CN1113157A - Preparation method for medicine for treatment of rheumatoid arthritis and its powder preparation - Google Patents
Preparation method for medicine for treatment of rheumatoid arthritis and its powder preparation Download PDFInfo
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- CN1113157A CN1113157A CN 95103142 CN95103142A CN1113157A CN 1113157 A CN1113157 A CN 1113157A CN 95103142 CN95103142 CN 95103142 CN 95103142 A CN95103142 A CN 95103142A CN 1113157 A CN1113157 A CN 1113157A
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- rheumatoid arthritis
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Abstract
The invented drug for treatment of rheumatoid arthritis is a powder preparation, and its ingredients are the dried stem of Orientvine (sinomenium Acutum), dried stem and leaf of Hairy Grape, Wupifeng (a Chinese herbal medicine, used for treating rheumatic arthritis, articular swelling and pain) and sarcandra. The invented drug has the notable functions of relieving inflammation, alleviating pain and subduing swelling for curing rheumatoid arthritis, and its cure rate can be up to above 50%, and its total effective rate is 92.5%. Besides, it also has the notable curative effect for migratory arthralgia and rheumatic disease, and has no any toxic side effect, and is safe and can be taken for a long period.
Description
The present invention relates to the manufacture method of a kind of medicine and electuary thereof, particularly a kind of manufacture method for the treatment of the medicine and the electuary thereof of rheumatoid arthritis.
The medicine of treatment rheumatoid arthritis is more at present, alleviates condition of illness but effect mainly is pain relieving, just cures the symptoms, not the disease, and curative effect is all difficult to comply with one's wishes, and can not reach the effect of healing, and toxic and side effects is more obvious.
The objective of the invention is to: a kind of manufacture method that can fundamentally treat the medicine and the electuary thereof of rheumatoid arthritis disease is provided.This medicine has significant pain relieving, antiinflammatory, detumescence effect to treatment rheumatoid arthritis disease.This medicine is without any side effects, and drug safety can be taken for a long time.
Embodiment of the present invention are that drug component comprises: PAIFENGTENG, Herba Anemones vitifoliae, five wind, swollen knotweed.
The weight proportion of described component can be: PAIFENGTENG 30-50%, Herba Anemones vitifoliae 20-40%, five wind 10-20%, swollen knotweed 10-20%.
The manufacture method of the medicine instant of treatment rheumatoid arthritis disease is, PAIFENGTENG, Herba Anemones vitifoliae, five wind, the swollen knotweeds that prepare are merged decoct, medicinal liquid; In medicinal liquid, add white sugar, dextrin receipts lamb, granulate, get the electuary finished product.
In the described electuary finished product, contain white sugar 40%, contain dextrin 40-45%, containing the crude drug composition is 15-20%.Described electuary finished product dosage is: each 10～20 grams, every day 2-3 time.
Compared with the prior art, the present invention is owing to be fundamentally to treat rheumatoid arthritis disease, and drug component is reasonable, treatment rheumatoid arthritis disease there are significant pain relieving, antiinflammatory, repercussive effect, cure rate height, cure rate are more than 51%, and total effective rate is 92.5%.In addition, gout, rheumatism etc. also there is tangible curative effect.And without any side effects, drug safety can be taken for a long time.
Embodiment 1: get the PAIFENGTENG of crude drug total amount 40%, 30% Herba Anemones vitifoliae, five wind of 15%, 15% swollen knotweed merging decoction, get the decocting medicinal liquid; This decocting medicinal liquid can directly be taken; Also can in medicinal liquid, add white sugar, dextrin receipts lamb, granulate, make the electuary finished product.
In the described electuary finished product, component can be white sugar 40%, dextrin 45%, and containing the crude drug composition is 15%.Described electuary finished product dosage is: each 10 grams, every day 3 times.
Embodiment 2: get the PAIFENGTENG of crude drug total amount 50%, 25% Herba Anemones vitifoliae, five wind of 15%, 10% swollen knotweed merging decoction, get the decocting medicinal liquid; This decocting medicinal liquid can directly be taken; Also can in medicinal liquid, add white sugar, dextrin receipts lamb, granulate, make the electuary finished product.
In the described electuary finished product, component can be white sugar 40%, dextrin 40%, and containing the crude drug composition is 20%.Described electuary finished product dosage is: each 20 grams, every day 2 times.
Medicine of the present invention is made water decoction and is taken, and the potion dosage is the 15-30 gram, and medicine of the present invention in addition also can be made into other forms such as pill, capsule and takes.
Claims (5)
1, the medicine of treatment rheumatoid arthritis is characterized in that component comprises: PAIFENGTENG, Herba Anemones vitifoliae, five wind, swollen knotweed.
2, the medicine of treatment rheumatoid arthritis according to claim 1 is characterized in that, the weight proportion of described component is: PAIFENGTENG 30-50%, Herba Anemones vitifoliae 20-40%, five wind 10-20%, swollen knotweed 10-20%.
3, the medicine instant manufacture method of treatment rheumatoid arthritis is characterized in that:
A, the PAIFENGTENG with preparing, Herba Anemones vitifoliae, five wind, swollen knotweeds merge decoction, get medicinal liquid;
B, in medicinal liquid, add white sugar, dextrin and receive lamb, granulate, the electuary finished product.
4, the electuary manufacture method of the medicine of treatment rheumatoid arthritis according to claim 3 is characterized in that: in the described electuary finished product, contain white sugar 40%, contain dextrin 40-45%, containing the crude drug composition is 15-20%.
5, the medicine instant manufacture method of treatment rheumatoid arthritis according to claim 4 is characterized in that: described electuary finished product dosage is: each 10～20 grams, every day 2-3 time.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 95103142 CN1113157A (en) | 1995-03-23 | 1995-03-23 | Preparation method for medicine for treatment of rheumatoid arthritis and its powder preparation |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 95103142 CN1113157A (en) | 1995-03-23 | 1995-03-23 | Preparation method for medicine for treatment of rheumatoid arthritis and its powder preparation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN1113157A true CN1113157A (en) | 1995-12-13 |
Family
ID=5074609
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 95103142 Pending CN1113157A (en) | 1995-03-23 | 1995-03-23 | Preparation method for medicine for treatment of rheumatoid arthritis and its powder preparation |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1113157A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105770058A (en) * | 2016-04-11 | 2016-07-20 | 山东省文登整骨医院 | Traditional Chinese medicine composition for treating orthopedic diseases and preparation method and application thereof |
| CN106265851A (en) * | 2016-08-31 | 2017-01-04 | 贵州苗侗古方民族医药开发有限公司 | A kind of Seedling tea of effective reduction uric acid |
-
1995
- 1995-03-23 CN CN 95103142 patent/CN1113157A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105770058A (en) * | 2016-04-11 | 2016-07-20 | 山东省文登整骨医院 | Traditional Chinese medicine composition for treating orthopedic diseases and preparation method and application thereof |
| CN106265851A (en) * | 2016-08-31 | 2017-01-04 | 贵州苗侗古方民族医药开发有限公司 | A kind of Seedling tea of effective reduction uric acid |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C06 | Publication | ||
| PB01 | Publication | ||
| C01 | Deemed withdrawal of patent application (patent law 1993) | ||
| WD01 | Invention patent application deemed withdrawn after publication |