimab, Asprin, Klopidogrel, Dipiridamol, Eptifibatid, Prasugrel, Tirofiban, Fibrinolitik ve antifibrinolitik Ilaçlar -Alteplaz, Reteplaz, Streptokinaz, Tenekteplaz, Ürokinaz, Etamsilat, Traneksamik Asit, Lipid Düzenleyici Ilaçlar -Atorvastatin, Fluvastatin, Pravastatin, Rosuvastatin, Simvastatin, Kolesevam, Kolestiramin, Kolestipol, Ezetimib, Bezafibrat, Siprofibrat, Fenofibrat, Gemfibrozil, Asipmoks, Niktotinik Asit, Omega üç yag asiti bilesikleri, Etanolamin Oleat, Sodyum Tetradesil Sülfat. CNS Ilaçlari - Benperidol, Klorpromazin, Flupentiksol, Haloperidol, Levomepromazin, Perisiazin, Perfenazin, Pimozid, Proklorperazin, Promazin, Sülpirid, Trifluoperazin, Zuklopentiksol, Amisülprid, Aripiprazol, Klozapin, Olanzapin, Paliperidon, Ketiapin, Riperidon, Sertindol, Zotepin, Flupentiksol, Flufenazin, Olanzapin Embonat, Pipotiazin Palmitat, Risperidon, Zuklopentiksol Dekanoat, Karbamazepin, Valproat, Valproik asit, Lityum Karbonat, Lityum Sitrat, Amitriptilin, KIOmipramin, Dosulepin, Imipramin, Lofepramin, Nortriptilin, Trimipramin, mianserin, Trazodon, Fenelzin, Izokarboksazid, Tranilsipromin, Moklobemid, Sitalopram, Essitalopram, Fluoksetin, Fluvoksamin, Paroksetin, Sertralin, Agomelatin, Duloksetin, Flupentiksol, Mirtazapin, Reboksetin, Tritofan, Venflaksin, Atomoksetin, Deksametamin, Metilfenidat, Modafinil, Eslikarbazepin, Okarbazepen, Etosüksimid, Gabapentin, Pregabalin, Lakosamid, Lamotrigin, Levetirasetam, Fenobarbital, Primidon, Fenitoin, Rufinamid, Tiagabin, Topiramat, Vigabatrin, Zonisamie, ropinirol, Rotigotin, Ko-Beneldopa, Levodopa, Ko-Kareldopa, Rasagilin, Selegilin, Entakapon, Tolkapon, Amantidin, Orfenadrin, Prosiklidin, Trihesifenidil, Haloperidol, Pirasetam, Riluzol, Tetrabenazin, Akamprosat, Disülfiram, Bupropiyon, Varenisilin, Buprenorfin, Lofeksidin, Donepezil, Galantamin, Memantin, Rivastigimin. Anti-Enfektivler- Benzilpenisilin, Fenoksimetilpenisilin, Flukloksasilin, Temosilin, Amoksisilin, Ampisilin, Ko-Amoksiklav, Ko-Fluampisil, Piperasilin, Tikarsilin, Pivmesilinam, Sefalosporinler, Sefaklor, Sefadroksil, Sefaleksin, Sefiksim, Sefotaksim, Sefradin, Seftazidim, Sefuroksim, Ertapenem, Imipenem, Meropenem, Aztreonam, Tetrasiklin, Demeklosiklin, Doksosiklin. Limesiklin, Minosiklin, Oskitetrasiklin, Tigesiklin, Gentamisin, Amikasin. Neomisin, Tobramisin, Eritromisin, Azitromisin, Klaritromisin, Telitromisin, Klindamisin, Kloramfenikol, Fusidik Asit, Vankomisin, Teikoplanin, Daptomisin, Linezolid, Kinupristin, Kolistin, Ko-Trimoksazol, Sülpadiazin, Trimetoprim Kapreomisin, Sikloserin, Etambütol, Izoniazid, Pirazinamid, Rifabutin, Rifampisin, Streptomisin, Dapson, Klofazimin, Metronidazol, Tinidazol, Siproflaksasin, Levoflaksasin, Moksifloksasin, Nalidiksik Asit, Norflaksin, Orflaksasin, Nitrofurantoin, Metenamin Hippürat, Amfoterisin, Anidulafungin. Kaspofungin, Flukonazol, Flusitosin, Griseofluvin, Itrakonzol, Ketokonazol, Mikafungin, Nistatin, Posakonazol, Terbinafin, Vorikonazol, Abakavir, Didanosin, Emtrisitabin, Lamivudin, Stavudin, Tenofovir Disoproksil, Zidovudin, Atazanavir, Darunavir, Fosamprenavir, Indinavir, Lopinair, Nelfinavir, Ritonavir, Sakinavir, Tipranavir, Efavirenz, Etravirin, Nevarapin, Enfuvirtid, Maravirok, Raltegravir, Asiklovir, Famsiklovir, Inosin Pranobeks, Valasiklovir, Sidofovir, Gangsiklovir, Foskarnet, Valgangsiklovir, Adefovir Dipivoksil, Entekavir, Telbivudin, Amantadin, Oseltamivir, Zanamivir, Palivizumab, Ribavirin, Artemeter, Klorokin, Meflokin Primakin, Proguanil, Pirimetamin, Kinin, Doksisiklin, Diloksanid Furoat, Metronidaziol, Tinidazol, Mepakrin Sodyum Stiboglukonat, Atovakuon, Pentamidin Izetionat, Mebendazol, Piperazin, Digerleri: Benztropiprosiklidin biperiden, Amantadin Bromokriptin Pergolid Entakapon Tolkapon Selegelin Pramipeksol, budesonid, formoterol, ketiapin fumarat, olanzapin, pioglitazon, montelukast, Zoledromik Asit, valsartan, Modafinil, Bleomisin, Daktinomisin, Daunorubisin, Idarubisin, Mitomisin, Mitoksantron, Azasitidin, Kapesitabin, Kladribin, Klofarabin, Sitarabin, Fludarabin, Flourourasil, Gemsitabin, merkaptopurin, metotreksat, Nelarabin, Pemetreksed. Raltitreksed, Tiyoguanin, Apomorfin, Betametazon, Kortizon, Deflazakort, Deksametozon, Hidrokortizon, Metilprednizolon, Prednizolon, Triamsinolon, Siklosporin, Sirolimus, Takrolimus, Interferon Alfa, Interferon Asagidaki hastalik veya durumlardan bir veya daha fazlasini tedavi etmenin bir yönteminde kullanilmaya yönelik istem ?ye göre presIe-kaplanan tablettir: Merkezi Sinir Sistemi hastaliklari, örnegin Nörojenik agri, felç, demans, Alzheimer hastaligi, Parkinson hastaligi, nöronal dejenerasyon, menejit, spinal kord hasari, serebral vazospazm, amiyotrofik lateral skleroz Kardiovasküler hastalik, hipertansiyon, ateroskleroz, anjin, arteriyel obstrüksiyon, periferik arter hastaligi, miyokardiyal patoloji, Aritmi, Akut Miyokard Enfakrtüs, Anjin, Kardiyomiyopati, Konjestif kalp yetmezligi, Koroner arter hastaligi (CAD), Karotis arter hastaligi, Endokardit, Hiperkolesterolemi, hiperlipidemi, Periferik arter hastaligi (PAD) Genitoüriner Rahatsizliklar; erektil disfonksiyon, üreriner organ hastaliklari benign prostat hipertrofisi (BPH), Renal tübüler asidoz, diyabetik nefropati, glomerülonefrit, glomerüloskleroz, üriner sistem enfeksiyonu, fekal inkontinans Göz hastaliklari glakom, blefarit, oküler hipertansiyon, retinopati, konjonktivit, sklerit, retinit, keratit, kornea ülseri, iritis, korioretinal inflamasyon, makuler ödem, Kseroftalmi Pulmoner hastalik astim, pulmoner hipertansiyon, akut solunum sikintisi sendromu, COPD, amfizem, pnömoni, tüberküloz, bronsit, Akut Bronsit, Bronsektazi, Bronsiyolit, Bronkopulmoner displazi, Bisinoz, Koksidioidomikoz (Koksi), Kistik Fibroz, Grip, Akciger Kanseri, Mezotelyoma Metabolik hastaliklari; Hiperkalsiüri, Hiperglisemi, Hiperinsülinemik hipoglisemi, Hiperinsülinizm, Hiperüsinüri, Hipoglisemi Eksokrin ve Endokrin; Addison hastaligi, Hipoaldosteronizm, cushing sendromu, diyabet, Guatr, Hipertiroidzm, Hipotiroidzm, Tiroidit, pankreatit Hepatik bozukluklar, Hepatit, Alkolik-olmayan yagli karaciger hastaligi, siroz, hepatik kanser, Primer sklerozan kolanjit, primer biliyer siroz, Budd-Chiari sendromu, Otoimmün ve Inflamatuar hastaliklar, multipl Skleroz, romatoid artrit, psöriyazis, diyabet, sarkoidoz, Addison Hastaligi, Saçkiran, Amyotrofik Lateral Skleroz, Ankilozan Spondilit, poliartiküler Artrit, Atopik alerji, topik Dermatit, Otoimmün hepatit, Çölyak hastaligi, Sagaz hastaligi, Çölyak hastaligi, Cogan sendromu, Chron Hastaligi, Cushing Sendormu, Diyabet tip 1, Endometriyoz, Eozinofilik fasitt, Fibromiyalji/Fibromiyozit, Gastrit, Glomerülonefrit, Graves hastaligi Guillain-Barre' sendromu (GBS), Hashimoto ensefalit, Hashimoto tiroiditi, Hemolitik anemi, Idiyopatik Inflamatuar Demiyelinizan Hastaliklar, Idiyopatik pulmonerfibroz, interstisyel sistit, Juvenil idiyopatik artrit, Juvenil romatoid artrit, Kawasaki Hastaligi, Iiken sklerozus, Lupus eritematozus, Méniere hastaligi, Miyastenya gravis, miyozit, Narkolepsi, Pernisiyöz anemi, perivenöz ensefalomiyelit, Polimiyaljiya romatika, Primer biliyer siroz, Psoriatik artrit, Reiter sendromu, Romatoid ates, Sarkoidoz, Sizofreni, Sjögren sendormu, Spondiloartropati, Ülseratif kolit Musculoskeletal bozukluklar: osteoartrit, orteoporoz, Osteonekroz, Artrit, Paget Hastaligi, Bursit, Kostokondrit, Tendonit Cilt bozukluklari; Akne, alopesi, andidiyaz, selülit, dermatit, egzema, epidermolizis bülloza, eritrazma, uçuk, erisipel, Folikülit, impetigo, mantar hastaligi, skabiyez, Tinea, Trikomikoz ENT bozukluklari; Otit, sinüzit, Iarinjit, faranjit, Iarinjit, meniere hastaligi, Digerleri: akut ve kronik agri, viral enfeksiyon, kanser, mastoidit, mirinjit, otitis media, rinit, sinüzit, Sialadenit, Retrofarengeal apse, Tonsilofarenjit, Gastro- intestinal bozukluklar Irritabl bagirsak sendromu, nekrotizan enterokolit ülser-olmayan dispepsi, kronik intestinal psödo-obstrüksiyon, fonksiyonel dispepsi, kolonik psödo- obstrüksiyonduedenogastrik reflü, gastroözofajeal reflü hastaligi, ileus inflamasyonu, gastroparezi, mide yanmasi, kabizlik - (örnegin opoidler gibi ilaçlara yönelik kullanim ile iliskili kabizlik), kolorektal kanser, kolonik polipler, divertikülit, kolorektal kanser, Barrett Özefagusu, Sindirim Sisteminde Kanama, Çölyak Hastaligi, Kolon Polipleri, Kabizlik, Crohn Hastaligi, Siklik Kusma Sendromu, Gecikmeli Mide Bosalmasi (Gastroparezi), Diare, Divertikülozis, Duodenal Ülserler, Feçes Inkontinansi, Safra tasi, Sindirim Sisteminde Gaz, Gastrit, Gastroözofajeal Reflü Hastaligi, Mide yanmasi, Hiyatus Hernisi, Hemokromatoz, Hemoroid, Hiyatus Hernisi, Hirschsprung Hastaligi, Hazimsizlik, Inguinal Herni, Laktoz Intoleransi, Peptik Ülserler, Polipler, Porfiri, Primer Biliyer Siroz, Primer Sklerozan Kolanjit, Proktit, Hizli mide Bosalmasi, Kisa Bagirsak Sendromu, Mide Ülserleri, ülseratif Kolit, Ülserler, Whipples Hastaligi. istem 1'e göre presle kaplanan bir tablet olup, özelligi aktif ajanin uykuyu sürdürememeyi tedavi etmek üzere tasarlanmasi, istege bagli olarak zolpidem, zaleplon veya zopiklon gibi bir yatistirici veya hipnotik olmasidir. Önceki herhangi bir isteme göre tablet olup, özelligi mumun balmumu, karnuba mumu, mikrokristalin mum, hidrojenize kastor yagi veya bir gliseril ester olmasidir. istem 5'e göre tablet olup, özelligi gliseril esterin gliserol behenat olmasidir. . Önceki herhangi bir isteme göre tablet olup, özelligi mum ve L-HPC'nin 45:55 ila 55:45 w/w bir oranda mevcut olmasidir. . Önceki herhangi bir isteme göre tablet olup, özelligi ayrica ilave bir kaplamayi içermesidir, burada kaplama pH'ye bagimli, pH'den bagimsiz, estetik veya islevseldir. . Önceki herhangi bir isteme göre presle kaplanan tablet olup, özelligi aktif ajanin yatistirici veya hipnotik bir ajan olmasidir.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB1003766.1A GB201003766D0 (en) | 2010-03-05 | 2010-03-05 | Pulsatile drug release |
Publications (1)
Publication Number | Publication Date |
---|---|
TR201802596T4 true TR201802596T4 (tr) | 2018-03-21 |
Family
ID=42136598
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TR2018/02596T TR201802596T4 (tr) | 2010-03-05 | 2011-03-04 | Pulsatil ilaç salımı. |
Country Status (13)
Country | Link |
---|---|
US (1) | US9474719B2 (tr) |
EP (1) | EP2542228B1 (tr) |
JP (2) | JP2013521332A (tr) |
DK (1) | DK2542228T3 (tr) |
ES (1) | ES2660544T3 (tr) |
GB (2) | GB201003766D0 (tr) |
HU (1) | HUE037287T2 (tr) |
NO (1) | NO2542228T3 (tr) |
PL (1) | PL2542228T3 (tr) |
PT (1) | PT2542228T (tr) |
SI (1) | SI2542228T1 (tr) |
TR (1) | TR201802596T4 (tr) |
WO (1) | WO2011107749A2 (tr) |
Families Citing this family (46)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2010325960C1 (en) | 2009-12-02 | 2015-08-06 | Adamas Pharma, Llc | Amantadine compositions and methods of use |
GB201003731D0 (en) | 2010-03-05 | 2010-04-21 | Univ Strathclyde | Immediate/delayed drug delivery |
GB201003734D0 (en) | 2010-03-05 | 2010-04-21 | Univ Strathclyde | Delayed prolonged drug delivery |
US8652527B1 (en) | 2013-03-13 | 2014-02-18 | Upsher-Smith Laboratories, Inc | Extended-release topiramate capsules |
US9101545B2 (en) | 2013-03-15 | 2015-08-11 | Upsher-Smith Laboratories, Inc. | Extended-release topiramate capsules |
CN105142618A (zh) * | 2013-03-15 | 2015-12-09 | 韩国联合制药株式会社 | 提供药理及临床效应的莫沙必利每日单次施用缓释制剂 |
CN103271908B (zh) * | 2013-05-23 | 2019-02-12 | 浙江华海药业股份有限公司 | 含有替米沙坦和苯磺酸氨氯地平的口服片剂及其制备方法 |
US10154971B2 (en) | 2013-06-17 | 2018-12-18 | Adamas Pharma, Llc | Methods of administering amantadine |
WO2015023675A2 (en) | 2013-08-12 | 2015-02-19 | Pharmaceutical Manufacturing Research Services, Inc. | Extruded immediate release abuse deterrent pill |
US9492444B2 (en) | 2013-12-17 | 2016-11-15 | Pharmaceutical Manufacturing Research Services, Inc. | Extruded extended release abuse deterrent pill |
US10172797B2 (en) | 2013-12-17 | 2019-01-08 | Pharmaceutical Manufacturing Research Services, Inc. | Extruded extended release abuse deterrent pill |
CA2955229C (en) | 2014-07-17 | 2020-03-10 | Pharmaceutical Manufacturing Research Services, Inc. | Immediate release abuse deterrent liquid fill dosage form |
GB201417828D0 (en) * | 2014-10-08 | 2014-11-19 | Cereno Scient Ab | New methods and compositions |
JP2017531026A (ja) | 2014-10-20 | 2017-10-19 | ファーマシューティカル マニュファクチュアリング リサーチ サービシズ,インコーポレーテッド | 徐放性乱用抑止性液体充填剤形 |
CN105640909B (zh) | 2014-11-14 | 2019-09-20 | 正大天晴药业集团股份有限公司 | 一种含有达比加群酯的药用组合物 |
GB201420306D0 (en) * | 2014-11-14 | 2014-12-31 | Bio Images Drug Delivery Ltd | Compositions |
GB201420311D0 (en) | 2014-11-14 | 2014-12-31 | Bio Images Drug Delivery Ltd | Pharmaceutical processing |
DK3261645T3 (da) | 2015-02-27 | 2021-06-07 | Dechra Ltd | Stimulering af appetit, håndtering af vægttab og behandling af anoreksi hos hunde og katte |
AU2016225052B2 (en) | 2015-02-27 | 2021-07-08 | Cingulate Therapeutics LLC | Tripulse release stimulant formulations |
TW201717919A (zh) * | 2015-07-02 | 2017-06-01 | 國際藥品股份公司 | 雷諾多重壓縮錠劑 |
KR102203229B1 (ko) * | 2016-01-08 | 2021-01-14 | 에리슨제약(주) | 용출률이 개선된 네비보롤을 포함하는 약학적 조성물 |
CN109414423A (zh) | 2016-04-08 | 2019-03-01 | 赛伦诺科技有限公司 | 包含丙戊酸的延迟释放药物制剂和其用途 |
WO2018001582A1 (en) | 2016-06-30 | 2018-01-04 | Interquim, S.A. | Ranolazine multiple compressed tablets |
KR101841355B1 (ko) * | 2016-09-02 | 2018-03-22 | 영남대학교 산학협력단 | D-싸이클로세린의 약제학적 제형 및 이의 제조방법 |
CN106619678A (zh) * | 2016-11-17 | 2017-05-10 | 郑州郑先医药科技有限公司 | 一种治疗慢性咽炎的药物 |
WO2018145268A1 (zh) * | 2017-02-08 | 2018-08-16 | 上海市第六人民医院 | 降压药在预防和治疗骨坏死中的应用 |
CN107412180B (zh) * | 2017-06-17 | 2020-05-26 | 江西医学高等专科学校 | 一种帕利哌酮包芯片及其制备方法 |
IL272834B1 (en) | 2017-08-24 | 2024-04-01 | Adamas Pharma Llc | Compositions of amantadine, their preparation, and methods of use |
AU2018378348A1 (en) | 2017-12-05 | 2020-06-18 | Sunovion Pharmaceuticals Inc. | Crystal forms and production methods thereof |
WO2019113079A1 (en) | 2017-12-05 | 2019-06-13 | Sunovion Pharmaceuticals Inc. | Nonracemic mixtures and uses thereof |
US10799138B2 (en) | 2018-04-05 | 2020-10-13 | University Of Maryland, Baltimore | Method of administering sotalol IV/switch |
US20190381056A1 (en) | 2018-06-17 | 2019-12-19 | Axsome Therapeutics, Inc. | Compositions for delivery of reboxetine |
US10512620B1 (en) | 2018-08-14 | 2019-12-24 | AltaThera Pharmaceuticals, LLC | Method of initiating and escalating sotalol hydrochloride dosing |
US11610660B1 (en) | 2021-08-20 | 2023-03-21 | AltaThera Pharmaceuticals LLC | Antiarrhythmic drug dosing methods, medical devices, and systems |
US11696902B2 (en) | 2018-08-14 | 2023-07-11 | AltaThera Pharmaceuticals, LLC | Method of initiating and escalating sotalol hydrochloride dosing |
US11344518B2 (en) | 2018-08-14 | 2022-05-31 | AltaThera Pharmaceuticals LLC | Method of converting atrial fibrillation to normal sinus rhythm and loading oral sotalol in a shortened time frame |
US20200147093A1 (en) | 2018-10-15 | 2020-05-14 | Axsome Therapeutics, Inc. | Use of esreboxetine to treat nervous system disorders such as fibromyalgia |
US11020402B2 (en) | 2018-10-15 | 2021-06-01 | Axsome Therapeutics, Inc. | Use of reboxetine to treat narcolepsy |
WO2020212956A1 (en) * | 2019-04-18 | 2020-10-22 | Shivalik Rasayan Limited | Oral composition of otilonium bromide |
CA3142355A1 (en) | 2019-06-04 | 2020-12-10 | Sunovion Pharmaceuticals Inc. | Modified release formulations and uses thereof |
MX2019008467A (es) | 2019-07-16 | 2019-11-07 | Federico Amezcua Amezcua | Combinacion sinergica de s-ketorolaco y pregabalina en una composicion farmaceutica para el tratamiento del dolor neuropatico. |
CN110483788B (zh) * | 2019-07-19 | 2021-11-05 | 中国地质大学(武汉) | 一种MIL-53(Fe)复合材料及其制备方法和用于降解四环素的应用 |
CN110251677B (zh) * | 2019-07-29 | 2021-04-13 | 牡丹江医学院 | 用于治疗肺纤维化的药物组合物及其应用 |
CN114302712B (zh) * | 2019-09-04 | 2023-08-04 | 鲁南贝特制药有限公司 | 一种阿昔莫司多单元缓释微丸片及其制备方法 |
US11766419B2 (en) * | 2021-01-08 | 2023-09-26 | Banasthali Vidyapith | Mebeverine as soluble epoxide hydrolase inhibitor |
CN113499376A (zh) * | 2021-07-16 | 2021-10-15 | 上海交通大学医学院附属瑞金医院卢湾分院 | 治疗顽固性失眠症的联合用药物及其应用 |
Family Cites Families (37)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB8518301D0 (en) * | 1985-07-19 | 1985-08-29 | Fujisawa Pharmaceutical Co | Hydrodynamically explosive systems |
LU86099A1 (fr) | 1985-09-30 | 1987-04-02 | Pharlyse | Formes galeniques a liberation prolongee du verapamil,leur fabrication et medicaments les contenant |
US5145644A (en) | 1990-12-20 | 1992-09-08 | Allergan, Inc. | Hydrogen peroxide destroying compositions and methods of making and using same |
GB9117361D0 (en) | 1991-08-12 | 1991-09-25 | Euro Celtique Sa | Oral dosage form |
ES2106818T3 (es) | 1991-10-30 | 1997-11-16 | Glaxo Group Ltd | Composicion multicapa que contiene antagonistas de histamina o secotina. |
JPH07223970A (ja) * | 1994-02-10 | 1995-08-22 | Tanabe Seiyaku Co Ltd | 消化管内適所放出製剤 |
US5558879A (en) | 1995-04-28 | 1996-09-24 | Andrx Pharmaceuticals, Inc. | Controlled release formulation for water soluble drugs in which a passageway is formed in situ |
US5788987A (en) * | 1997-01-29 | 1998-08-04 | Poli Industria Chimica Spa | Methods for treating early morning pathologies |
US6312724B1 (en) | 1997-04-04 | 2001-11-06 | Isa Odidi | Sustained release pharmaceutical matrix tablet of pharmaceutically acceptable salts of diclofenac and process for preparation thereof |
CA2301883A1 (en) | 1997-09-11 | 1999-03-18 | Nycomed Danmark A/S | Modified release multiple-units compositions of non-steroid anti-inflammatory drug substances (nsaids) |
SE9704870D0 (sv) | 1997-12-22 | 1997-12-22 | Astra Ab | New pharmaceutical formulation I |
WO2008079102A1 (en) | 2005-05-10 | 2008-07-03 | Elan Corporation, Plc | Modified release loxoprofen compositions |
US6632451B2 (en) | 1999-06-04 | 2003-10-14 | Dexcel Pharma Technologies Ltd. | Delayed total release two pulse gastrointestinal drug delivery system |
WO2000078292A1 (fr) * | 1999-06-18 | 2000-12-28 | Takeda Chemical Industries, Ltd. | Preparations solides a desintegration rapide |
EP1064937A1 (en) * | 1999-06-28 | 2001-01-03 | Sanofi-Synthelabo | Timed dual release dosage forms comprising a short acting hypnotic or a salt thereof |
ATE376826T1 (de) | 2001-09-28 | 2007-11-15 | Mcneil Ppc Inc | Darreichungsformen zur modifizierten freisetzung |
JP2005510477A (ja) | 2001-10-08 | 2005-04-21 | サン・ファーマシューティカル・インダストリーズ・リミテッド | 抗痙攣薬の間隙をあけたドラッグデリバリーシステム |
CN1674877A (zh) * | 2002-06-07 | 2005-09-28 | 兰贝克赛实验室有限公司 | 控释的多单位药物释放系统 |
US20060177506A1 (en) | 2003-03-17 | 2006-08-10 | Shigeo Yanai | Release control compositions |
US20040241100A1 (en) * | 2003-03-17 | 2004-12-02 | Fabre Kramer Pharmaceutical, Inc. | Nasally administrable compositions of zolpidem and methods of use |
RU2391093C2 (ru) | 2003-04-24 | 2010-06-10 | Джаготек Аг | Таблетка замедленного высвобождения с заданной геометрией ядра |
JP4505859B2 (ja) * | 2003-08-08 | 2010-07-21 | 味の素株式会社 | ナテグリニド含有製剤 |
KR100782918B1 (ko) * | 2003-09-19 | 2007-12-07 | 펜웨스트 파머슈티칼즈 컴파니 | 지연 방출성 제형 |
US20050152974A1 (en) | 2003-12-31 | 2005-07-14 | Garth Boehm | Atomoxetine formulations |
US20050220877A1 (en) | 2004-03-31 | 2005-10-06 | Patel Ashish A | Bilayer tablet comprising an antihistamine and a decongestant |
GB0423964D0 (en) * | 2004-10-28 | 2004-12-01 | Jagotec Ag | Dosage form |
WO2006093353A1 (ja) | 2005-03-03 | 2006-09-08 | Takeda Pharmaceutical Company Limited | 放出制御組成物 |
US20070098788A1 (en) | 2005-10-28 | 2007-05-03 | Gore Subhash P | Non-benzodiazepine hypnotic compositions |
AR056633A1 (es) * | 2005-12-07 | 2007-10-17 | Gador Sa | Composiciones farmaceuticas de agentes hipnoticos de accion corta en forma de liberacion modificada y los procedimientos para preparar dichas formulaciones |
US9486446B2 (en) | 2006-12-28 | 2016-11-08 | Takeda Pharmaceutical Company Limited | Orally disintegrating solid preparation |
WO2008129517A2 (en) | 2007-04-23 | 2008-10-30 | Ranbaxy Laboratories Limited | A stabilized delayed release pharmaceutical composition of rabeprazole |
TW200914006A (en) * | 2007-07-12 | 2009-04-01 | Takeda Pharmaceutical | Coated preparation |
WO2009101940A1 (ja) * | 2008-02-11 | 2009-08-20 | Dainippon Sumitomo Pharma Co., Ltd. | 溶出性の改善された錠剤 |
US8240507B2 (en) | 2008-06-20 | 2012-08-14 | Graco Minnesota Inc. | Seal-retaining valve for fluid metering device |
TW201006473A (en) * | 2008-08-13 | 2010-02-16 | Orient Pharma Co Ltd | Bi-layer medicine tablet containing Zaleplon |
GB201003734D0 (en) | 2010-03-05 | 2010-04-21 | Univ Strathclyde | Delayed prolonged drug delivery |
GB201003731D0 (en) | 2010-03-05 | 2010-04-21 | Univ Strathclyde | Immediate/delayed drug delivery |
-
2010
- 2010-03-05 GB GBGB1003766.1A patent/GB201003766D0/en not_active Ceased
-
2011
- 2011-03-04 WO PCT/GB2011/000306 patent/WO2011107749A2/en active Application Filing
- 2011-03-04 NO NO11709763A patent/NO2542228T3/no unknown
- 2011-03-04 JP JP2012556575A patent/JP2013521332A/ja active Pending
- 2011-03-04 PT PT117097634T patent/PT2542228T/pt unknown
- 2011-03-04 PL PL11709763T patent/PL2542228T3/pl unknown
- 2011-03-04 DK DK11709763.4T patent/DK2542228T3/en active
- 2011-03-04 GB GB1217619.4A patent/GB2491775A/en not_active Withdrawn
- 2011-03-04 HU HUE11709763A patent/HUE037287T2/hu unknown
- 2011-03-04 EP EP11709763.4A patent/EP2542228B1/en active Active
- 2011-03-04 US US13/582,913 patent/US9474719B2/en active Active
- 2011-03-04 TR TR2018/02596T patent/TR201802596T4/tr unknown
- 2011-03-04 ES ES11709763.4T patent/ES2660544T3/es active Active
- 2011-03-04 SI SI201131426T patent/SI2542228T1/en unknown
-
2015
- 2015-11-09 JP JP2015219312A patent/JP6165824B2/ja active Active
Also Published As
Publication number | Publication date |
---|---|
PL2542228T3 (pl) | 2018-07-31 |
EP2542228A2 (en) | 2013-01-09 |
DK2542228T3 (en) | 2018-03-05 |
JP6165824B2 (ja) | 2017-07-19 |
EP2542228B1 (en) | 2017-11-29 |
GB2491775A (en) | 2012-12-12 |
JP2013521332A (ja) | 2013-06-10 |
GB201003766D0 (en) | 2010-04-21 |
GB201217619D0 (en) | 2012-11-14 |
WO2011107749A2 (en) | 2011-09-09 |
SI2542228T1 (en) | 2018-05-31 |
NO2542228T3 (tr) | 2018-04-28 |
JP2016040309A (ja) | 2016-03-24 |
PT2542228T (pt) | 2018-02-26 |
ES2660544T3 (es) | 2018-03-22 |
US9474719B2 (en) | 2016-10-25 |
HUE037287T2 (hu) | 2018-08-28 |
US20130022676A1 (en) | 2013-01-24 |
WO2011107749A3 (en) | 2012-05-03 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US11065205B2 (en) | Immediate/delayed drug delivery | |
EP2542228B1 (en) | Pulsatile drug release | |
US9283192B2 (en) | Delayed prolonged drug delivery | |
CA2467490C (en) | Pharmaceutical compositions of 5,8,14-triazatetracyclo[10.3.1.0(2,11).0(4,9)]-hexadeca-2(11)3,5,7,9-pentaene | |
Jagdale et al. | Development of press-coated, floating-pulsatile drug delivery of lisinopril | |
US20180015080A1 (en) | Compositions and methods for treatment in parkinson's disease patients | |
WO2007114376A1 (ja) | 固形医薬製剤 | |
Patil et al. | Chronomodulated press-coated pulsatile therapeutic system for aceclofenac: optimization of factors influencing drug release and lag time | |
WO2009027786A2 (en) | Matrix dosage forms of varenicline | |
MX2014010460A (es) | Formulaciones farmaceuticas que contienen flupirtina. | |
Kancharla | Formulation and Evaluation of Bi Layer Matrix Tablet of Anti Hypertensive Drug | |
Murali Krishna et al. | FORMULATION DEVELOPMENT AND EVALUATION OF TAPENTADOL HYDROCHLORIDE EXTENDED RELEASE MATRIX TABLETS | |
Jaya Prakash | Formulation Development and Evaluation of Valsartan Film Coated Tablets | |
CH | FORMULATION AND EVALUATION OF MUCOADHESIVE BUCCAL TABLETS OF CANDESARTAN | |
Raman | Development and In-Vitro Dissolution Studies of Bilayer Tablet of Metoprolol Succinate (SR) And Hydrochlorothiazide (IR). |