WO2013154202A1 - 薬品秤量装置、薬品秤量システム、薬品秤量プログラム、記録媒体 - Google Patents

薬品秤量装置、薬品秤量システム、薬品秤量プログラム、記録媒体 Download PDF

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Publication number
WO2013154202A1
WO2013154202A1 PCT/JP2013/061184 JP2013061184W WO2013154202A1 WO 2013154202 A1 WO2013154202 A1 WO 2013154202A1 JP 2013061184 W JP2013061184 W JP 2013061184W WO 2013154202 A1 WO2013154202 A1 WO 2013154202A1
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WIPO (PCT)
Prior art keywords
medicine
prescription
information
drug
weighing
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PCT/JP2013/061184
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English (en)
French (fr)
Japanese (ja)
Inventor
湯山　裕之
田中　徹
学司 後藤
Original Assignee
株式会社湯山製作所
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=49327756&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO2013154202(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by 株式会社湯山製作所 filed Critical 株式会社湯山製作所
Priority to JP2014510222A priority Critical patent/JP6529259B2/ja
Priority to KR1020147031574A priority patent/KR102048262B1/ko
Publication of WO2013154202A1 publication Critical patent/WO2013154202A1/ja

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    • G—PHYSICS
    • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H20/00—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance
    • G16H20/10—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J3/00—Devices or methods specially adapted for bringing pharmaceutical products into particular physical or administering forms
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65B—MACHINES, APPARATUS OR DEVICES FOR, OR METHODS OF, PACKAGING ARTICLES OR MATERIALS; UNPACKING
    • B65B1/00—Packaging fluent solid material, e.g. powders, granular or loose fibrous material, loose masses of small articles, in individual containers or receptacles, e.g. bags, sacks, boxes, cartons, cans, or jars
    • B65B1/30—Devices or methods for controlling or determining the quantity or quality or the material fed or filled
    • G—PHYSICS
    • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H20/00—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance
    • G16H20/10—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients
    • G16H20/13—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered from dispensers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J2200/00—General characteristics or adaptations
    • A61J2200/30—Compliance analysis for taking medication
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J2205/00—General identification or selection means
    • A61J2205/10—Bar codes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J2205/00—General identification or selection means
    • A61J2205/60—General identification or selection means using magnetic or electronic identifications, e.g. chips, RFID, electronic tags

Definitions

  • the present invention relates to a drug weighing device used for weighing drugs according to a prescription and its peripheral technology.
  • pharmacists weigh each drug using an electronic balance while referring to a prescription. Specifically, the pharmacist refers to the prescription, confirms the necessary medicine, and takes out the medicine container containing the medicine from the medicine shelf or the like. Then, the pharmacist weighs the medicine stored in the medicine container with an electronic balance according to the prescription amount recorded in the prescription.
  • Patent Document 1 discloses a chemical weighing apparatus having an electronic balance function and a chemical audit function.
  • this medicine weighing device not only the medicine is weighed, but also an audit of whether or not the weighing value of the medicine is a normal dose (a proper amount to be taken once a day or once) set in advance for each medicine. Is possible.
  • the medicine weighing device when used alone without cooperation with a host system such as a dispensing support system used in a hospital or a dispensing pharmacy, prescription data can be acquired from the host system. Can not. In this case, the medicine weighing device can only record the history of who weighed which medicine and how many grams, and compares the medicine name recorded in the medicine container with the medicine name recorded in the prescription. (So-called audit work) was not possible. Therefore, when weighing the drug with the drug weighing device, the drug name recorded in the prescription and the drug name recorded in the drug container are checked only by the visual inspection of the pharmacist. Concerned.
  • An object of the present invention is to provide a drug weighing device that can support accurate drug weighing according to a prescription.
  • the drug weighing device includes weighing means, prescription information reading means, stored medicine information reading means, and control means.
  • the weighing means weighs the drug.
  • the prescription information reading unit reads prescription information including prescription drug identification information for identifying one or a plurality of prescription drugs recorded in the prescription from the prescription.
  • the stored medicine information reading means reads stored medicine information including stored medicine identification information for identifying the stored medicine recorded in the medicine container from the medicine container.
  • the control means selects the prescription drug as a weighing target, A weighing screen for weighing the prescription drug is displayed on the display means.
  • the chemical weighing system includes a plurality of charging units into which chemicals are charged, a chemical packaging device having a packaging unit for packaging the chemicals charged into each of the charging units, and the chemical weighing device.
  • the medicine packaging apparatus includes an information reading unit that reads information from the recording medium, and a loading destination display unit that selects and displays one of the loading units based on the weighed drug information read by the information reading unit. .
  • the medicine weighing program is a program for causing a computer to execute a prescription information reading process, a stored medicine information reading process, and a control process.
  • the prescription information reading step reads prescription information including prescription drug identification information for identifying one or a plurality of prescription drugs recorded in the prescription from the prescription.
  • stored medicine information reading step stored medicine information including stored medicine identification information for identifying the stored medicine recorded in the medicine container is read from the medicine container.
  • the control step corresponds to any one of the prescription drugs indicated by the prescription drug identification information read by the prescription information reading step, the stored medicine indicated by the stored medicine identification information read by the stored medicine information reading step.
  • the prescription drug is selected as a weighing target, and a weighing screen for the prescription drug as a weighing target is displayed on the display means.
  • the recording medium according to the present invention is a computer-readable recording medium in which the medicine weighing program is recorded.
  • FIG. 1 is a block diagram showing a schematic configuration of a chemical weighing system according to an embodiment of the present invention.
  • FIG. 2 is a schematic diagram showing a schematic configuration of a drug weighing device of the drug weighing system according to the embodiment of the present invention.
  • FIG. 3 is a principal block diagram showing an example of the data structure of the generic drug master.
  • FIG. 4 is a schematic diagram showing a schematic configuration of a medicine packaging device of the medicine weighing system according to the embodiment of the present invention.
  • FIG. 5 is a flowchart showing an example of a procedure of a drug weighing process executed by the drug weighing apparatus.
  • FIG. 6 is a diagram showing an example of a prescription screen displayed in the medicine weighing process.
  • FIG. 1 is a block diagram showing a schematic configuration of a chemical weighing system according to an embodiment of the present invention.
  • FIG. 2 is a schematic diagram showing a schematic configuration of a drug weighing device of the drug weighing system according to the embodiment of the present invention.
  • FIG. 7 is a diagram showing an example of a weighing screen displayed in the chemical weighing process.
  • FIG. 8 is a diagram showing an example of a progress screen displayed in the chemical weighing process.
  • FIG. 9 is a diagram illustrating an example of a warning screen, a confirmation screen, and a warning screen displayed in the chemical weighing process.
  • FIG. 10 is a diagram showing an example of the registration screen for the generic drug master.
  • FIG. 11 is a flowchart showing an example of the procedure of the medicine packaging process executed by the medicine packaging apparatus.
  • FIG. 12 is a flowchart showing another example of the procedure of the medicine packaging process executed by the medicine packaging apparatus.
  • FIG. 13 is a flowchart showing another example of the procedure of the medicine packaging process executed by the medicine packaging apparatus.
  • FIG. 11 is a flowchart showing an example of the procedure of the medicine packaging process executed by the medicine packaging apparatus.
  • FIG. 14 is a flowchart showing another example of the procedure of the medicine packaging process executed by the medicine packaging apparatus.
  • FIG. 15 is a diagram for explaining the prescription batch reading mode.
  • FIG. 16 is a diagram showing another example of a weighing screen displayed in the chemical weighing process executed by the book item weighing apparatus.
  • FIG. 17 is a block diagram showing another example of the chemical weighing system.
  • FIG. 18 is a flowchart for explaining an example of the procedure of prescription input processing executed by the book item weighing apparatus.
  • FIG. 19 is a conceptual diagram for explaining the execution result of the recipe dividing process executed by the book weighing apparatus.
  • FIG. 20 is a conceptual diagram for explaining the execution result of the recipe collecting process executed by the book item weighing apparatus.
  • FIG. 21 is a diagram showing an example of a system interlocking selection screen displayed on the book item weighing apparatus.
  • FIG. 22 is a flowchart for explaining an example of the procedure of the display control process executed by the book item weighing apparatus.
  • FIG. 23 is a diagram showing an example of a prescription screen displayed on the book item weighing apparatus.
  • FIG. 24 is a diagram showing an example of a prescription screen displayed on the book item weighing apparatus.
  • FIG. 25 is a diagram showing an example of a prescription list screen displayed on the book item weighing apparatus.
  • FIG. 26 is a diagram showing an example of a prescription list screen displayed on the book item weighing apparatus.
  • FIG. 27 is a diagram showing an example of a prescription drug information screen displayed on the book item weighing apparatus.
  • FIG. 28 is a diagram showing an example of a recipe list screen displayed on the book item weighing apparatus.
  • FIG. 29 is a diagram showing an example of a recipe list screen displayed on the book item weighing apparatus.
  • FIG. 30 is a diagram showing an example of a prescription drug information screen displayed on the book item weighing apparatus.
  • FIG. 31 is a diagram showing an example of a patient ID input screen displayed on the book weighing device.
  • FIG. 32 is a flowchart for explaining another example of the generic drug use process executed by the book item weighing apparatus.
  • FIG. 33 is a diagram showing an example of a prescription screen displayed on the book item weighing apparatus.
  • FIG. 34 is a flowchart for explaining an example of the procedure of the prescription drug changing process executed by the book item weighing apparatus.
  • FIG. 35 is a diagram showing an example of a prescription screen displayed on the book item weighing apparatus.
  • FIG. 36 is a diagram showing an example of a medicine list screen displayed on the book item weighing apparatus.
  • FIG. 37 is a flowchart for explaining an example of the procedure of the registration process for generic drugs executed by the book weighing device.
  • FIG. 38 is a diagram showing an example of a maintenance screen displayed on the book item weighing apparatus.
  • FIG. 39 is a flowchart for explaining an example of the procedure of the starting process executed in the book item weighing apparatus.
  • FIG. 40 is a diagram showing an example of a machine selection screen displayed on the book weighing device.
  • FIG. 41 is a diagram showing an example of a packaging input screen displayed on the medicine packaging apparatus.
  • FIG. 42 is a diagram showing an example of a packaging input screen displayed on the medicine packaging apparatus.
  • FIG. 43 is a diagram showing an example of a print image of drug information printed by the medicine packaging apparatus.
  • FIG. 44 is a diagram showing an example of a print image of drug information printed by the medicine packaging apparatus.
  • a drug weighing system 1 includes a drug weighing device 10 for weighing drugs and a drug packaging device 20 for packaging drugs.
  • a user such as a doctor or a pharmacist places a medicine on a medicine sheet 30 (an example of a medicine placement member) and measures the medicine with the medicine weighing device 10. Thereafter, the user moves the medicine sheet 30 on which the weighed medicine is placed to the medicine packaging apparatus 20 and puts the medicine into the medicine packaging apparatus 20. Thereby, the medicine is packaged separately by the medicine packaging apparatus 20 one by one.
  • medicine packaging apparatus 20 may have each function of the said chemical
  • medicine packaging apparatus 20 corresponds to the chemical
  • what is necessary is just to employ
  • the chemical weighing apparatus 10 includes a control unit 11, a balance unit 12, a touch panel 13, an RFID reader / writer 14, a data storage unit 15, a USB port 16, a barcode reader 17, a printer 18, and the like.
  • the control unit 11, the balance unit 12, and the touch panel 13 are integrally provided in the apparatus main body of the chemical weighing apparatus 10.
  • the drug weighing device 10 can be used for weighing drugs in various dosage forms such as powders, liquids, tablets, and heat agents (packed with a predetermined amount of powder or tablets).
  • the control unit 11 is a computer that includes a CPU, a ROM, a RAM (such as an EEPROM), and the like, and controls the drug weighing device 10 in an integrated manner.
  • the CPU is a processor that executes various arithmetic processes according to various programs.
  • the ROM is a non-volatile memory in which programs such as BIOS executed by the CPU are stored in advance.
  • the RAM is a volatile memory or a non-volatile memory used for development of various programs by the CPU and temporary storage of data in various arithmetic processes.
  • the balance unit 12 is an example of a weighing means for weighing a chemical placed on a stainless steel balance table 19.
  • the balance unit 12 is a balance unit that is also used in a well-known electronic balance including a balance circuit, a force coil, a current / voltage conversion circuit, an A / D conversion circuit, and the like.
  • the weight of the medicine weighed by the balance unit 12 is input to the control unit 11 as digital data.
  • a windshield cover (not shown) for preventing the powder on the balance table 19 from being scattered by the wind can be attached to and detached from the chemical weighing device 10.
  • the medicine sheet 30 is provided with an RFID tag 31 as a recording medium on which various types of information are read and written.
  • the RFID tag 31 is provided at a position where the RFID reader / writer 14 can read and write data when the medicine sheet 30 is placed on the balance table 19.
  • the said balance unit 12 makes the value which deducted the weight of the said medicine sheet
  • the touch panel 13 detects an operation of a display unit such as a liquid crystal panel or an organic EL panel that displays various screens and various information according to a control instruction from the control unit 11, and an operation key displayed on the display unit. And a detection unit for inputting a detection signal to the control unit 11. That is, the touch panel 13 also serves as a display unit and an input unit in the chemical weighing device 10. Specifically, the control unit 11 causes the touch panel 13 to display a weighing value weighed by the balance unit 12 (see FIG. 7).
  • a display unit such as a liquid crystal panel or an organic EL panel that displays various screens and various information according to a control instruction from the control unit 11, and an operation key displayed on the display unit.
  • the control unit 11 causes the touch panel 13 to display a weighing value weighed by the balance unit 12 (see FIG. 7).
  • the RFID reader / writer 14 records information on an RFID tag or an RFID label using a radio communication technology of RFID (Radio Frequency Identification), or reads information from the RFID tag or the RFID label.
  • the RFID reader / writer 14 is provided adjacent to the balance table 19, and reads and writes information from and to the RFID tag 31 when the medicine sheet 30 is placed on the balance table 19. Used.
  • the RFID reader / writer 14 may be incorporated in the chemical weighing device 10.
  • FIG. 2 shows an example in which the RFID reader / writer 14 is arranged on the left side of the balance table 19, but it may be arranged behind the balance table 19.
  • the RFID reader / writer 14 is provided in the lower layer of the balance table 19, and the RFID tag 31 is attached to the medicine sheet 30.
  • a configuration provided on the bottom surface of the can also be considered. Thereby, when the medicine sheet 30 is placed on the balance table 19, the RFID reader / writer 14 can read / write information from / to the RFID tag 31 regardless of the orientation of the medicine sheet 30.
  • the data storage unit 15 stores various data such as a control program such as a drug weighing program executed by the control unit 11, a drug master (corresponding to drug information), a generic drug master (corresponding to generic drug information), and the like. It is a USB memory and can be attached to and detached from the chemical weighing device 10. Specifically, the data storage unit 15 is attached to and detached from the attachment part of the USB port 16 exposed by removing an attachment / detachment cover (not shown) provided on the back surface of the drug weighing device 10. Here, the detachable cover (not shown) can be opened and closed without disassembling the control unit 11, the balance unit 12, the touch panel 13 and the like of the chemical weighing device 10.
  • the data storage unit 15 can be attached to and detached from the chemical weighing device 10 without any problem in the measurement method. Therefore, various data such as the drug weighing program, the drug master, and the generic drug master can be easily updated by appropriately replacing the data storage unit 15.
  • the data storage unit 15 is not limited to a USB memory, and may be a recording medium such as another flash memory, a memory card, or a disk.
  • the data storage unit 15 in which the medicine weighing program is recorded corresponds to the recording medium according to the present invention.
  • the chemical weighing program is software that causes a computer such as the control unit 11 to execute each processing step of a chemical weighing process (see FIG. 5) described later.
  • the medicine weighing program runs on an OS such as an Android (registered trademark) installed in the control unit 11.
  • the medicine weighing program includes an audit of whether or not the weighing value of the medicine is within a range of a normal dose (appropriate amount to be taken once a day or once) set for each medicine by the control unit 11.
  • An audit program is also included. Therefore, the drug weighing device 10 can perform both drug weighing and normal dose auditing alone without using another information processing device such as a computer.
  • the said control part 11 when performing the audit process which concerns here corresponds to an auditing means.
  • the drug master includes drug code, drug name, JAN code (or RSS), drug bottle code, classification (drug form: powder, tablet, liquid medicine, topical medicine, etc.), specific gravity, drug type (ordinary drug, poison, Narcotics, powerful drugs, antipsychotics, therapeutic drugs, etc.), formulation changes, excipients, precautions, normal dose (corresponding to appropriate amount information), and information on prohibition of simultaneous use.
  • the data storage unit 15 is an example of a medicine information storage unit.
  • the JAN code is information corresponding to a stored medicine name (an example of stored medicine identification information) recorded in a medicine bottle (an example of a medicine container) supplied from a pharmaceutical manufacturer.
  • the JAN code is recorded (described) by a bar code.
  • the medicine bottle code is information corresponding to the name of the medicine stored in the medicine bottle when the medicine in the medicine box supplied from the pharmaceutical manufacturer is subdivided into medicine bottles (an example of a medicine container).
  • the medicine bottle code is recorded by a bar code.
  • the control unit 11 can obtain the names of stored medicines corresponding to the barcodes by referring to the pharmaceutical master.
  • the drug name (prescription drug name, stored drug name, original drug name, as information for identifying the drug (prescription drug identification information, contained drug identification information, original drug identification information, generic drug identification information),
  • the case of using the generic drug name) will be described as an example, but the present invention is not limited thereto, and a drug code or the like may be used.
  • the control unit 11 and the control unit 21 which will be described later compare drug types, the drug name is compared, the drug code is compared, the drug name indicated by the drug code is specified, and the drug name It is conceivable to adopt various methods such as comparing the chemical codes, specifying the chemical codes indicated by the chemical names and comparing the chemical codes, or combining any of these in combination.
  • the regular dose is an appropriate amount to be taken in one day or once, which is predetermined for each medicine.
  • the simultaneous dosing prohibition information is information relating to a medicine that is predetermined for each medicine and that is prohibited from being taken at the same time.
  • the normal dose and the simultaneous dosing prohibition information are used in an audit process executed by the control unit 11 according to the audit program. Specifically, the control unit 11 stores in the data storage unit 15 an audit as to whether or not the weighing value weighed by the balance unit 12 is within the range of an appropriate amount preset for each medicine. Based on the usual dose. Further, the control unit 11 performs an audit on the data storage unit 15 to check whether or not a plurality of medicines included in prescription information read by a bar code reader 17 described later is prohibited from being taken at the same time. This is performed based on the stored simultaneous prohibition information.
  • the control unit 11 When the weighing value is outside the range of the normal dose, or when there is a medicine that is prohibited in advance from taking the medicine recorded in the prescription, the control unit 11 It is conceivable to display a warning on the touch panel 13 or the like. The control unit 11 displays the warning with characters, images, sounds, or light. Thereby, prescription of a medicine exceeding the normal dose or prescription of a plurality of medicines causing a change in composition or side effects when taken at the same time can be prevented at the medicine weighing stage in the medicine weighing device 10. it can.
  • the generic drug master includes the generic drug name, drug name, JAN code (or RSS), drug bottle code, classification (dosage form: powder, tablet, liquid medicine, topical drug, etc.), specific gravity, drug type (ordinary) Drugs, poisons, narcotics, powerful drugs, antipsychotics, therapeutic drugs, etc.), formulation changes, excipients, precautions, normal dose (corresponding to appropriate amount information), information on prohibition of simultaneous use, etc. are stored. Even when the generic drug is weighed in the drug weighing device 10, the control process by the control unit 11 based on the normal dose or the simultaneous dosing prohibition information is performed in the same manner as described above.
  • a correspondence relationship between a plurality of generic drug names (an example of generic drug identification information) and a plurality of generic drug names (an example of generic drug identification information) is defined.
  • the name of the generic drug and the generic drug name having the same medicinal effect are stored in association with each other.
  • the generic drug master stores the generic drug name and the generic drug name in association with the generic name of the drug.
  • the data storage unit 15 is an example of generic drug information storage means.
  • the control unit 11 can obtain the name of the generic drug corresponding to each barcode by referring to the generic drug master.
  • the drug master and the generic drug master are read by the control unit 11 or edited by the control unit 11.
  • FIG. 3 is a principal block diagram schematically showing a part of the data structure of the drug master and the generic drug master.
  • medicine codes A, B, and C and medicine names AA, BB, and CC are stored in association with each other in the medicine master.
  • the generic drug master includes generic drug codes A ′, A ′′, generic drug codes B ′, B ′′, generic drug names AA ′, AA ′′, generic drug names B ′, BB ′′. They are stored in association with each other.
  • the generic drug codes A ′ and A ′′ are associated with the drug code A which is a generic drug corresponding to the generic drug codes A ′ and A ′′.
  • the generic drug codes B ′ and B ′′ are associated with the drug code B, which is a generic drug corresponding to the generic drug codes B ′ and B ′′. Accordingly, the control unit 11 determines the correspondence between the medicine code A and the generic drug codes A ′ and AA ′′, and the correspondence between the medicine code B and the generic drug codes B ′ and BB ′′. Each can be known.
  • FIG. 3 shows a state in which no generic drug is registered for the drug code C.
  • the USB port 16 is a communication interface that communicates with a USB device according to the USB (Universal Serial Bus) communication standard.
  • the USB port 16 has at least three connection portions to which the data storage unit 15, the barcode reader 17 and the printer 18 are attached and detached.
  • the drive power for the barcode reader 17 and the printer 18 is supplied from the USB port 16.
  • the chemical weighing device 10, the barcode reader 17, and the printer 18 may be individually connected to a commercial AC power source.
  • connection method between the barcode reader 17 and the printer 18 and the chemical weighing device 10 is not limited to USB, and may be, for example, LAN or IEEE. Further, the barcode reader 17 and the printer 18 may be connected so as to be communicable with the medicine weighing device 10 by wireless USB, wireless LAN, or the like. Further, the bar code reader 17 may be provided integrally with the drug weighing device 10.
  • the bar code reader 17 reads information from a one-dimensional bar code such as a JAN code or RSS and a two-dimensional code such as a QR code (registered trademark).
  • a one-dimensional bar code such as a JAN code or RSS
  • a two-dimensional code such as a QR code (registered trademark).
  • the control unit 11 uses the barcode reader 17 to store prescription information including one or more prescription drug names (an example of prescription drug identification information) recorded (described) in a prescription.
  • prescription information including one or more prescription drug names (an example of prescription drug identification information) recorded (described) in a prescription.
  • a two-dimensional code such as a QR code (registered trademark) recorded (described) in the prescription.
  • the two-dimensional code is a display-type code having information in the horizontal direction and the vertical direction, and can encode more information than a bar code having information only in the horizontal direction, thereby reducing the printing area. It can also be made smaller.
  • the said control part 11 when performing the reading process which concerns here corresponds to a prescription information reading means.
  • the prescription information includes prescription delivery date, patient ID, patient name, patient birth date, dosage form information (internal use, topical use, etc.), drug information (drug code, drug name, dose), usage information ( Etc.) after 3 meals a day).
  • the control unit 11 uses the barcode reader 17 to record the stored medicine information including the stored medicine name recorded (described) in the medicine bottle with the barcode. Read from the (description) JAN code or vial code.
  • the said control part 11 when performing the reading process which concerns here corresponds to an accommodation chemical
  • the method of reading the prescription information and the contained medicine information from the prescription or the medicine bottle is not limited to using a barcode, and may use a character recognition technique or an image recognition technique.
  • an information recording medium such as an RFID tag or an RFID label is provided in the medicine bottle, and stored medicine information including the name of the medicine stored in the medicine bottle is recorded on the information recording medium. It is done.
  • the medicine weighing device 10 includes wireless reading means such as an RFID reader for reading information from the information recording medium by wireless communication, and the control unit 11 is the information recording medium provided in the medicine bottle. It is conceivable that the stored medicine information is read by the wireless reading means.
  • the medicine weighing device 10 includes wireless reading means such as an RFID reader that reads information from the information recording medium by wireless communication, and the control unit 11 uses the information recording medium provided in the prescription. It can be considered that the prescription information is read by the wireless reading means.
  • the control unit 11 reads one of the stored medicine information and the prescription information with the barcode reader 17 (code reading unit) and the other with the wireless reading unit is also conceivable.
  • the medicine weighing apparatus 10 includes the wireless reading unit instead of the barcode reader 17 (code reading unit), and the control unit 11 transmits both the stored medicine information and the prescription information to the wireless unit.
  • a configuration in which reading is performed by a reading unit is also conceivable.
  • the control unit 11 selectively selects the barcode reader 17 or the wireless reading unit. It is possible to read the stored medicine information and the prescription information.
  • the printer 18 prints out print data input from the control unit 11 via the USB port 16. Specifically, the printer 18 is used for printing a weighing result or the like by the chemical weighing device 10. A printing layout of the weighing result is set in advance, or can be arbitrarily set in the initial setting of the chemical weighing device 10. Further, in the medicine weighing apparatus 10, the control unit 11 can input the prescription information to the printer 18 to print a barcode or a two-dimensional code indicating the prescription information together with the weighing result. Thereby, the medicine packaging apparatus 20 can execute a packaging operation according to the prescription information printed by the printer 18.
  • the medicine packaging apparatus 20 includes a control unit 21, a packaging unit 22, a touch panel 23, an RFID reader / writer 24, a supply hopper 25, and the like.
  • the medicine packaging device 20 wraps the powdered medicine one by one and is also called a powder medicine packaging machine.
  • the control unit 21 is a computer that includes a CPU, a ROM, a RAM (such as an EEPROM), and the like, and controls the medicine packaging device 20 in an integrated manner.
  • the CPU is a processor that executes various arithmetic processes according to various programs.
  • the ROM is a non-volatile memory in which programs such as BIOS executed by the CPU are stored in advance. For example, a medicine packaging program for causing the control unit 21 to execute a medicine packaging process described later is stored in the ROM.
  • the RAM is a volatile memory or a non-volatile memory used for development of various programs by the CPU and temporary storage of data in various arithmetic processes.
  • the supply hopper 25 includes two hoppers 25A and 25B (corresponding to the charging section) for charging powder.
  • the packaging unit 22 is divided by the dividing unit 221 (an example of a dividing unit) that divides the powdered medicine into each of the hoppers 25A and 25B into one dose unit according to the prescription information and the dividing unit 221.
  • a packaging unit 222 (which is an example of packaging means) for packaging the powder, and performing a packaging operation for packaging the powder in single dose units.
  • the dividing unit 221 distributes the powder charged in each of the hoppers 25A and 25B evenly to an annular distribution tray rotated by a vibration feeder, and then scrapes the annular distribution tray while rotating the annular distribution tray by a predetermined angle.
  • the packaging unit 22 The operation of quantitatively discharging to the packaging unit 22 is performed. Therefore, in the packaging unit 22, one type of powdered medicine put into either the hopper 25A or 25B is packaged into a wrapping paper (medicine package) in a single dose unit, or put into the hoppers 25A and 25B. Two types of powdered powders can be packaged in the same wrapping paper in one dose unit.
  • the medicine packaging apparatus 20 configured in this way is also disclosed in Japanese Patent No. 462433.
  • the number of hoppers provided in the supply hopper 25 may be three or more.
  • a plurality of powders are packaged into wrapping paper in a single dose unit by charging powder into the hopper 25A or the hopper 25B a plurality of times and repeating equal distribution to the annular distribution tray. It is also possible to do.
  • the touch panel 23 detects operations of a display unit such as a liquid crystal panel or an organic EL panel that displays various screens and various information according to a control instruction from the control unit 21, and an operation key displayed on the display unit. And a detection unit for inputting a detection signal to the control unit 21. That is, the touch panel 23 also serves as a display unit and an input unit in the medicine packaging device 20.
  • a display unit such as a liquid crystal panel or an organic EL panel that displays various screens and various information according to a control instruction from the control unit 21, and an operation key displayed on the display unit.
  • a detection unit for inputting a detection signal to the control unit 21. That is, the touch panel 23 also serves as a display unit and an input unit in the medicine packaging device 20.
  • the RFID reader / writer 24 records information on an RFID tag or an RFID label using an RFID wireless communication technology, or reads information from the RFID tag or RFID label.
  • the RFID reader / writer 24 is built in a predetermined position of the medicine packaging device 20, and is used to read / write information from / to the RFID tag 31 when the medicine sheet 30 is placed at the predetermined position. It is done.
  • the chemical weighing process is a process executed by the control unit 11 when the chemical weighing apparatus 10 is turned on.
  • prescription, prescription delivery date, patient ID, patient name, patient birth date, dosage form information (internal use, external use, etc.), drug information (drug code, drug name, dose), usage information (1 day A case where 3 times after each meal is recorded with a two-dimensional code indicating such information will be described as an example.
  • the prescription drug names include three types of drugs, drug A, drug B, and drug C.
  • step S1 the control unit 11 waits for reading of prescription information (No side of S1). Specifically, the control unit 11 determines that the prescription information has been read when the barcode reader 17 reads a two-dimensional code recorded in the prescription. Then, when the user holds the two-dimensional code of the prescription over the barcode reader 17 and the barcode reader 17 reads the two-dimensional code (Yes side of S1), the control unit 11 performs the process in step S2. To migrate.
  • the prescription information read from the two-dimensional code includes prescription delivery date, patient ID, patient name, patient date of birth, dosage form information (internal use, external use, etc.), drug information (drug code, drug) Information recorded in the prescription, such as name, dose), usage information (such as after 3 meals per day).
  • the bar code reader 17 is always readable when, for example, the drug weighing device 10 is powered on. It is also conceivable that the control unit 11 shifts the barcode reader 17 to a readable state for a certain period in response to an operation input for starting weighing on the touch panel 13.
  • Step S2> the control unit 11 displays the prescription screen 40 on the touch panel 13 based on the prescription information read in step S1.
  • FIG. 6 (A) and FIG. 6 (B) show an example of the prescription screen 40, respectively.
  • the dispenser name, patient name, age, weight, prescription days, fractions, drug name, dosage form (spread / tablet), prescription amount, etc. are displayed.
  • the medicine A, the medicine B, and the medicine C are displayed as prescription medicine names on the medicine display unit 401.
  • the medicine A has a powder form of “powder” and a prescription amount of “0.9 g”
  • the medicine B has a dosage form of “powder” and a prescription amount of “1.2 g”.
  • the medicine C has a dosage form of “powder” and a prescription amount of “0.6 g”.
  • the display mode for displaying the medicine name and the like in this way is referred to as a medicine name display mode.
  • the name of the dispenser On the other hand, on the prescription screen 40 shown in FIG. 6B, the name of the dispenser, patient name, age, weight, number of days for prescription, number of minutes, etc. are displayed. Is not displayed.
  • the display mode in which the medicine name or the like is not displayed is referred to as a medicine name non-display mode.
  • the medicine name non-display mode is a display mode for causing the dispenser to perform the dispensing operation while viewing the paper prescription by not displaying the medicine name or the like on the prescription screen 40.
  • the medicine name non-display mode when the prescription information read from the two-dimensional code is different from the prescription recording content for some reason, the pharmacist can recognize the malfunction. .
  • comments such as caution information arbitrarily recorded in the prescription may not be included in the two-dimensional code, and in such operations where information not included in the two-dimensional code is recorded in the prescription,
  • the medicine name non-display mode in which a person needs to surely see the prescription is preferable.
  • the control unit 11 displays an initial setting screen related to the drug weighing program according to the operation of the touch panel 13, and the drug name display mode or the mode according to the operation according to the initial setting screen.
  • the medicine name non-display mode is switched.
  • step S3 the control unit 11 waits for reading of the stored medicine name (No side of S3). Specifically, when the stored medicine information indicated by the JAN code or the medicine bottle code recorded in the medicine bottle is read by the bar code reader 17, the control unit 11 reads the medicine name contained in the medicine. to decide. When the user holds the JAN code or medicine bottle code of the medicine bottle over the barcode reader 17 and the barcode reader 17 reads the JAN code or medicine bottle code (Yes side of S3), the control The unit 11 shifts the process to step S4.
  • the control unit 11 stores the weighing result when the stored medicine name is first read and weighed, and when the prescription information is read after that, the prescription information and the weighing are stored. Matching the results is also conceivable as another embodiment.
  • step S4 the control unit 11 branches the process according to the collation result between the stored medicine name in the stored medicine information read in step S3 and the stored medicine name in the prescription information read in step S1. To do. Specifically, in step S4, the control unit 11 determines whether the stored medicine name corresponds to one of the prescription medicine names.
  • step S5 the contained medicine name must correspond to any of the prescription medicine names. If (No in S4), the process proceeds to step S13.
  • step S ⁇ b> 5 the control unit 11 selects a prescription drug name that matches the stored medicine name among prescription drug names included in the prescription information as a weighing target. That is, when the contained medicine name corresponds to any of the prescription medicine names, the prescription medicine name to be weighed is automatically selected from the prescription medicine names included in the prescription information.
  • the user can check the stored medicine name and the prescription medicine name in the medicine weighing device 10 only by the operation of causing the barcode reader 17 to read the JAN code or medicine bottle code recorded in the medicine bottle. Selection of the drug to be weighed can be realized. Accordingly, when a plurality of prescription drug names are included in the prescription information, an operation for selecting a prescription drug name to be weighed can be omitted, and the dispensing efficiency by a user such as a doctor or a pharmacist is improved. be able to.
  • step S ⁇ b> 6 the control unit 11 causes the touch panel 13 to display a weighing screen 41 for weighing a drug having a prescription drug name corresponding to the stored drug name from the prescription information. At this time, the control unit 11 displays on the weighing screen 41 the measurement value of the drug by the balance unit 12 and the target value of the measurement of the drug with the prescription drug name.
  • FIG. 7 shows an example of the weighing screen 41.
  • the weighing screen 41 shown in FIG. 7 is displayed when the medicine A is read in the step S3.
  • the medicine name is “medicine A” and the target value “0.9 g” is the prescription amount. ”And the actual weighing value“ 0.0 g ”by the balance unit 12 are displayed.
  • the weighing screen 41 shown in FIG. 7 displays a determination key 411 operated to complete weighing relating to the prescription drug name.
  • the determination key 411 embodied on the touch panel 13 is an operation unit for inputting completion of weighing for each prescription drug name, and is an example of a first input unit according to the present invention.
  • FIG. 16 is a view showing a weighing screen P16 which is another example of the weighing screen 41.
  • the control unit 11 displays an image or text.
  • the detection display part P161 indicated by the above is displayed. Thereby, the user can easily confirm by the display on the detection display unit P161 that information can be written in the RFID tag 31 by the RFID reader / writer 14.
  • the control unit 11 hides the detection display unit P161 when the RFID tag 31 is not detected by the RFID reader / writer 14.
  • the control unit 11 displays on the touch panel 13 that writing to the RFID tag 31 cannot be performed at a timing when information writing to the RFID tag 31 is originally executed.
  • the weighing screen P16 displays information such as the name of the drug to be weighed, the normal dose, the target amount, and the current weighing value as the weighing state in the drug weighing device 10, and the current amount relative to the target amount.
  • the barometer display part P162 which shows the weighed value in the image is displayed.
  • step S7 the said control part 11 waits for completion of the weighing of the said prescription drug name (No side of S7). Specifically, the control unit 11 determines that the weighing of the prescription drug name is completed by operating the determination key 411 displayed on the weighing screen 41 as shown in FIG. And if the said control part 11 judges that the measurement of the said prescription medicine name is completion (Yes side of S7), it will transfer a process to step S8. In addition, the said control part 11 memorize
  • the said prescription medicine name It is also conceivable to determine that the weighing is completed.
  • “ ⁇ ” is displayed on the weighing screen shown in FIG.
  • the control unit 11 can determine that the drug sheet 30 has been lifted on the condition that the weighing value by the balance unit 12 instantaneously becomes zero.
  • the medicine sheet 30 is lifted, information cannot be recorded on the RFID tag 31 in step S9 described later.
  • the control unit 11 records information (S9) on the RFID tag 31 whenever necessary when the weighing value obtained by the balance unit 12 is continuously stabilized for the predetermined time.
  • the final weighing value is recorded in the RFID tag 31.
  • information excluding the weighing value by the weighing unit 12 is written when the medicine sheet 30 is placed on the medicine weighing device 10, and thereafter, the weighing value It is possible to update only at any time. Thereby, even if the time from when the weighing value is stabilized for a predetermined time to when the drug sheet 30 is lifted is a short time, the weighing value can be updated to the latest information within the short time. .
  • step S ⁇ b> 8 the control unit 11 causes the touch panel 13 to display a progress screen 42 indicating the progress of weighing the prescription drug name in the prescription information.
  • 8A and 8B show examples of the progress screen 42, respectively.
  • FIG. 8A shows an example of the progress screen 42 displayed when the weighing of the medicine A is completed in the medicine name display mode.
  • the progress screen 42 shown in FIG. 8A among the drug names displayed in the drug name display unit 401, drug names that have already been weighed are displayed in different colors or highlights.
  • FIG. 8B shows an example of the progress screen 42 displayed when the weighing of the medicine A is completed in the medicine name non-display mode.
  • the progress screen 42 shown in FIG. 8B only the names of medicines that have already been weighed are displayed.
  • the progress screen 42 shown in FIGS. 8 (A) and 8 (B) displays a completion key 421 operated to complete the weighing relating to the prescription information.
  • the completion key 421 embodied on the touch panel 13 is an operation unit for inputting completion of weighing for each prescription information, and is an example of a second input unit according to the present invention.
  • step S ⁇ b> 9 the control unit 11 writes the prescription information and the weighing result (an example of weighing drug information) in the RFID tag 31 by the RFID reader / writer 14.
  • the said control part 11 when performing the process which concerns here corresponds to a recording means.
  • the prescription information includes prescription delivery date, patient ID, patient name, patient birth date, dosage form information (internal use, topical use, etc.), drug information (drug code, drug name, dose), usage information ( Information recorded on the prescription, such as after meals three times a day).
  • the weighing result includes a drug name to be weighed, a weighing target value, an actual weighing value, a matching result between the prescription drug name and the contained drug name, and the like.
  • control unit 11 may record only a part of the prescription information in the RFID tag 31 in step S9.
  • the control unit 11 may store at least the drug name to be weighed in the RFID tag 31.
  • the medicine weighing device 10 and the medicine packaging device 20 are connected so as to be able to communicate with each other via a communication network such as a LAN or the Internet, and the control unit 11 stores information not recorded on the RFID 31 in the medicine packaging. Transmission to the device 20 is conceivable.
  • Step 8 and Step S9 may be executed in reverse order or substantially in parallel. That is, immediately after it is determined that the weighing is completed in step S7, the prescription information and the weighing result may be recorded in the RFID tag 31 in step S9.
  • step S ⁇ b> 10 the control unit 11 determines whether or not the next medicine name has been read by the barcode reader 17.
  • the control part 11 judges that the next accommodation chemical
  • the control part 11 makes a process transfer to step S11, when the next chemical
  • step S11 the control unit 11 determines whether all weighings corresponding to the prescription information have been completed. Specifically, the control unit 11 performs the operation when the completion key 421 displayed on the progress screen 42 is operated as shown in FIGS. 8A and 8B or all of the prescription information included in the prescription information. When the weighing of the weighing target drug is completed, it is determined that all the weighings related to the prescription information are completed.
  • control part 11 will transfer a process to step S12, if it judges that all the weighings regarding the said prescription information were completed (Yes side of S11). On the other hand, the control part 11 makes a process transfer to said step S10, when all the weighings regarding the said prescription information are not completed (No side of S11).
  • the control unit 11 determines that the operation of the completion key 421 has been performed in the step S11, the prescription information included in the prescription information in which the completion of the weighing is input by the operation of the completion key 421. If there is a prescription drug name for which the completion of weighing is not input by the determination key 411 in the drug name, it is possible to display that on the touch panel 13. Thereby, it is possible to warn the user that the weighing is forgotten.
  • the control unit 11 determines whether or not the weighing of each prescription drug name is completed according to the information stored in the RAM in step 7.
  • the said control part 11 when performing the display process which concerns here corresponds to an incomplete display means. Moreover, the said control part 11 may display the said display with a character, an image, an audio
  • the prescription information includes medicines such as external medicines, liquid medicines, tablets, and heat agents (packed with a predetermined amount of powder or tablets) that are not to be weighed by the medicine weighing device 10.
  • medicines such as external medicines, liquid medicines, tablets, and heat agents (packed with a predetermined amount of powder or tablets) that are not to be weighed by the medicine weighing device 10.
  • the medicine weighing apparatus 10 since it is normal for the medicine weighing apparatus 10 not to weigh the medicines not to be weighed, the user is not warned of forgetting to weigh.
  • the control unit 11 displays the warning only when the prescription drug name is powder. Conceivable. This is because powder is highly likely to be measured by the drug weighing device 10 and the user is likely to forget to weigh.
  • the control unit 11 can not perform the warning display when the weighing related to the prescription drug name corresponding to the medicine type not to be weighed is not completed. Thereby, warning display is performed only when necessary, and unnecessary warning display can be prevented.
  • a configuration in which the drug type to be weighed is previously stored in the data storage unit 15 instead of the drug type not to be weighed by the drug weighing device 10 is also conceivable.
  • the method of displaying a warning about forgetting weighing can be arbitrarily switched according to the operation input of the touch panel 13 according to the initial setting screen related to the medicine weighing program displayed by the control unit 11. Conceivable.
  • control unit 11 automatically determines the completion of the weighing related to the prescription information in the step S11. This saves the user from having to operate the completion key 421.
  • control unit 11 determines that the weighing for the previous prescription information has been completed on the condition that the next prescription information has been read. That is, the control unit 11 determines that the weighing related to the prescription information read immediately before is completed on the condition that the two-dimensional code of the prescription is read by the barcode reader 17.
  • control unit 11 determines that the weighing for the prescription information has been completed on the condition that it has been determined that the weighing of all the prescription drug names included in the prescription information has been completed.
  • all the prescription drug names included in the prescription information are drugs to be weighed by the drug weighing device 10, it is possible to automatically determine that the weighing corresponding to the prescription information has been completed. It is.
  • the prescription information includes a medicine that is not to be weighed by the medicine weighing device 10
  • the said control part 11 is the said prescription on the conditions that the measurement of the prescription medicine name which does not correspond to the said chemical
  • a configuration in which the drug type to be weighed in advance is stored in the data storage unit 15 instead of the drug type not to be weighed in the drug weighing device 10 is also conceivable.
  • Step S12> When all the weighings related to the prescription information are completed, the control unit 11 causes the printer 18 to print the prescription information and the weighing result in the subsequent step S12. At this time, the control unit 11 causes only the preset information out of the prescription information and the weighing result to be printed according to a preset layout.
  • the control unit 11 causes the printer 18 to print only the records relating to the drugs weighed in the drug weighing device 10.
  • the prescription information and the weighing result are recorded on the RFID tag 31, so that it is not necessary to perform printing by the printer 18 every time prescription medicine is weighed, and the weighing relating to the prescription information can be performed.
  • the weighing result may be printed when it is completed.
  • the control unit 11 causes the printer 18 to print the weighing result each time the prescription drug is weighed.
  • Step S13 On the other hand, in the step S4, when the stored medicine name read in the step S3 does not correspond to any of the prescription medicine names (No side of S4), the control unit 11 executes the processing after step S13. .
  • step S13 the control unit 11 determines whether or not the stored medicine name is registered in the medicine master stored in the data storage unit 15.
  • the control unit 11 shifts the process to step S14.
  • the control unit 11 shifts the process to step S15.
  • step S14 the control unit 11 displays a warning screen 43 indicating that the medicine is different on the touch panel 13, and returns the process to step S3. Thereby, it can warn a user that selection of a medicine bottle is wrong, and prescription of the wrong medicine can be prevented.
  • the warning is not limited to the display of characters and images on the touch panel 13.
  • the medicine weighing device 10 may have a speaker, and the control unit 11 may display that the medicine is different depending on the speaker.
  • medicine weighing apparatus 10 may have LED for warning display, and the said control part 11 may display that the chemical
  • step S ⁇ b> the control unit 11 determines whether the stored medicine name corresponds to one of the generic drug names stored in the data storage unit 15.
  • the control unit 11 shifts the process to step S16.
  • the control unit 11 shifts the process to step S19.
  • step S ⁇ b> 16 the control unit 11 determines whether the original drug name corresponding to the generic drug name that matches the contained drug name corresponds to any of the prescription drug names. That is, in step S16, the control unit 11 determines whether or not the medicine with the stored medicine name is a generic medicine corresponding to the medicine with the prescription medicine name.
  • control unit 11 shifts the process to step S17.
  • control unit 11 shifts the process to step S19.
  • step S15 it is determined whether the contained medicine name corresponds to either the name of the original medicine or the name of the generic medicine.
  • step S16 the name of the corresponding original medicine name or generic name is determined. It may be considered as another embodiment to determine whether the corresponding generic drug name or the generic drug name corresponds to one of the prescription drug names.
  • step S ⁇ b> 17 the control unit 11 displays a confirmation screen 44 indicating that the medicine with the generic drug name is used.
  • FIG. 9B shows an example of the confirmation screen 44.
  • the confirmation screen 44 displays that the medicine with the contained medicine name is a generic drug and an inquiry as to whether or not to approve the use of the generic drug.
  • the confirmation screen 44 displays an approval key 441 that is operated when the use of the generic drug is approved, and a cancel key 442 that is operated when the use of the generic drug is not approved.
  • step S18 the control unit 11 determines whether the use of the generic drug has been approved. Specifically, the control unit 11 determines which of the approval key 441 or the cancel key 442 is selected in the step S18.
  • the control unit 11 determines that the use of the generic drug has not been approved (No in S18), and shifts the processing to the step S3.
  • the control unit 11 determines that the use of the generic drug has been approved (Yes side of S18), and shifts the processing to the step S5. Thereby, the said control part 11 selects the said prescription drug name corresponding to the said generic drug name among the prescription drug names contained in the said prescription information in the said step S5 as a weighing object, In the said step S6, the said The weighing screen 41 showing the name of the generic drug and the weighing target value is displayed on the touch panel 13.
  • the control unit 11 determines the prescription amount of the generic drug name based on the generic drug master. It is conceivable to calculate the prescription amount of the corresponding generic drug name as the weighing target value.
  • Step S19> On the other hand, when the stored medicine name does not correspond to either the prescription drug name or the generic drug name (No side of S4, No side of S15), the control unit 11 executes the processing after step S19. In addition, even when the original drug name corresponding to the generic drug name that matches the contained drug name does not correspond to any of the prescription drug names (No side of S16), the control unit 11 performs steps S19 and after. Execute the process.
  • the control unit 11 causes the touch panel 13 to display a warning screen 45 indicating that the medicine is different. Thereby, it can warn a user that selection of a medicine bottle is wrong, and prescription of the wrong medicine can be prevented.
  • the warning is not limited to the display of characters and images on the touch panel 13.
  • the medicine weighing device 10 may have a speaker, and the control unit 11 may display that the medicine is different depending on the speaker.
  • medicine weighing apparatus 10 may have LED for warning display, and the said control part 11 may display that the chemical
  • FIG. 9C shows an example of the warning screen 45.
  • the warning screen 45 displays that the medicine is different and an inquiry as to whether or not to register the generic drug name.
  • the warning screen 45 displays a generic drug registration key 451 that is operated when generic drug registration is performed and a cancel key 452 that is operated when generic drug registration is not performed.
  • step S20 the control unit 11 determines whether or not an operation for performing the generic drug registration has been performed. Specifically, the control unit 11 determines which of the generic drug registration key 451 or the cancel key 452 is selected in the step S20.
  • step S3 when the cancel key 452 is operated, the control unit 11 determines that the generic drug registration is not performed (No side of S20), and the process proceeds to step S3.
  • the control unit 11 determines that the generic drug registration is to be performed (Yes side of S20), and the process proceeds to step S21.
  • step S21 the control unit 11 executes a process for editing the generic drug master.
  • the control unit 11 displays a registration screen 51 for registering the generic drug name in the generic drug master on the touch panel 13, and the generic drug according to an operation input according to the display of the registration screen 51. Register a name.
  • the control unit 11 corrects the correspondence between the name of the generic drug and the generic drug name in the generic drug master that has already been registered according to the operation input by the user of the touch panel 13.
  • FIGS. 10A and 10B show an example of the registration screen 51.
  • items such as a medicine code, a medicine name, a classification, a specific gravity, a medicine type, a compounding change, a shaping medicine, a unit, and a weighing can be set.
  • the control unit 11 registers the generic drug name in the generic drug master according to the operation of the registration key 511, and closes the registration screen 51 according to the operation of the return key 512. Further, the control unit 11 switches the display content of the registration screen 51 in accordance with the operation of the previous page key 513 or the next page key 514.
  • the control unit 11 changes the setting items on the registration screen 51 to the name of the original medicine, JAN code, and vial code. Change to In FIG. 10B, a JAN capture key 515 and a normal dose key 516 are displayed.
  • the control unit 11 takes in the JAN code from the bar code attached to the medicine bottle by the bar code reader 17 according to the operation of the JAN take-in key 515. Further, the control unit 11 opens a normal dose setting screen for setting a normal dose corresponding to the generic drug name in accordance with the operation of the normal dose key 516, and uses the normal dose setting screen according to the input of the normal dose setting screen. Set the amount.
  • the normal dose is an amount that can be expected to have a therapeutic effect when the drug is most commonly used.
  • the control unit 11 shifts the processing to step S15. That is, the user can temporarily resume the weighing operation related to the prescription information as it is after temporarily suspending the weighing operation related to the prescription information and editing the generic drug master. Therefore, the user can appropriately edit the generic drug master and enrich its contents during daily operation using the drug weighing device 10.
  • the weighing work (medicine weighing process) based on the prescription information is temporarily ended and the generic drug master is edited on the initial setting screen or the like, the weighing work based on the prescription information (medicine weighing process) is thereafter performed. ) From the beginning, the user is forced to perform complicated work.
  • the user who uses the drug weighing device 10 allows the barcode reader 17 to sequentially read the two-dimensional code of the prescription and the barcode of the medicine bottle, so that the drug according to the prescription can be accurately and easily. Weighing can be performed.
  • the medicine weighing apparatus 10 checks the name of the medicine to be stored and the name of the prescription medicine, and the weighing target to be weighed from now is started. A prescription drug name is selected. Therefore, when a plurality of prescription drug names are recorded in the prescription, the user can save the trouble of selecting the prescription drug name to be weighed.
  • step S31 the control unit 21 determines whether or not prescription information is input. Specifically, the control unit 21 determines whether prescription information has been read from the RFID tag 31 by the RFID reader / writer 24. In this way, in the medicine weighing system 1, since the prescription information can be read from the RFID tag 31 in the medicine packaging apparatus 20, the medicine packaging apparatus 20 is communicably connected to a host system such as a dispensing support system. There is no need to do. In addition, since the prescription information is acquired from the RFID tag 31 in the medicine packaging device 20, the prescription information input operation in the medicine packaging device 20 and the medicine packaging device 20 that have been conventionally performed by a user are operated. Can reduce the operation work.
  • the medicine packaging device 20 is communicably connected to the host system.
  • the control unit 21 determines whether or not the prescription information is input from the host system in the step S31.
  • a configuration in which the control unit 21 includes a barcode reader that reads prescription information from a two-dimensional code recorded in a prescription is also conceivable as another embodiment.
  • the control unit 21 determines whether or not the two-dimensional code is read in the step S31.
  • the medicine packaging apparatus 20 has a plurality of input functions for inputting the prescription information by these different methods, and a configuration in which any one of the input functions can be selected in advance is also conceivable.
  • step S32 when the control unit 21 determines that the prescription information has been input (Yes side of S31), the process proceeds to step S32, and when the control unit 21 determines that the prescription information has not been input (S31). No side), the process proceeds to step S33.
  • step S32 the control unit 21 selects which one of the hopper 25A and the hopper 25B is used in the medicine packaging related to the prescription information read in step S31.
  • the hopper 25A is used for packaging the medicine, and when prescription information describing a medicine prescribed for the patient C2 is input. It is possible that the hopper 25B is used in advance for the packaging of the medicine, and the prescription information includes allocation information indicating that fact. In this case, in step S32, the control unit 21 can determine whether to use the hopper 25A or the hopper 25B according to the allocation information included in the prescription information.
  • control unit 21 automatically assigns which one of the hopper 25A and the hopper 25B is used for each prescription information in the step S32. Is also possible. For example, the control unit 21 may select to use the hopper 25A and the hopper 25B alternately each time the prescription information is input.
  • the user can use the hopper 25A and the hopper 25B separately for each prescription information so that the medicine can be put into the medicine. Can proceed in parallel.
  • step S ⁇ b> 33 the control unit 21 determines whether or not the medicine name of the medicine placed on the medicine sheet 30 (hereinafter referred to as “injected medicine name”) has been read from the RFID tag 31.
  • step S31 when the prescription information is read from the RFID tag 31, the input medicine name is also read at the same time. Therefore, in step 33, it is determined that the input medicine name has been read.
  • Step S34 when the input medicine name is read (Yes side of S33), the control unit 21 shifts the process to Step S34, and until the input medicine name is read (No side of S33), The process proceeds to step S31.
  • step S34 the control unit 21 selects whether to use the hopper 25A or the hopper 25B based on the prescription information and the input medicine name. For example, in step S32, it is assumed that the hopper 25A is used for packaging the medicine prescribed for the patient C1, and the hopper 25B is used for packaging the medicine prescribed for the patient C2. In this case, in step S34, when the input medicine name included in the prescription information corresponding to the patient C1 is read, the hopper 25A is selected, and the input medicine name included in the prescription information corresponding to the patient C2 is read. And the hopper 25B is selected.
  • the prescription information input from the host system or the prescription information read from the two-dimensional code of the prescription is used. Whether to use the hopper 25A or the hopper 25B is selected. Therefore, if the RFID tag 31 stores at least information such as a medicine name and a weighing value related to the medicine placed on the medicine sheet 30, the control unit 21 performs the process in step S34 based on the information. Judgment can be made. Specifically, the control unit 21 specifies prescription information including a prescription medicine name and a prescription amount corresponding to a medicine name and a weighing value related to the medicine placed on the medicine sheet 30, and corresponds to the prescription information. Either the hopper 25A or the hopper 25B to be selected is selected.
  • step S35 the control unit 21 causes the touch panel 23 to display the selection result in step S34 as characters or images.
  • the control unit 21 performs a guidance display such as “Please insert A medicine into the A hopper”.
  • the display is performed to notify the user of either the hopper 25A or the hopper 25B, and is not limited to the display on the touch panel 23.
  • control unit 21 may display the selection result by voice. It is also conceivable that an LED or the like is provided in each of the hopper 25A and the hopper 25B, and the selection result is displayed by the controller 21 lighting one of the LEDs. Further, if the inlets of the hopper 25A and the hopper 25B can be opened and closed by a predetermined driving means, the control unit 21 controls the driving means to determine which of the inlets of the hopper 25A and the hopper 25B. It is also conceivable to display the selection result by opening the button.
  • the hopper 25A and the hopper 25B are each provided with a locking means for restricting the opening of the charging opening, and the control unit 21 releases only one of the locking means and removes the other. It is also conceivable that, by setting the lock state, the user can open only the charging port into which the drug on the drug sheet 30 should be charged.
  • the medicine packaging device 20 the medicine is charged based on the information stored in the RFID tag 31 provided on the medicine sheet 30 inseparable from the medicine weighed by the medicine weighing device 10.
  • the destination is automatically displayed. Therefore, the user can easily grasp the place where the medicine is placed, and an error in the place where the medicine is placed can be prevented.
  • a notification method of the selection result in step S34 if any two or more of various notification methods such as display on the touch panel 23, the voice display, and the LED display are used in combination, the user inputs the medicine. Can be more effectively prevented.
  • step S36 the control unit 21 controls the packaging operation performed by the packaging unit 22 according to preset control conditions based on the prescription information and the weighing result read from the RFID 31. .
  • the said control part 21 when performing the process which concerns here corresponds to a packaging control means.
  • step S36 control of different packaging operations can be executed based on the prescription information and the weighing result.
  • medicine packaging is performed under conditions suitable for each medicine. Can do.
  • the control unit 21 is preset for each type of powder according to the prescription information read from the RFID tag 31 as the weighing drug information and the type of medicine included in the weighing result.
  • An operation is performed by the dividing unit or the packaging unit.
  • control unit 21 prevents the scattering by slowing the packaging speed (such as the rotation speed of the annular distribution dish in the dividing unit 221) when packaging the type of powder that is likely to be scattered.
  • packaging speed such as the rotation speed of the annular distribution dish in the dividing unit 221
  • steps S311 to S312 described later are executed by the control unit 21 between the step S31 and the step S32 shown in FIG. .
  • step S311 the control unit 21 determines whether or not a plurality of prescription drug names are included in the prescription information input in step S31. Here, if the control unit 21 determines that a plurality of prescription drug names are included (Yes in S311), the process proceeds to step S312 and determines that a plurality of prescription drug names are not included ( (No side of S311), the process proceeds to step S32.
  • the control unit 21 selects which of the hopper 25A and the hopper 25B is used for each prescription drug name included in the prescription information.
  • the prescription information includes allocation information regarding which of the hopper 25A or the hopper 25B is used for each prescription drug name, and the control unit 21 includes the prescription information. It is conceivable to determine which one of the hopper 25A or the hopper 25B is used according to the allocation information included. Specifically, it is conceivable that which one of the hopper 25A or the hopper 25B is used for each medicine color (red, white, etc.) is predetermined for each medical facility or pharmacy.
  • the hopper 25A and the hopper 25B are selectively used for a colored chemical with color and a colorless chemical without color.
  • the control unit 21 automatically uses the hopper 25A or the hopper 25B for each prescription drug name, such as alternately using the hopper 25A and the hopper 25B for each prescription drug name. It is also possible to assign to
  • the control unit 21 when there are two prescription drug names predetermined as medicines to be accommodated in the same wrapping paper among a plurality of prescription medicine names, the control unit 21 The user selects to use the hopper 25A on the one hand and the hopper 25B on the other hand. Thereby, in the medicine packaging operation by the packaging unit 22 of the medicine packaging apparatus 20 in the step S36, the prescription medicines put into the hopper 25A and the hopper 25B are packaged in the same wrapping paper in one dose unit. Can be made. For example, when two types (a plurality of types) of medicines with different dosing times are included in one prescription information, the medicine packaging device 20 operates as follows.
  • the control unit 21 refers to the prescription information from the prescription information, and each of the powder M1, M2 is taken, and the powder M1 and the powder M2 are “the morning of the powder M1”. And the morning of the powder M2, the day of the powder M1, and the evening of the powder M1 and the evening of the powder M2 are packaged in the same wrapping paper.
  • This is a function that can be realized when the control unit 21 refers to the medication time of each medicine from the prescription information recorded in the RFID tag 31.
  • the medicine packaging device 20 since the prescription information is acquired from the RFID tag 31, the prescription information input operation in the medicine packaging device 20 and the medicine packaging device 20 which are conventionally performed by the user are operated. The operation work for reducing is reduced.
  • the hopper 25A and the hopper 25B for each prescription drug name can be used properly, and dispensing of a plurality of prescription drugs can proceed in parallel.
  • the prescription drugs can be packaged in the same wrapping paper in single dose units using the hoppers 25A and 25B at the same time.
  • control unit 21 performs the steps S32 and S312 in the medicine packaging process according to the first modified example shown in FIG. Steps S313 to S315 described later are executed.
  • step S313 the control unit 21 determines whether there is unfinished prescription information in which the medicine packaging operation executed in step S36 is not completed for all medicines.
  • the process proceeds to step S314, and when the incomplete prescription information does not exist (S313) No side), the process proceeds to step S33.
  • step S314 the control unit 21 determines whether or not a hopper used in the medicine packaging operation related to the incomplete prescription information has been selected. In addition, when only calling it a "hopper", either one or both of the said hoppers 25A and 25B are shown. When the hopper used in the medicine packaging operation related to the incomplete prescription information or the hopper to be used is not selected (No in S314), the control unit 21 proceeds to step S33. Let Thereby, for example, when there is no medicine to be packed with the same wrapping paper in the incomplete prescription information, or when there is only one remaining medicine, both the hopper 25A and the hopper 25B are used. When it is not necessary, the hopper 25A and the hopper 25B can be used in a medicine dispensing operation described in different prescription information.
  • step S315 if it is determined that the hopper used in the medicine packaging operation related to the incomplete prescription information or the hopper to be used is selected (Yes in S314), the process proceeds to step S315.
  • step S315 the control unit 21 causes the process to wait until the medicine packaging operation related to the incomplete prescription information is completed, and then shifts the process to step S33. In this case, it is conceivable that the control unit 21 displays an error for notifying the user that there is no usable hopper using characters, images, sounds, light, or the like.
  • the hopper 25A and the hopper 25B when there is a need to use both the hopper 25A and the hopper 25B, for example, when there is a medicine to be packed with the same wrapping paper in the incomplete prescription information, it is described in the other prescription information. It is possible to prohibit the use of the hopper 25A and the hopper 25B in the medicine packaging operation relating to the finished medicine. In addition, when there are two or more remaining medicines included in the incomplete prescription information, the next prescription information is prevented from being interrupted, so that the prescription information can be processed sequentially, thereby preventing dispensing errors. can do.
  • the medicine packaging device 20 in which the medicine packaging processing according to the third modification is executed is performed by the individual RFID reader / writers 24 provided at positions corresponding to the plurality of the hoppers 25A and the hoppers 25B, respectively. It is necessary to have.
  • the RFID reader / writer 24 provided at a position corresponding to the hopper 25A is referred to as an RFID reader / writer 24A
  • the RFID reader / writer 24 provided at a position corresponding to the hopper 25B is referred to as an RFID reader / writer 24B.
  • the RFID reader / writer 24A is placed near the loading port of the hopper 25A, and a mounting table (for example, the lid of the loading port) of the medicine sheet 30, and the RFID reader / writer 24B is mounted on the hopper 25B. It arrange
  • step S341 the control unit 21 determines whether or not the hopper to which the user is going to put the medicine on the medicine sheet 30 is correct.
  • control unit 21 determines whether the user inputs the medicine on the medicine sheet 30 depending on whether the RFID reader / writer 24 or the RFID reader / writer 24B reads the input medicine name from the RFID tag 31. Determine the hopper you are trying to load. Then, the control unit 21 determines whether the hopper 25A or the hopper 25B provided with the RFID reader / writer 24 or the RFID reader / writer 24B which has read the input medicine name is the hopper selected in the step S32. Judge whether or not.
  • control unit 21 determines that the hopper to which the medicine of the medicine sheet 30 is to be loaded is correct (Yes in S341), the control unit 21 shifts the process to step S342 and determines that the hopper is not correct (S341). No side), the process proceeds to step S343.
  • step S342 the control unit 21 notifies the user that the hopper to which the medicine in the medicine sheet 30 is to be put is correct. Specifically, it is conceivable that the control unit 21 displays that fact on the touch panel 23. In addition, the control unit 21 may turn on the LEDs and the like provided in the hopper 25A and the hopper 25B with a predetermined color (blue or green) corresponding to the case where the hopper is correct. Of course, it can be considered that the hopper is correct by voice. Further, the control unit 21 may automatically open the hopper input port or unlock the hopper input port only when the hopper to which the drug of the drug sheet 30 is to be input is correct. Conceivable.
  • step S343 the control unit 21 notifies the user that the hopper trying to put the medicine in the medicine sheet 30 is incorrect. Specifically, it is conceivable that the control unit 21 displays that fact on the touch panel 23. In addition, the control unit 21 may turn on the LEDs and the like provided in the hopper 25A and the hopper 25B with a predetermined color (red or the like) corresponding to a case where the hopper is incorrect. Of course, it may be possible to indicate that the hopper is wrong by voice or the like.
  • the user places the medicine sheet 30 on the position where the RFID reader / writer 24A or the RFID reader / writer 24B is provided, thereby the medicine sheet 30. Therefore, it is possible to effectively check whether or not a medicine is placed on the medicine sheet 30.
  • the third modified example executes steps S341 to S343 instead of the steps S34 to S35 in the medicine packaging process (see FIGS. 12 and 13) according to the first modified example and the second modified example. It is also possible. Thereby, for example, when a plurality of medicines are included in the prescription information, the user determines whether or not the medicine input destination of the medicine sheet 30 is appropriate as the hopper selected for each medicine (S312). Can be easily confirmed.
  • the medicine weighing device 10 can arbitrarily select an input mode of the prescription information.
  • the control unit 11 causes the touch panel 13 to display an initial setting screen related to the medicine weighing program, and selects the input mode according to an operation input performed according to the initial setting screen.
  • the input mode includes a barcode reading mode for reading the prescription information using the bar code reader 17, a manual input mode for manually inputting the prescription information using the touch panel 13, and a host system of the medicine weighing apparatus 10.
  • medicine weighing apparatus 10 has the said network input mode
  • medicine weighing apparatus 10 has a communication interface which communicates between host systems, such as a dispensing assistance system, via communication networks, such as LAN or the internet.
  • the said control part 11 performs the process procedure similar to the said chemical
  • the reading of prescription information from the prescription in step S1 merely replaces the input of prescription information from the host system.
  • the control unit 11 automatically reads the barcode reading on the condition that the barcode reader 17 reads the two-dimensional code. It is possible to switch to the mode.
  • the medicine weighing device 10 includes a microphone for inputting voice and a voice recognition means for executing voice recognition processing for inputting information according to the voice input to the microphone is also conceivable.
  • the voice recognition means is, for example, the control unit 11 when executing the voice recognition process.
  • the dispensing unit or the like reads out the content of the prescription printed on paper or the handwritten prescription aloud, so that the control unit 11 reads the prescription information recorded in the prescription. 10 can be entered. That is, it is conceivable that the medicine weighing device 10 has a voice input mode for inputting the prescription information by voice as the input mode.
  • the control unit 11 reads out the prescription information recorded in the prescription collectively and inputs information related to a plurality of drug names to the drug weighing device 10 and then a plurality of prescription information according to the prescription information. It is conceivable to continuously carry out weighings relating to drug names. In addition, the control unit 11 may execute weighing for a medicine name every time one medicine name is read out of the prescription information recorded in the prescription.
  • the medicine weighing process (see FIG. 5) is a processing procedure when reading prescription information from one prescription and sequentially weighing each prescription drug name included in the prescription information.
  • the medicine weighing device 10 has a prescription batch reading mode in which prescription information can be continuously read from a plurality of prescriptions and the weighing of each prescription information can be advanced in parallel.
  • the prescription batch reading mode is implemented when the control unit 11 executes the medicine weighing program.
  • FIG. 15A shows prescription information read from a plurality of prescriptions D1 to D3.
  • the prescription D1 contains medicines A to C
  • the prescription D2 contains medicines D to F
  • the prescription D3 contains medicines G to I.
  • step S4 the control unit 11 determines whether the contained medicine name is one of the prescription medicine names of the plurality of prescription information. It is judged whether it corresponds to. Specifically, after the prescriptions D1 to D3 shown in FIG. 15A are read and “medicine E” is read as the contained medicine name (Yes side of S3), the prescription D2 contains “ Since “medicine E” is included (Yes side of S4), the process proceeds to step S5. In step S5, the medicine E included in the prescription information corresponding to the prescription D2 is automatically selected as a weighing target (S5), and the prescription amount of the medicine E recorded in the prescription D2 is displayed on the weighing screen. 41 is displayed (S6).
  • the contained medicine name corresponds to a prescription medicine name included in a plurality of the prescription information. Therefore, in such a case, the control unit 11 may allow the user to arbitrarily select any prescription information.
  • FIG. 15B shows another example of prescription information read from a plurality of prescriptions D1 to D3.
  • the prescription D1 includes medicines A to C
  • the prescription D2 includes medicines D to F
  • the prescription D3 includes medicines E, H, and I. That is, the medicine E is contained in each of the prescriptions D2 and D3.
  • a prescription selection screen 61 for selecting one of the prescriptions D3 is displayed on the touch panel 13.
  • FIG. 15C shows an example of the prescription selection screen 61.
  • the said control part 11 selects "the medicine E" of the said prescription D2 or the said prescription D3 selected on the said prescription selection screen 61 as a weighing object (S5), and the prescription amount of the medicine E recorded on the prescription Is displayed on the weighing screen 41 (S6).
  • a plurality of prescriptions can be continuously read by the barcode reader 17, and then the weighing of each medicine recorded in the prescription can be continuously advanced. Dispensing efficiency can be increased.
  • medicines may be weighed according to a plurality of prescriptions prescribed for each department. Also in this case, as described above, it is preferable to read the prescription information continuously from a plurality of prescriptions. Thereby, after letting the barcode reader 17 read a plurality of prescriptions continuously, the weighing of each medicine recorded on the prescription can be continuously advanced, and the dispensing efficiency of the user can be improved. .
  • the control unit 11 displays a pop-up screen for arbitrarily selecting whether or not to integrate those prescriptions as one prescription information. Can be displayed.
  • the control unit 11 generates one prescription information from a plurality of prescription information read from the plurality of prescriptions when it is selected to integrate a plurality of prescriptions into one prescription information according to the pop-up screen. Thereafter, weighing is performed in the drug weighing device 10 in accordance with the generated prescription information after integration.
  • control unit 11 can acquire all prescription drug names recorded in each prescription by continuously reading a plurality of prescriptions of the same patient. Therefore, when the plurality of prescriptions of the same patient are read, the control unit 11 has a medicine that is prohibited in advance from being taken at the same time among all the prescription medicine names recorded in each of the prescriptions. It may be possible to determine whether or not there is any. For example, the medicines that are prohibited from being taken at the same time are predetermined as a plurality of medicines that cause compounding changes and side effects. At this time, the control unit 11 audits whether or not a plurality of medicines included in each of the prescription information are prohibited from being taken at the same time. Based on prohibited information.
  • the control unit 11 displays a warning to that effect on the touch panel 13 or the like. It is possible.
  • medical agent which a mixing
  • the drug weighing system 2 includes one or more drug weighing devices 10, one or more drug packaging devices 20, and a host system 70 connected to each of the drug weighing devices 10. Is provided.
  • the drug weighing device 10, the drug packaging device 20, and the host system 70 are communicably connected via a network N such as a LAN or the Internet.
  • the control unit 11 of the chemical weighing apparatus 10 includes a CPU 111, an SD card 112, and a RAM 113.
  • the SD card 112 is a storage unit that stores various programs such as a kernel 114, an OS 115, and a scale unit application 116 executed by the CPU 111.
  • a storage means such as a ROM storing the various programs may be provided.
  • the kernel 114 is a software program such as Linux (registered trademark)
  • the OS 115 is an operating system such as Android (registered trademark) or iOS (registered trademark).
  • the scale single unit application is a software program for operating the chemical weighing apparatus 10 as a normal electronic balance.
  • the control unit 11 incorporated in the chemical weighing apparatus 10 executes various processes such as the chemical weighing process (see FIG. 5) executed by the chemical weighing apparatus 10. No program or database is stored. Therefore, in the chemical weighing apparatus 10, the function stability as an electronic balance is ensured.
  • the data storage unit 15 detachable from the USB port 16 is a USB memory for storing a log 151, a setting file 152, a form layout file 153, a medicine weighing program 154, a database 155, a database dump file 156, and the like.
  • the log 151 is log data indicating a history of operations of the chemical weighing device 10. It is also conceivable that a card slot is provided in place of the USB port 16 and the data storage unit 15 is a recording medium such as an SD card.
  • the setting file 152 and the form layout file 153 are data including setting contents of various processes executed by the control unit 11 or a print form.
  • the chemical weighing program 154 is a software program for causing the control unit 11 to execute various processes such as the chemical weighing process (see FIG. 5).
  • the database 155 stores various master data, prescription information, weighing results, and the like used in the drug weighing process in a database format.
  • the database dump file 156 is a backup file output from the database 155 in a startup process (see FIG. 39) described later. The database dump file 156 is used to restore data at the time of backup when an abnormality occurs in some or all of various data stored in the database 156.
  • the medicine packaging apparatus 20 includes a data storage unit 26 such as a hard disk or an SSD, and a printing unit 27 that prints information on a wrapping paper used for packaging the medicine in the packaging unit 22.
  • the data storage unit 26 is provided with a shared folder that can be accessed from each of the drug weighing devices 10 via the network N.
  • the control unit 11 includes the prescription information, the weighing result, and a tray number described later assigned to the dispensing sheet 30 in the shared folder of the data storage unit 26. Information can be stored.
  • the control unit 11 stores the prescription information and the weighing result in the data storage unit 26 in association with the tray number.
  • the control unit 21 reads the tray number from the RFID tag 31 of the medicine sheet 30 and stores the prescription information and the weighing result corresponding to the medicine sheet 30 based on the tray number in the data storage. It is possible to read from the unit 26.
  • the host system 70 is, for example, an electronic medical record system or a dispensing support system, and is an information processing apparatus such as a personal computer that inputs and manages the prescription information related to prescription drugs to be prescribed to a patient.
  • the host system 70 includes a control unit 71, a data storage unit 72, and the like.
  • the control unit 71 includes a CPU, a RAM, a ROM, and the like, and controls the host system 70 in an integrated manner.
  • the data storage unit 72 is a non-volatile storage unit such as a hard disk or an SSD that stores a program for causing the control unit 71 to execute various processes and the prescription information.
  • the control unit 71 can transmit the prescription information stored in the data storage unit 72 to the drug weighing device 10 in response to a transmission request from the drug weighing device 10. .
  • the control unit 71 locks the prescription information selected as a weighing target in any one of the drug weighing devices 10 and performs exclusive processing so that the same prescription information is not selected in the other drug weighing devices. Execute. Thereby, duplication of the weighing operation based on the drug weighing information using the plurality of drug weighing devices 10 is prevented.
  • the control unit 71 can also transmit the prescription information to the medicine packaging device 20 in response to a transmission request from the medicine packaging device 20. In addition, the control unit 71 can actively transmit the prescription information to the medicine weighing device 10 or the medicine packaging device 20.
  • the drug weighing device 10 reads the prescription information from the prescription by the barcode reader 17 and inputs the prescription information to the touch panel 13, and the prescription information from the host system 70. Information can be acquired.
  • the control unit 11 stores the prescription information in the data storage unit 15. Thereby, the control unit 11 can read the prescription information arbitrarily selected from the data storage unit 15 in response to a user operation on the touch panel 13. As will be described later, the control unit 11 can also automatically read out the prescription information from the data storage unit 15 in time series. Further, the control unit 11 can access the data storage unit 72 of the host system 70 via the network N, read the prescription information, and copy it to the data storage unit 15.
  • the medicine weighing apparatus 10 when the control unit 11 reads the prescription information from the prescription by the barcode reader 17 or when the prescription information stored in the data storage unit 15 is read.
  • Execute prescription input process is a process executed between Step S1 and Step S2 in the medicine weighing process.
  • the said prescription input process demonstrated here may be performed with the said chemical
  • step S41 the control unit 11 determines whether or not the prescription information is within the expiration date according to the expiration date information included in the prescription information.
  • the control unit 11 shifts the processing to step S411.
  • step S411 the control unit 11 displays on the touch panel 13 that the expiration date has expired and notifies the user that the prescription information has not been preliminarily measured. End.
  • the said control part 11 judges that it is within the said expiration date (Yes side of S41), it will transfer a process to step S42.
  • Steps S42 to S43 the control unit 11 analyzes usage information and medicine information of one or a plurality of recipes included in the prescription information, and acquires information on usage and prescription medicine of each recipe.
  • the said recipe means prescription of a taking unit and is abbreviated as "Rp" at the time of the display or printing in the said chemical weighing system 2.
  • recipe information information on each of the recipes included in the prescription information is referred to as recipe information.
  • step S44 the control unit 11 determines whether or not an unequal record exists in the recipe included in the prescription information.
  • the unequal record is a recipe in which the prescription amount of prescription medicine varies depending on the time of taking. For example, for A medicine, a recipe with prescription amounts of 1 mg, 1 mg, and 2 mg for each morning, noon, and evening time corresponds to the unequal record.
  • the control unit 11 shifts the process to Step S45 and determines that the unequal record does not exist (No side of S44). The process proceeds to step S46.
  • step S ⁇ b> 45 the control unit 11 executes a recipe dividing process for dividing a recipe in which the unequal record exists among recipes included in the prescription information into recipes by taking time units.
  • FIG. 19 shows an example of the recipe Rp1, which is an example of the unequal record, and recipes Rp11 to Rp13 after the recipe division process.
  • the recipe Rp1 the prescription amount of “A medicine” in the morning, noon and evening is different from the prescription amount in the morning and noon. Therefore, as shown in FIG. 19, the control unit 11 divides the recipe Rp1 into a recipe Rp11 corresponding to only morning, a recipe Rp12 corresponding to only daytime, and a recipe Rp13 corresponding to only evening.
  • step S45 whether or not the recipe division process is executed in step S45 can be changed by the control unit 11 according to a user operation on the touch panel 13 in an initial setting of the chemical weighing device 10 or the like.
  • step S46 the control unit 11 determines whether or not there are a plurality of recipes having the same usage and number of days in the prescription information. For example, when there is a recipe that prescribes A medicine for 7 days in the morning and noon and a recipe that prescribes B medicine for 7 days in the morning and noon, It is determined that there are a plurality of recipes having the same number of days.
  • the said control part 11 judges that there exist multiple recipes with the same usage and the number of days (Yes side of S46), it will transfer a process to step S47 and will judge that there is no recipe with the same usage and the number of days. (No side of S46), the process proceeds to step S48.
  • step S ⁇ b> 47 the control unit 11 executes a recipe collecting process for collecting a plurality of recipes having the same usage and the same number of days in the prescription information as one recipe.
  • FIG. 20 shows an example of recipes Rp21 to Rp23 before being collected, and recipes Rp2 and Rp23 after the recipe collecting process. As shown in FIG. 20, among the recipes Rp21 to Rp23, the recipe Rp21 and the recipe Rp22 have the same usage (minute 2) and the number of days (7 days). Therefore, as shown in FIG. 20, the control unit 11 combines the recipe Rp21 and the recipe Rp22 into one recipe Rp2.
  • step S47 the packaging of a plurality of prescription medicines is realized in the packaging process of the medicine packaging device 20 performed based on the prescription information after being collected by the medicine weighing device 10.
  • whether or not the recipe collecting process is executed in step S47 can be changed by the control unit 11 in accordance with a user operation on the touch panel 13 in the initial setting of the chemical weighing device 10 or the like.
  • step S48 the control unit 11 stores the prescription information after the recipe dividing process in the step S45 or the recipe collecting process in the step S47 in the data storage unit 15, and the prescription information is stored in the data storage unit 15.
  • the data is stored in the shared folder of the data storage unit 26 of the medicine packaging device 20. Thereby, also in the said medicine packaging apparatus 20, it is possible to read the said prescription information and to perform a packaging process.
  • the control unit 11 executes display control processing for controlling the screen display of the touch panel 13 in accordance with the type of system interlocking of the medicine weighing device 10 set in advance.
  • the system interlocking selection screen P ⁇ b> 21 for selecting the type of system interlocking is displayed on the touch panel 13 by the control unit 11 in the initial setting or the like.
  • FIG. 21 is a diagram showing an example of the system linkage selection screen P21. As shown in FIG. 21, on the system linkage selection screen P21, the types of the system linkage are “sequential”, “patient ID”, “exchange ticket number”, “unprocessed”, “processed”, and “single”.
  • a plurality of touch keys corresponding to is displayed. Then, the control unit 11 sets the type of system linkage according to a user operation on the touch key of the touch panel 13. When the system interlocking type of the drug weighing device 10 is set to “single”, the control unit 11 makes the drug weighing device 10 usable as an electronic balance and inputs the prescription information. Will not accept.
  • step S51 the control unit 11 determines whether or not the system interlocking type of the medicine weighing device 10 is set to “sequential”.
  • “sequential” is an operation mode in which the control unit 11 displays the recipe of the prescription information acquired from the host system 70 in order on the touch panel 13.
  • the control unit 11 shifts the process to step S52, and if it is not “sequential” (No side of S51), The process proceeds to step S53.
  • step S ⁇ b> 52 the control unit 11 causes the touch panel 13 to display a prescription screen P ⁇ b> 23 for displaying the recipe information to be weighed by the drug weighing device 10.
  • 23 and 24 are diagrams showing an example of the prescription screen P23.
  • the prescription screen P23 includes a prescription information area A231 in which the dispenser, prescription number, number of days, fraction, age, weight, and the like of the recipe information are displayed.
  • the said control part 11 can also input the said recipe information directly according to user operation with respect to each display location of the said prescription information area
  • the prescription screen P23 includes a medicine display area A232 in which the daily amount and the total amount for each prescription medicine to be weighed are displayed. Moreover, the said control part 11 switches the display content of the daily amount and the total amount for every said prescription medicine alternately with the measurement amount and the target amount according to the user's touch operation with respect to the said medicine display area A232.
  • the actually measured amount is a value actually measured by the chemical weighing apparatus 10, and the target amount is a value determined as a prescription amount by the recipe information.
  • a menu key K233 is displayed on the prescription screen P23, and the control unit 11 performs an initial setting for starting the setting of the system linkage type in response to a user operation of the menu key K233. Display the menu screen.
  • the prescription screen P23 includes a development area A234.
  • the control unit 11 expands the display area of the expansion area A234 as shown in FIG.
  • various touch keys indicating the contents that can be operated on the prescription screen P23 are displayed.
  • a setting key K235 for setting the type of packaging paper used in the packaging operation in the medicine packaging device 20 is displayed in the development area A234.
  • the control unit 11 displays a setting screen for setting the type of the wrapping paper in response to a user operation of the setting key K235.
  • the control unit 11 records the type of the packaging paper input on the setting screen as the prescription information referred to during the packaging operation in the medicine packaging device 20.
  • the type of the wrapping paper is distinguished by the material and length of the wrapping paper, and a plurality of combinations for selecting the material and length of the wrapping paper are displayed on the setting screen.
  • step S ⁇ b> 53 the control unit 11 determines whether the system interlocking type of the chemical weighing device 10 is set to “unprocessed” or “processed”. “Unprocessed” is an operation mode in which the control unit 11 displays only the prescription information for which weighing has not been completed by the drug weighing device 10. “Processed” is an operation mode in which the control unit 11 displays only the prescription information for which weighing has been completed by the drug weighing device 10.
  • the control unit 11 shifts the process to step S54, and selects “unprocessed” or “processed”. If it is not “complete” (No in S53), the process proceeds to step S56.
  • step S ⁇ b> 54 the control unit 11 determines whether a prescription unit or a recipe unit is selected as the display format when selecting the weighing target in the initial setting in the drug weighing device 10. If the control unit 11 determines that the prescription unit is selected, the control unit 11 shifts the process to step S551 (Yes in S54), and determines that the recipe unit is selected (No in S54). Side), the process proceeds to step S552.
  • step S551 the control unit 11 causes the touch panel 13 to display a prescription list screen P25 including a list of the prescription information.
  • the prescription list screen P25 displays a list of the prescription information that has not been weighed by the drug weighing device 10 when the type of system linkage is “unprocessed”.
  • a list of the prescription information that has been weighed by the drug weighing device 10 is displayed on the prescription list screen P25.
  • 25 and 26 are diagrams showing an example of the prescription list screen P25. As shown in FIG. 25, items such as patient ID, patient name, medical department, number of recipes (number of Rp), drug name, and deletion corresponding to the prescription information are displayed on the prescription list screen P25. .
  • a development area A251 is displayed on the prescription list screen P25.
  • the control unit 11 expands the display area of the development area A251 as shown in FIG.
  • various touch keys indicating the contents that can be operated on the prescription list screen P25 are displayed.
  • the control unit 11 when displaying the prescription list screen P25, the control unit 11 requests the host system 70 to transmit a predetermined number of prescription information that can be displayed simultaneously on the prescription list screen P25. Then, the control unit 11 receives the predetermined number of the prescription information from the host system 70 and stores it in the data storage unit 15. In this case, the control unit 11 switches the contents of the prescription information displayed on the prescription list screen P25 in accordance with the operation of “previous data” or “next data” displayed in the development area A251. Specifically, in response to an operation of “previous data” displayed in the expansion area A251, the control unit 11 transmits a predetermined number of the prescription information before the prescription information currently displayed. Request to system 70.
  • the control unit 11 transmits a predetermined number of the prescription information after the prescription information currently displayed in response to the operation of “next data” displayed in the development area A251. To request. Accordingly, the control unit 11 stores the predetermined number of the prescription information transmitted from the host system 70 in the data storage unit 15 and displays the prescription information on the prescription list screen P25.
  • the medicine weighing device 10 is configured to obtain only the necessary prescription information from the host system 70, the prescription in a configuration in which a plurality of the drug weighing devices 10 are connected to the host system 70.
  • Information exclusion processing can be realized. Specifically, as described above, in the host system 70, the control unit 71 locks the prescription information selected as the weighing target in one of the drug weighing devices 10, and the other drug weighing device 10 It is conceivable to perform control so as not to transmit to the network.
  • the medicine weighing device 10 acquires the prescription information from the host system 70 in accordance with, for example, a dispensing system prescription IF sharing specification (NSIPS) is also conceivable.
  • the prescription information may be transmitted from the medicine packaging device 20 to the medicine weighing device 10 after being transmitted from the host system 70 to the medicine packaging device 20.
  • the control unit 11 stores the prescription information acquired from the host system 70 or the medicine packaging apparatus 20 in the data storage unit 15.
  • the data storage unit 15 can store not only the predetermined number that can be displayed on the prescription list screen P25 but also a large number of the prescription information.
  • the control unit 11 can slide and change the prescription information displayed on the prescription list screen P25 in accordance with a user's vertical flick operation on the prescription list screen P25.
  • “previous data”, “next data”, and the like are not displayed in the development area A251.
  • the control unit 11 requests the host system 70 to transmit more prescription information than the predetermined number that can be displayed on the prescription list screen P25, receives the prescription information, and receives the prescription list screen P25.
  • a configuration is also conceivable in which the prescription information can be slide-displayed in response to a flick operation in the vertical direction.
  • the control unit 11 When the display position corresponding to any of the prescription information is operated on the prescription list screen P25, the control unit 11 changes the display color of the display position corresponding to the prescription information and is in the selected state. Indicate. Thereafter, when the user performs a right or left flick operation on the touch panel 13 with any of the prescription information selected, the control unit 11 displays details of the prescription information being selected.
  • the indicated prescription drug information screen P27 is displayed on the touch panel 13.
  • FIG. 27 is a diagram showing an example of the prescription drug information screen P27. On the prescription drug information screen P27, information on prescription drugs (drug name, usage, number of days, prescription amount, etc.) is displayed for each recipe included in the prescription information.
  • the control unit 11 changes the display color of the display position corresponding to the recipe and is in a selected state. Indicates. Thereafter, when the determination key displayed after the user performs a touch operation or an upward flick operation on the development area A271 of the prescription drug information screen P27 is operated, the control unit 11 performs the selection. And the recipe screen P23 is displayed. In addition, in the prescription medicine information screen P27, the control unit 11 changes the display position of the prescription medicine or recipe that has already been weighed to a display color different from the display color indicating that it is being selected. Indicate.
  • step S552 the control unit 11 causes the touch panel 13 to display a recipe list screen P28 including a list of recipe information obtained by disassembling the prescription information for each recipe.
  • the recipe list screen P28 displays a list of recipe information that has not been weighed by the chemical weighing device 10 when the type of system linkage is “unprocessed”.
  • a list of recipe information for which weighing has been completed by the chemical weighing device 10 is displayed on the recipe list screen P28.
  • FIG. 28 and FIG. 29 are diagrams showing an example of the recipe list screen P28. As shown in FIG. 28, items such as patient ID, patient name, medical department, medicine name, and deletion corresponding to the recipe information are displayed on the recipe list screen P28.
  • a development area A281 is displayed on the recipe list screen P28.
  • the control unit 11 expands the display area of the development area A281 as shown in FIG.
  • various touch keys indicating the contents that can be operated on the recipe list screen P28 are displayed.
  • the said control part 11 is a predetermined number of presets which can be simultaneously displayed on the said recipe list screen P28 similarly to the case where the said prescription list screen P25 is displayed.
  • the host system 70 is requested to transmit the recipe information.
  • the control unit 11 receives the predetermined number of recipe information from the host system 70 and stores the received recipe information in the data storage unit 15. Also in this case, the control unit 11 switches the content of the recipe information displayed on the recipe list screen P28 in accordance with the operation of “previous data” or “next data” displayed in the development area A251.
  • the host system 70 Can execute exclusive processing of the recipe information or the prescription information.
  • the control unit 11 controls the user's upper and lower of the recipe list screen P28.
  • the recipe information displayed on the recipe list screen P28 can be slid and changed in accordance with a direction flick operation.
  • the said control part 11 will change the display color of the display position corresponding to the said recipe information, and is a selection state. Indicate. Thereafter, when the user performs a right or left flick operation on the touch panel 13 with any of the recipe information selected, the control unit 11 displays details of the selected recipe information.
  • the indicated prescription drug information screen P30 is displayed on the touch panel 13.
  • FIG. 30 shows an example of the prescription drug information screen P30. On the prescription drug information screen P30, information on prescription drugs (medicine name, usage, number of days, prescription amount, etc.) included in the recipe information is displayed.
  • control unit 11 is displayed after the user performs a touch operation or an upward flick operation on the development area A281 of the recipe list screen P28 or the development area A301 of the prescription drug information screen P30.
  • the enter key is operated, the currently selected recipe information is determined as a weighing target, and the prescription screen P23 is displayed.
  • the control unit 11 indicates this by changing the display position of the prescription drug that has already been weighed to a different display color.
  • step S56 the control unit 11 determines whether the system interlocking type of the medicine weighing device 10 is set to “patient ID” or “exchange ticket number”.
  • Patient ID is an operation mode in which the control unit 11 reads the prescription information corresponding to a patient ID input by a user operation on the touch panel 13 from the data storage unit 15 or the host system 70.
  • exchange ticket number is an operation mode in which the control unit 11 reads the prescription information corresponding to the exchange ticket number input by a user operation on the touch panel 13 from the data storage unit 15 or the host system 70. .
  • control unit 11 shifts the process to step S57, and sets “patient ID” and “patient ID”. If it is not a “voucher ticket number” (No in S57), the process returns to step S51.
  • step S57 the control unit 11 inputs a patient ID when the type of system linkage is “patient ID”, and an exchange ticket number when the type of system linkage is “exchange ticket number”.
  • An input screen P31 is displayed on the touch panel 13.
  • FIG. 31 is a diagram showing an example of the input screen P31 for inputting the patient ID.
  • the control unit 11 extracts prescription information corresponding to the patient ID from the prescription information stored in the data storage unit 15. And the said control part 11 displays the prescription information corresponding to the said patient ID on the said prescription list screen P25.
  • the type of the system linkage is “exchange ticket number”
  • an input unit for inputting the exchange ticket number is displayed on the input screen P31, and the exchange ticket number input to the input unit is displayed. The corresponding prescription information is read out.
  • the generic drug use process described here may be executed by the drug weighing device 10 in a configuration in which the drug weighing device 10 is not connected to the host system 70, for example, in the drug weighing system 1.
  • the prescription information displayed on the prescription screen P23 includes a prescription drug of “Gaster powder 10%”. The case where “%” is read as the name of the contained medicine will be described as an example.
  • step S61 the control unit 11 executes a process for selecting a change target to be changed to the stored medicine name read in step S3 from the prescription drug names included in the prescription information. Specifically, the control unit 11 displays a selection screen for selecting a change target from the prescription drug name included in the prescription information, and displays the prescription drug name selected by a user operation on the touch panel 13. Select as change target. In addition, when the said prescription medicine name is one, the said control part 11 may select the one prescription medicine name as change object automatically.
  • step S62 the control unit 11 determines whether or not the prescription information includes non-changeable information indicating that the prescription drug name selected in step S61 is incapable of being changed to a generic drug. Judging. And the said control part 11 makes a process transfer to step S63, when the said change impossible information is contained in the said prescription information (Yes side of S62). On the other hand, when the change impossible information is not included (No in S62), the control unit 11 shifts the process to step S611 and executes a prescription medicine changing process (see FIG. 34) described later. The non-changeable information is added to the prescription information in the host system 70. In addition, the control unit 11 may be added in accordance with a user operation on the touch panel 13.
  • step S63 the control unit 11 displays on the touch panel 13 that the change of the prescription drug to a generic drug is prohibited, notifies the user, and shifts the process to step S64. That is, the prescription medicine is not changed to the generic medicine corresponding to the name of the contained medicine.
  • step S64 the control unit 11 determines whether or not another prescription drug name that has not been selected in step S61 is included in the prescription information. Here, if the said control part 11 judges that the other prescription medicine which is not selected is contained (Yes side of S64), it will transfer a process to the said step S61, and the other said prescription medicine which is not selected will be. If it is determined that it is not included (No in S64), the generic drug use process is terminated.
  • step S71 the control unit 11 determines whether or not the stored medicine name read from the medicine bottle by the barcode reader 17 is registered as a generic medicine of the prescription medicine in the generic medicine master.
  • the said control part 11 judges that the said accommodated medicine name is registered as the said generic drug (Yes side of S71)
  • it will transfer a process to step S72.
  • the control unit 11 shifts the process to step S711 to register the generic drug described later (see FIG. 37). Execute.
  • step S72 the control unit 11 changes the prescription drug selected in step S61 to the generic drug read as the stored medicine name, redisplays the prescription screen P23, and changes the prescription drug. End the process.
  • FIG. 35 is a diagram showing an example of the prescription screen P23 after the prescription drug is changed to the generic drug. As shown in FIG. 35, in the prescription screen P23 displayed in the step S72, “Gaster powder 10%” included as a prescription drug in the prescription information is the name of the generic drug “Gasdog powder 10%”. It has been changed to.
  • the control unit 11 provides the change history information (for example, the change date and time, the name of the pharmacist responsible for the change, and the content of the change). It may be recorded as the weighing result. Thereby, the history which changed the prescription medicine into the generic medicine etc. can be checked easily later.
  • the change history information for example, the change date and time, the name of the pharmacist responsible for the change, and the content of the change. It may be recorded as the weighing result. Thereby, the history which changed the prescription medicine into the generic medicine etc. can be checked easily later.
  • the control unit 11 may cause the touch panel 13 to display the drug list screen P33 of the original drug and the generic drug corresponding to the stored drug name based on the generic drug master.
  • FIG. 36 shows an example of the medicine list screen P33.
  • the medicine list screen P33 As shown in FIG. 36, on the medicine list screen P33, the general name (famotidine) of the medicine corresponding to the contained medicine name, the original medicine and the generic medicine corresponding to the contained medicine name are displayed.
  • the medicine list screen P33 when the user performs a touch operation for selecting either the original medicine or the generic medicine being displayed, the display color of the display position of the selected medicine name is changed. The selection status is indicated.
  • the stored medicine name read by the barcode reader 17 is selected.
  • the control unit 11 changes the prescription drug to the generic drug selected on the drug list screen P33.
  • the cancel key K332 on the medicine list screen P33 is operated, the control unit 11 cancels the registration of the generic drug and ends the change process for the prescription medicine.
  • step S81 the control unit 11 displays on the touch panel 13 that the stored medicine name is not registered as the generic drug, and whether or not to register the contained drug name as the generic drug.
  • a confirmation message (see, for example, FIG. 9C) is displayed.
  • step S82 when the control unit 11 determines that an operation for registering the stored medicine name as the generic drug has been performed on the touch panel 13 (Yes in S82), the process proceeds to step S83. Transition. In addition, the said control part 11 will complete
  • step S83 the control unit 11 causes the touch panel 13 to display a maintenance screen P38 for registering the generic drug in the generic drug master. Specifically, when the prescription drug name selected in step S61 corresponds to the name of the original drug registered in the drug master, the control unit 11 associates the name of the original drug with the name of the subsequent drug. The maintenance screen P38 for registering a pharmaceutical product is displayed. On the other hand, if the prescription drug name selected in step S61 corresponds to the generic drug name registered in the generic drug master, the generic drug name corresponding to the generic drug name is set to the generic drug master. Identify based on. Then, the maintenance screen P38 for registering the generic drug name in association with the specified generic drug name is displayed.
  • FIG. 38 shows an example of the maintenance screen P38.
  • the maintenance screen P38 displays the name of the original drug and the registered generic drug corresponding to the branded pharmaceutical, and the stored drug name is added as the generic drug of the branded pharmaceutical.
  • the displayed status is displayed.
  • the maintenance screen P38 shown in FIG. 38 when “Gasdogsan 10%” is not registered as a generic drug of “Gastersan 10%” which is the original drug, the “Gasdogsan” is stored as the stored medicine name.
  • a display example in the case where “10%” is read is shown.
  • Steps S84 to S85 the control unit 11 waits for an operation of the registration key K381 or the end key K382 on the maintenance screen P38 (No side of S84 and S85).
  • the control unit 11 judges that the said registration key K381 was operated (Yes side of S84)
  • it will transfer a process to step S86.
  • the control unit 11 determines that the end key K382 is operated (Yes in S85)
  • the control unit 11 ends the registration process of the generic drug without registering the contained drug as the generic drug.
  • step S86 the control unit 11 registers the prescription drug as the generic drug in the generic drug master and confirms whether or not to change to the generic drug registered on the maintenance screen P38. Display.
  • step S87 the control unit 11 causes the touch panel 13 to display the prescription screen P23 (see FIG. 35) after changing the prescription drug to the generic drug as in step S72.
  • step S87 the control unit 11 ends the registration process of the generic drug without changing the prescription drug to the generic drug.
  • Step S91 When the drug weighing apparatus 10 is turned on and the drug weighing apparatus 10 is activated, the control is performed by the CPU 111 executing the kernel 114 and the OS 115 stored in the SD card 112 in step S91.
  • the medicine weighing device 10 can be controlled by the unit 11.
  • step 92 the control unit 11 confirms whether or not the data storage unit 15 is connected to the USB port 16.
  • step S93 Yes side of S93
  • step S931 the control unit 11 shifts the process to step S931, and the connection of the data storage unit 15 is confirmed. If not (No in S93), the process proceeds to step S94.
  • step S94 the control unit 11 activates the single weighing application 116 in the SD card 112 to operate the chemical weighing apparatus 10 as an electronic balance. Thereafter, when a power OFF operation is performed on the touch panel 13 in step S95 (Yes side of S95), the control unit 11 executes a shutdown process of the chemical weighing device 10 in the subsequent step S96 to turn on the power. Turn off.
  • Steps S931 to S932> On the other hand, when the connection of the data storage unit 15 is confirmed, the control unit 11 executes a preset update process in the subsequent step S931, and then activates the drug weighing program 154 (S932). Is transferred to step S95.
  • the control unit 11 determines whether or not the medicine weighing program 154 stored in the data storage unit 15 is the latest.
  • the determination as to whether or not the medicine weighing program is up-to-date is made, for example, by acquiring update information from the Internet or the like via the host system 70 or the network N.
  • the control unit 11 downloads the latest medicine weighing program 154 and updates the medicine weighing program 154 in the data storage unit 15.
  • the control unit 11 stores data such as the prescription information, the weighing result, the filling record, the medicine usage amount, the incident history, and the error history, which have passed a preset deletion target period, in the data storage unit 15. Delete from database 155.
  • the filling record is recorded as a history of weighing with the medicine weighing device 10 and filled in a medicine bottle.
  • the filling amount for each medicine bottle is recorded, and the amount of medicine used is the history of the medicine weighed with the medicine weighing device 10. It is the usage amount for each medicine recorded.
  • the incident history is information on an incident that has occurred in the medicine weighing apparatus 10 or an incident that has been input to the medicine weighing apparatus 10 from the outside
  • the error history is information on an error that has occurred in the medicine weighing apparatus 10.
  • control unit 11 backs up various data such as the prescription information, the weighing result, various master information (generic drug master, etc.), and system setting information stored in the database 155 of the data storage unit 15. .
  • the control unit 11 manages the database 155 using a well-known database management system such as SQL Lite (registered trademark), MySQL (registered trademark), or PostgreSQL (registered trademark) using the SQL language. . Therefore, the control unit 11 uses the backup function of the database management system to store each table data such as the prescription information, the weighing result, various master information, and system setting information stored in the database format.
  • the data is output as a dump file 156 and stored in the data storage unit 15.
  • the control unit 11 leaves only the latest database dump file 156 or only the preset number of the database dump files 156, and the previous database dump file 156 is deleted.
  • the backup destination by the control unit 11 is not limited to the data storage unit 15, but may be the medicine packaging device 20, the host system 70, or a server device on the Internet.
  • the chemical weighing device 10 is backed up at the time of start-up, even if an abnormality occurs in the chemical weighing device 10 and then the database is damaged, at least the chemical weighing is performed. The database can be restored until the device 10 is activated.
  • the drug weighing process similar to the drug weighing process is executed by the control unit 11.
  • the method for reading the prescription information in the step S1 executed by the medicine weighing apparatus 10 is different.
  • the control unit 11 can accept the prescription information from the host system 70 in addition to reading the prescription information using the barcode reader 17. That is, in the step S1 of the drug weighing process, the control unit 11 receives any of the prescription information received from the host system 70 and stored in the data storage unit 15 in response to a user operation on the touch panel 13.
  • step S2 If the prescription information has been selected, it is determined that the prescription information has been input, and the process proceeds to step S2.
  • the control unit 11 acquires the prescription information acquired from the host system 70 and stored in the data storage unit 15 in chronological order. Also when the automatic reading is performed, the process proceeds to step S2.
  • the control unit 11 executes an automatic numbering process for setting a tray number corresponding to the recipe.
  • the tray number is a 4-digit value that is automatically set by the control unit 11 in the drug weighing device 10 and is set in advance so as not to be duplicated for each drug weighing device 10 in the drug weighing system 2. Is set within the specified range. For example, as shown in FIG. 17, when four drug weighing devices 10 are connected to the drug weighing system 2, “0000” to “1000”, “1001” to “1001” Tray numbers from “2000”, “2001” to “3000”, “3001” to “4000” are assigned in advance.
  • the tray number is a number assigned to each recipe, and is numbered as a common number for each of the prescription drugs even when a plurality of prescription drugs are included in the recipe.
  • the control unit 11 confirms that the tray number does not match the tray number stored in the shared folder provided in the data storage unit 26 of each medicine packaging device 20. Specifically, only the tray number for which the packaging process in the medicine packaging apparatus 20 has not been completed remains in the shared folder, and the tray number for which the packaging process has been completed is stored in the medicine packaging apparatus 20. Is erased by the control unit 21.
  • the control unit 11 of the medicine weighing device 10 stores the tray number in the shared folder of the medicine packaging device 20 when the tray number is not stored in the shared folder. The control unit 11 adds correspondence information with the tray number to the recipe information corresponding to the tray number set here in the prescription information stored in the data storage unit 25.
  • the timing at which the control unit 11 records the correspondence between the recipe information and the tray number in the data storage unit 25 is the timing at which the RFID tag 31 records the tray number by the RFID reader / writer 14. May be.
  • the timing at which the control unit 11 stores the recipe information in the data storage unit 25 may be after the tray number is associated with the recipe information.
  • the control unit 11 sets the number next to the tray number as the tray number corresponding to the recipe. To do. That is, the control unit 11 assigns a tray number that is not stored in the shared folder to the recipe. Thereby, in the said chemical
  • the shared folder may be provided in each medicine packaging device 20.
  • the shared folder is provided only in any one of the medicine packaging apparatuses 20, and the other medicine packaging apparatus 20 refers to or erases the tray number of the shared folder.
  • FIG. 40 is a diagram showing an example of the No. machine selection screen P40.
  • a machine number selection key K401 for selecting a machine number preset for each medicine packaging apparatus 20 is displayed on the machine number selection screen P40.
  • the control unit 11 displays the number of machine numbers set in advance by a pull-down menu in accordance with the operation of the machine number selection key K401, and inputs the machine number selected from the pull-down menu to the machine number selection key K401.
  • the number of machine numbers displayed in the pull-down menu is considered to be the number of the medicine packaging devices 20 connected to the medicine weighing system 2 or the maximum number connectable to the medicine weighing system 2. .
  • a hopper selection key K402 for selecting a hopper to be used in the packaging process in the medicine packaging apparatus 20 is displayed.
  • the control unit 11 displays a hopper number preset by a pull-down menu in accordance with an operation of the hopper selection key K402, and inputs the hopper number selected by the pull-down menu to the hopper selection key K402. For example, in the pull-down menu, “A” indicating the hopper 25A provided in the medicine packaging device 20, “B” indicating the hopper 25B, or “AB” indicating that any of the hoppers 25A and 25B may be used. "May be displayed.
  • the control unit 11 changes the pull-down menu display in the hopper selection key K402 according to the number of hoppers provided in the medicine packaging device 20 corresponding to the machine number selected by the machine selection key K401. It is also possible to do.
  • the unit selection key K401 and the hopper selection key K402 are displayed, and the case where the unit number and the hopper number are input at the same time is given as an example, but the present invention is not limited thereto.
  • the control unit 11 displays a machine number selection screen on which only the machine number selection key K401 is displayed in the step S2 and inputs the machine number, and then the prescription drug weighing in the drug weighing device 10 is performed. It is conceivable that when the work is completed, a hopper selection screen on which only the hopper selection key K402 is displayed is displayed to input the hopper number. Thereby, when a plurality of prescription medicines are contained in one recipe, it is possible to select the hopper for each prescription medicine. Also, the trouble of inputting the machine number for each prescription drug is omitted.
  • the control unit 11 uses the RFID reader / writer 14 to input the tray number, the machine number, and the hopper number to the RFID tag 31. Write to.
  • the control unit 21 uses the RFID reader / writer 14 to input the tray number, the machine number, and the hopper number to the RFID tag 31. Write to.
  • the recipe information stored in the data storage unit 26 in association with the tray number is read from the data storage unit 26 by the control unit 21.
  • the machine number and the hopper number are stored in the shared folder of the data storage unit 26 in association with the tray number, and the control unit 21 selects the machine number from the shared folder according to the tray number. It is also conceivable to read out the hopper number.
  • the control unit 11 can also write information on the tray number, the machine number, and the hopper number in the RFID tag 31 not in the prescription drug unit but in the recipe unit. .
  • the control unit 11 shifts the “registration” key on the prescription screen P23 (see FIG. 23) to an operable state. , “Please set the medicine tray” is displayed on the touch panel 13.
  • the control unit 11 uses the RFID reader / writer 14 to input the tray number, the machine number, and the hopper number corresponding to the recipe. Write to 31.
  • the control unit 21 reads the tray number from the RFID tag 31 of the medicine sheet 30, and the recipe information corresponding to the tray number and the weighing result are data to be packaged. As shown in FIG.
  • the recipe information includes a prescription date, a tray number, a prescription number, a data unit, a drug detail number, a drug code, a patient ID, a voucher number, a machine number, hopper information, a state classification, and the like.
  • the chemical specification number is information for specifying the weighing result corresponding to the recipe information.
  • the hopper information is information indicating a hopper to be used in the medicine packaging device 20, for example, “A” when the hopper 25A is selected, “B” when the hopper 25B is selected, When it is selected that either the hopper 25A or the hopper 25B is selected, it is represented by “AB”.
  • the control unit 21 reads the recipe information corresponding to the tray number from the data storage unit 26 based on the tray number read from the RFID tag 31 by the RFID reader / writer 24. And the said control part 21 displays the said recipe information on the packaging input screen P41 displayed on the said touch panel 23.
  • FIG. 41 and 42 are diagrams showing an example of the packaging input screen P41.
  • the packaging input screen P41 includes a display area A411 in which information such as the number of prescription drugs included in the recipe information is displayed.
  • the packaging input screen P41 includes a list of prescription medicines already read from the RFID tag 31 by the RFID reader / writer 24 among prescription medicines included in the recipe information, the weighing result of each prescription medicine, A display area A412 on which a packaging pattern, the hopper number, and the like are displayed is included. Thereby, the user can easily grasp the number of medicines that are currently insufficient for starting the packaging operation of the recipe in the medicine packaging device 20.
  • the prescription and the list of prescription medicines displayed on the packaging input screen P41 it is also possible to grasp the names of medicines that are currently insufficient to start the packaging operation of the recipe information. is there.
  • control unit 21 reads the tray number from the RFID tag 31 by the RFID reader / writer 24, a list of prescription medicines included in the recipe information corresponding to the tray number is input to the package. It can also be displayed on the screen P41.
  • said control part 21 is a character ("(circle)" which shows whether the information of each of the said prescription medicine was read from the said RFID tag 31 in the said medicine name list displayed on the said packaging input screen P41. It is conceivable to display confirmation information such as “x” or an image. Thereby, the user can grasp
  • the presence / absence of reading of each prescription medicine on the packaging input screen P41 may be represented by changing the display color (presence / absence of grayout) of each prescription medicine, for example.
  • a plurality of the prescription chemicals included in the recipe information is placed on one dispensing sheet 30, and the hopper 25A or the hopper 25B is charged in units of the recipe.
  • the control unit 21 starts a packaging operation related to the recipe information without displaying the packaging input screen P41. Display the monitor screen for
  • the control unit 21 executes a medicine printing process for printing out the weighing result output from the medicine weighing device 10 on the wrapping paper using the printing unit 27. It is possible to do.
  • the control unit 21 prints preset medicine information at the beginning or end of a series of packaging papers output by the packaging operation of the medicine packaging device 20. Add the wrapping paper and output. Note that the content of the drug inspection information can be changed by the control unit 21 in response to a user operation on the touch panel 23 in an initial setting or the like in the drug packaging device 20.
  • FIGS. 43 and 44 are diagrams showing an example of a printed image of the drug information.
  • the drug information shown in FIG. 43 includes the date (November 26, 2007), patient name (Taro Yuyama), exchange ticket number (5678), number of days (3), and total weight (369.0000 g) of drug packaging. included.
  • the total weight of the medicine packaging is a total value of the total weight of the wrapping paper used for the packaging of the recipe unit and the total weight of the prescription medicine included in the recipe information.
  • the control unit 21 adds the total weight of the wrapping paper included in the recipe information output from the chemical weighing device 10 and the weighing result output from the chemical weighing device 10. It is possible to calculate the total weight of the medicine package.
  • the control unit 11 multiplies the number of wrapping papers used for the wrapping of the recipe unit by a preset weight per sheet.
  • the total weight of the wrapping paper is calculated and recorded as one item of the recipe information.
  • the control unit 11 determines the weight per one piece of the wrapping paper, for example, of the wrapping paper selected by operating the previous setting key K235 (see FIG. 24) for setting the type of the wrapping paper. It is possible to judge according to the combination of the material and the length.
  • the medicine information is printed on the packaging paper, for example, the user can audit the packaging operation for each recipe without referring to a prescription.
  • the user separates the wrapping paper on which the drug inspection information is printed from a series of wrapping papers, and weighs the total weight of the remaining wrapping paper with the medicine weighing device 10 or another electronic balance. . Then, the user performs an audit by comparing the total weight of the medicine package printed as the medicine information with the actual weighing value.
  • the drug information shown in FIG. 44 includes a drug name, a packaging pattern (11111111), an expiration date (November 26, 2007), a lot number, an actual measurement value (369.0000 g), and a theoretical value (369.0000 g). ) And other information.
  • the packaging pattern is information for indicating the dosing time (morning, noon, evening, etc.) determined by the recipe information at positions of “1” and “0” in a plurality of preset digits.
  • the actual measurement value is the total weight of the prescription drug actually weighed in the drug weighing device 10 and is information included in the weighing result output from the drug weighing device 10.
  • the theoretical value is the theoretical total weight of the prescription drug calculated based on the daily amount, usage, number of days, etc.
  • the control unit 21 subtracts the weight of the prescription drug that is not to be taken within the time of taking from the maximum weight obtained by multiplying the number of days by the value obtained by multiplying the daily dose and the number of times taken by the usage.
  • the theoretical value is calculated. Specifically, if the usage is set to morning, noon, and evening, and both the start time and end time are noon, the weight of the medicine for the morning of the first day and the last day The theoretical value is calculated by excluding the total of the evening weight of the medicine and the weight of the medicine from the maximum weight. Even in such a case, the user can audit the packaging of each recipe using the medicine weighing device 10 or another electronic balance while referring to the packaging paper on which the drug information is printed. it can.
  • the medicine weighing device includes weighing means, prescription information reading means, stored medicine information reading means, and control means.
  • the weighing means weighs the drug.
  • the prescription information reading unit reads prescription information including prescription drug identification information for identifying one or a plurality of prescription drugs recorded in the prescription from the prescription.
  • the stored medicine information reading means reads stored medicine information including stored medicine identification information for identifying the stored medicine recorded in the medicine container from the medicine container.
  • the control means selects the prescription drug as a weighing target, A weighing screen for weighing the prescription drug is displayed on the display means.
  • the prescription information includes, for example, prescription delivery date, patient ID, patient name, patient birth date, dosage form information (internal use, external use, etc.), drug information (drug code, drug name, dose), usage information (1 Etc.) after 3 meals a day).
  • the prescription medicine identification information and the contained medicine identification information are information such as a medicine name or a medicine code that can specify the kind of medicine.
  • the prescription medicine when the contained medicine corresponds to any of the prescription medicines, the prescription medicine is automatically selected as a weighing target and displayed on the weighing screen. That is, according to the present invention, the user only has to make the stored medicine information reading means read the stored medicine information of the drug container, and in the medicine weighing device, the collation of the prescription medicine and the stored medicine, The selection of the prescription medicine to be weighed in the prescription information can be realized at the same time. Thereby, when a plurality of prescription medicines are included in the prescription information, an operation for selecting a prescription medicine to be weighed can be omitted, and the dispensing efficiency by a user such as a doctor or a pharmacist is improved. Can do. Therefore, according to the present invention, it is possible to easily perform accurate weighing of medicines in accordance with a prescription without cooperation with a host system such as a dispensing support system.
  • the medicine weighing device includes a code reading means for reading information from a bar code or a two-dimensional code.
  • the prescription information reading means reads the prescription information by the code reading means from the barcode or two-dimensional code recorded in the prescription
  • the contained medicine information reading means is a bar recorded in the medicine container. It is conceivable to read the stored medicine information from the code or the two-dimensional code by the code reading means.
  • the user can accurately and easily follow the prescription by causing the code reading unit to sequentially read a two-dimensional code of a prescription and a barcode of a medicine container (such as a medicine bottle). The drug can be weighed.
  • the user can check the stored medicine and the prescription medicine and select the medicine to be weighed in the medicine weighing apparatus only by the operation of causing the code reading means to read the barcode recorded in the medicine container. Can be realized.
  • the prescription information reading unit and the stored medicine information reading unit can each serve as the code reading unit, a new configuration is provided in the conventional configuration including the stored medicine information reading unit and the code reading unit. There is no need to add elements.
  • the bar code is a one-dimensional code having information only in the horizontal direction, such as a JAN code or RSS.
  • the two-dimensional code has information in the horizontal direction and the vertical direction, and is, for example, a QR code (registered trademark).
  • the prescription information reading unit and the contained medicine information reading unit may read information directly from the prescription or the medicine container using, for example, a character recognition technique or an image recognition technique.
  • the chemical weighing device further includes a code reading unit that reads information from a bar code or a two-dimensional code and a wireless reading unit that reads information from an information recording medium by wireless communication
  • the prescription reading means reads the prescription information by the code reading means from a bar code or a two-dimensional code recorded in the prescription
  • the stored medicine information reading means is an information recording provided in the medicine container. It is conceivable to read the stored medicine information from a medium by the wireless reading means.
  • the prescription information includes information on the prescription amount of the prescription medicine recorded in the prescription.
  • the weighing screen includes, for example, display of the prescription medicine to be weighed and the prescription amount of the prescription medicine.
  • control means displays the fact when the contained medicine does not correspond to any of the prescription medicines. As a result, the user can be warned that the selection of the chemical container is incorrect.
  • the display means performs the display using characters, images, sounds, light, or the like.
  • the medicine weighing device has a first input means for inputting completion of weighing for each prescription drug, a second input means for inputting completion of weighing for each prescription information, and the second input. If there is a prescription drug that has not been completed for weighing by the first input means in the prescription drug included in the prescription information for which the completion of weighing has been input by the means, the fact is not displayed. And a completion display means. Thereby, it is possible to prevent forgetting the weighing related to the prescription medicine included in the prescription information.
  • the medicine weighing device stores generic drug information in which generic drug information in which a correspondence relationship between generic drug identification information for identifying the generic drug and generic drug identification information for identifying the generic drug (generic drug) is defined is stored.
  • the original drug identification information and the generic drug identification information are information such as a drug name or drug code that can specify the type of drug.
  • the control means uses the generic drug when the contained drug corresponds to any of the generic drugs and the generic drug corresponding to the generic drug corresponds to any of the prescription drugs.
  • a confirmation screen for arbitrarily selecting whether or not to perform is displayed, and when the operation input for using the generic drug is performed according to the confirmation screen, the stored medicine is selected as a weighing target. It is done.
  • the generic drug refers to a drug before the expiration of the patent right, and the generic drug refers to a drug supplied from another company after the expiration of the validity period.
  • control means displays a registration screen for registering the stored medicine as the generic drug in the generic drug information when the contained drug does not correspond to either the prescription drug or the generic drug. It is desirable to edit the generic drug information in response to an operation input according to the registration screen. Accordingly, the user can easily edit the generic drug information and enrich the contents during daily operations using the drug weighing device.
  • the medicine weighing device is a recording means for recording at least weighing drug information relating to the medicine weighed by the weighing means on a recording medium provided on a medicine placing member on which the medicine is placed when weighing by the weighing means. It is conceivable to have Furthermore, the recording means may further record a part or all of the prescription information on the recording medium.
  • the recording medium is, for example, an RFID tag.
  • the weighing medicine information and the prescription information are read from the recording medium, and the weighing medicine information And / or predetermined appropriate processing can be performed based on the prescription information.
  • the medicine weighing device includes medicine information storage means storing medicine information including appropriate amount information relating to a predetermined appropriate amount corresponding to each medicine, and a weighing value measured by the weighing means is determined for each medicine. It is conceivable to further include an auditing unit that audits whether or not it is within the range of the appropriate amount set in advance based on the appropriate amount information stored in the medicine information storage unit.
  • the medicine information includes pre-determined simultaneous medication prohibition information related to a medicine that is prescribed for each medicine and prohibited to be taken at the same time
  • the auditing means is included in the prescription information. It is conceivable to audit whether or not a plurality of medicines are prohibited from being taken at the same time based on the simultaneous medicine prohibition information stored in the medicine information storage means.
  • the medicine weighing apparatus alone can be audited with respect to the prohibition of the normal dose and the simultaneous use without using another information processing apparatus such as a computer. Accordingly, it is possible to prevent the prescription of a medicine exceeding the normal dose or the prescription of a plurality of medicines causing a change in composition or a side effect when taken at the same time at the medicine weighing stage in the medicine weighing device.
  • the medicine packaging apparatus selects an information reading unit for reading information from the recording medium, and an input destination for selecting and displaying one of the input units based on the weighed drug information read by the information reading unit. Display means. Thereby, in the medicine packaging device, which one of the feeding parts is used is displayed based on the weighed medicine information, so that it is possible to prevent a human error of a user who mistakes the feeding part for feeding medicine. .
  • the packaging unit includes a dividing unit that divides the powder that has been introduced into each of the input units into one dose unit, and a packaging unit that packages the powder that has been divided by the dividing unit. It is conceivable to include a packaging control means for causing the dividing means or the packaging means to execute an operation preset for each type of the powder according to the type of medicine included in the weighed medicine information. This makes it possible to perform a predetermined appropriate process for each type of powder based on information on the type of powder contained in the weighing medicine information and the prescription information, for the packaging operation in the packaging unit. .
  • the present invention may be regarded as an invention of a medicine weighing program for causing a computer to execute a prescription information reading process, a stored medicine information reading process, and a control process.
  • the prescription information reading step reads prescription information including prescription drug identification information for identifying one or a plurality of prescription drugs recorded in the prescription from the prescription.
  • stored medicine information reading step stored medicine information including stored medicine identification information for identifying the stored medicine recorded in the medicine container is read from the medicine container.
  • the control step corresponds to any one of the prescription drugs indicated by the prescription drug identification information read by the prescription information reading step, the stored medicine indicated by the stored medicine identification information read by the stored medicine information reading step.
  • the prescription drug is selected as a weighing target, and a weighing screen for the prescription drug as a weighing target is displayed on the display means.
  • the present invention may be understood as an invention of a computer-readable recording medium that records the medicine weighing program.
  • Chemical weighing system 2 Chemical weighing system 10: Chemical weighing device 11: Control unit 111: CPU 112: SD card 114: Kernel 115: OS 116: Scale unit application 113: RAM 12: Balance unit 13: Touch panel 14: RFID reader / writer 15: Data storage unit 151: Log 152: Setting file 153: Form layout file 154: Drug weighing program 155: Database 156: Database dump file 16: USB port 17: Bar code Reader 18: Printer 19: Balance stand 20: Medicine packaging device 21: Control unit 22: Packaging unit 23: Touch panel 24: RFID reader / writer 25: Supply hopper 25A, 25B: Hopper 26: Data storage unit 27: Printing unit 30: Drug Sheet 31: RFID tag 70: Host system 71: Control unit 72: Data storage unit

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JPWO2015141660A1 (ja) * 2014-03-18 2017-04-13 株式会社湯山製作所 薬剤払出し装置
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JP2020175257A (ja) * 2014-05-02 2020-10-29 株式会社湯山製作所 鑑査支援システム、鑑査支援装置、鑑査支援プログラム
JP7004040B2 (ja) 2014-05-02 2022-01-21 株式会社湯山製作所 鑑査支援システム、鑑査支援装置、鑑査支援プログラム
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JP2022069573A (ja) * 2015-04-20 2022-05-11 株式会社湯山製作所 薬品払出装置
JP7277687B2 (ja) 2015-04-20 2023-05-19 株式会社湯山製作所 薬品払出装置
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JP2020124441A (ja) * 2019-02-06 2020-08-20 株式会社トーショー 散薬秤量システム
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WO2020162413A1 (ja) * 2019-02-06 2020-08-13 株式会社トーショー 散薬秤量システム

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