JP7225308B2 - Drug information output device and program - Google Patents

Description

The present invention relates to a medicine information output device and program .

Conventionally, when a patient brings a prescription issued by a hospital, clinic, etc. to a pharmacy, the pharmacy delivers the drug described in the prescription to the patient, as well as a drug information document that describes the drug to be delivered. Sometimes.
In order for the pharmacy to create such a drug information document, along with the recent development of information processing technology, information processing technology has been introduced, and a computer equipped with a database that stores drug descriptions and photos Increasingly, when a person enters prescription information into a computer, the computer generates a drug information sheet for the prescription drug. Such a drug information document is useful for a patient to grasp drug information including how to take the drug.
For example, Patent Literature 1 discloses a creation system for printing a medicine instruction book containing names and photographs of issued medicines, as well as a calendar indicating when and how much medicine is to be used.

JP-A-2001-47773

However, even if there was a change in the content of the drug delivered in the past and the content of the drug delivered this time, it was difficult to grasp the change. .

SUMMARY OF THE INVENTION Accordingly, an object of the present invention is to make it possible to easily grasp changes in the contents of delivery of medicines.

In order to achieve the above object, a medicine bag according to one aspect of the present invention is a medicine bag for containing a medicine, which is formed into a bag shape by bonding a predetermined portion of a rectangular sheet of paper. In the area, a display area for displaying drug information including a drug change indication indicating that the drug has been changed or a dosage and administration change indication indicating that the dosage and administration has been changed is provided. It is characterized in that an adhesive applying portion indicating an area to which the adhesive is applied is provided on the peripheral portion.

In order to achieve the above object, a drug information output device of one aspect of the present invention includes prescription storage means for storing information on a patient's prescription; drug information output means for outputting drug information data including a drug change display indicating that the drug has been changed or a dosage and administration change display indicating that the dosage and administration has been changed, based on the change in the

To achieve the above object, a program according to one aspect of the present invention includes steps of storing information on a patient's prescription; and causing a computer to generate drug information data including a drug change indication indicating that the drug has been changed or a dosage and administration change indication indicating that the dosage and administration has been changed.

Advantageous Effects of Invention According to the present invention, it becomes possible to easily grasp changes in the contents of delivery of medicines.

It is a figure which shows the outline|summary of medicine provision business. It is a figure which shows the functional structure of a medication information output device. It is a figure which shows the prescription database of a memory|storage part. It is a figure which shows the drug database of a memory|storage part. It is a flowchart which shows the flow of a process of a medication information output device. It is a figure which shows an example of the drug information which a drug information output device outputs. It is a figure which shows an example of the drug information conventionally output. It is a figure which shows an example of the drug information which a drug information output device outputs. It is a figure which shows an example of the drug information which a drug information output device outputs.

BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, embodiments of the present invention will be described with reference to the drawings.

The application scene of the drug information document output by the drug information output device 10 of the present invention will be described with reference to FIG.
FIG. 1 is a conceptual diagram showing medicine provision work in a pharmacy. FIG. 1(1) shows the flow of each work, and FIG. 1(2) shows the contents of each work.
With reference to FIG. 1 (1), the drug provision service dispenses the drug according to the prescription after receiving the prescription from the patient at the window, and if the dispensing is deemed appropriate in the final audit, the patient at the window It consists of a series of flows such as providing the drug to As an example of such a drug provision service, each task shown in FIG. ”, ”dispensing”, ”final audit”, and ”drug delivery accounting”. Some of these operations can proceed independently of each other.
In this embodiment, the output of the drug information document is performed during the work of "pharmaceutical delivery accounting". For example, among the tasks that make up the drug delivery service, the pharmacy receptionist receives prescription information at the "reception", and the pharmacist among the people in charge receives "patient information collection", "dispensing", and "drug delivery accounting". "Medical history confirmation", "prescription audit", "dispensing design", "medication explanation", "dispensing decision", and "final audit" are performed. , the drug information document is output. In the operation of "pharmaceutical delivery accounting", the drug information document created by outputting the drug information is delivered to the patient when the pharmacist delivers the drug.

[Configuration of drug information output device 10]
The drug information output device 10 of the present invention is a device that is used by a person in charge of each task that constitutes drug provision work.

The drug information output device 10 is intended to provide multifaceted support for drug delivery operations in pharmacies, and includes a control unit 11 that performs various arithmetic processing and a storage unit 12 that stores various information, as well as a keyboard and a touch panel. It is a general-purpose personal computer provided with an input unit 13 and a display unit 14 realized by, for example, a display. The drug information output device 10 is connected to the printing machine 20 by wire or wirelessly. Various programs are installed in such a medication information output device 10, and the controller 11 operates according to these programs to perform a medication information output function unique to the present invention in addition to a receipt computer function and a medication history management function. Demonstrate. When the person in charge inputs prescription information from the input unit 13 to the drug information output device 10, the drug information output function detects a change between the received prescription information and the past prescription information, and detects the changed points. This is a function to output specified drug information data.

It should be noted that to output means to output drug information data from the drug information output device to a device other than the drug information output device. In addition, it includes displaying drug information on the display unit 14 such as a display, and transmitting drug information data to another terminal through a wired or wireless communication line.
In addition, a drug information document is a document containing explanations that will serve as a reference when taking a drug, which is delivered together with the drug at the pharmacy when the drug is delivered. It includes a sheet of paper with a description, a sticker, and a medicine bag containing medicine. "Pharmaceutical information" refers to explanatory information that serves as a reference when taking drugs described in the pharmaceutical information document.

[Functional Configuration of Medication Information Output Device 10]
Next, the functional configuration of the medication information output device 10 for exerting the medication information output function will be described with reference to FIG.
FIG. 2 is a schematic diagram showing the functional configuration of the medication information output device 10. As shown in FIG. In exerting the drug information output function, the control unit 11 of the drug information output device 10 includes a prescription reception unit 111, a drug change identification unit 112, a change type identification unit 113, a usage change identification unit 114, and a drug information output unit. 115 work. Further, the storage unit 12 is provided with a prescription database 121 and a medicine database 122 .

The prescription receiving unit 111 receives prescription information from the input unit 13 as prescription information. The prescription reception unit 111 stores information on the received prescription in the prescription database 121 .
Specifically, the prescription reception unit 111 receives a prescription from a patient by a pharmacy receptionist who is in charge of the window, inputs the contents of the prescription from the input unit 13, and receives information on the prescription. The prescription reception unit 111 stores the information of the received prescription in the prescription database 121 in association with the reception date and time and the information identifying the patient.
It should be noted that the reception of prescription information may take various forms. For example, an image of a prescription may be obtained from a scanner and the prescription information may be received based on the obtained image, or a wired or wireless communication line may be used. may be accepted by receiving prescription information via

Here, the prescription database 121 will be described with reference to FIG.
FIG. 3 is a schematic diagram illustrating storage contents of the prescription database 121. As shown in FIG. The prescription database 121 is a database that stores information on received prescriptions, and is used for the receipt computer function and the medication history management function. It is used in the identification unit 114 to identify changes in drugs.
The prescription database 121 includes a prescription ID that identifies a prescription, information that identifies a patient, reception date that indicates the date and time when the prescription was received, prescription medicine that indicates the medicine described in the prescription, and when the prescription medicine was received. Memorize the dosage, which indicates how much to take.

Returning to FIG. 2, the drug change identification unit 112 identifies a change in the drug by comparing prescription information received by the prescription receiving unit 111 and prescription information for a predetermined period in the past.
Specifically, based on the information of the prescription received by the prescription receiving unit 111, the drug change specifying unit 112 stores the information of the prescription for the past predetermined period associated with the patient who is the target of the prescription in the prescription database. 121. Then, the drug change specifying unit 112 specifies a change in the drug in the prescription information received by the prescription receiving unit 111 and the extracted prescription information for the past predetermined period.

For example, when the prescription receiving unit 111 receives a prescription for patient "A" on December 15, the drug change identifying unit 112 extracts information on a prescription corresponding to the prescription ID "001001" from the prescription database 121. do. The prescription information corresponding to the prescription ID "001001" is the prescription information for the past one month associated with the patient "A" for whom the received prescription is received. Then, the drug change specifying unit 112 compares the received prescription information (E tablet, F tablet, C capsule, D tablet) with the past prescription information (A tablet, B tablet, C tablet, D tablet). addition of E tablet, F tablet, and C capsule to the prescription and removal of A tablet, B tablet, and C tablet from the prescription are identified as changes in the drug.

Further, for example, when the prescription receiving unit 111 receives a prescription for patient “Hei” on December 15, the drug change specifying unit 112 stores information on the prescription corresponding to the prescription ID “001003” in the prescription database 121. Extract from The prescription information corresponding to the prescription ID "001003" is the prescription information for the past one month associated with the patient "Hei" who is the target of the received prescription. Then, the drug change identification unit 112 compares the received prescription information (A tablet, B tablet, G tablet) with past prescription information (A tablet, B tablet, C tablet), and determines that the G tablet is the prescription. to specify as a change that the C tablet has been removed from the prescription.

In addition, the past predetermined period is a period in which the patient can fully recognize that there was a change in the prescription and fix it in the memory, and it is desired to clearly indicate the change in the prescription to the patient. In this embodiment, one month's worth of prescription information is extracted.

The change type identification unit 113 classifies the drug change identified by the drug change identification unit 112 into change types.
Specifically, the change type identification unit 113 refers to the drug database 122 for the change in the drug identified by the drug change identification unit 112, and refers to the drug information (brand name, non-proprietary name, therapeutic category name, efficacy/effect, etc.). ) is extracted, and when the extracted drug information is common, the added drug and the removed drug are associated with each other, and the change type is classified according to the presence or absence of the association and the content of the association.

Here, the drug change type refers to a type indicating how the drug change in the prescription is displayed in the drug information. In this embodiment, the drug change types are "change" in which the added drug and the removed drug are associated, and "addition" in which the added drug and the removed drug are not associated. Categorized as "delete". "Change" means "change of dosage form" where the brand name is the same but the dosage form is different between the drug to which the contents of the correspondence are added and the drug which is removed, and the brand name is different between the drugs. , “generic change” where the generic name is the same, and “ingredient change” where the brand name and generic name are different but the therapeutic class name or indication is the same.

For example, if E tablet, F tablet, and C capsule are added to the prescription and A tablet, B tablet, and C tablet are removed from the prescription as a change in the drug, the brand name is the same and the dosage form is the same. Different C capsules and C tablets are referred to as "change" and "dosage form change". E tablet and A tablet, which have different brand names but the same generic name, are referred to as "change" and "generic change." In addition, F tablet and B tablet, which have different brand names and nonproprietary names but have the same therapeutic category name, are referred to as "change" and "ingredient change."

That is, the change type identifying unit 113 associates the added medicine with the excluded medicine, and identifies the added medicine that was not associated, the excluded medicine that was not associated, or the added medicine that was associated. A combination of a drug added and a drug excluded is classified as either “added”, “deleted” or “changed”. Then, when the combination of the added drug and the excluded drug is classified as "change", the change type specifying unit 113 further assigns " "change of dosage form", "change of generic name" when the brand name and non-proprietary name are the same among drugs, "change of ingredients" when the brand name and non-proprietary name are different but the therapeutic category name or indication is the same ”.

Here, the drug database 122 will be described with reference to FIG.
FIG. 4 is a schematic diagram illustrating the storage contents of the drug database 122. As shown in FIG. The drug database 122 is a database that stores information about drugs, and is mainly composed of information derived from package inserts issued by drug providing companies. The drug database 122 is used when the change type specifying unit 113 classifies the change type of the drug, and is also used to refer to the drug information output by the drug information output unit 115, for example.
The drug database 122 includes a drug ID that identifies a drug, a brand name that indicates the brand name of the drug, a generic name that indicates the general name of the ingredients of the drug, and an efficacy classification that indicates what kind of efficacy the drug has. It stores the name and efficacy/effect indicating what kind of disease the drug is effective for.

Returning to FIG. 2, the usage change specifying unit 114 compares the prescription information received by the prescription receiving unit 111 with the prescription information for a predetermined period in the past, and finds that there has been a change in the usage and dose of the same drug. Identify things.
Specifically, based on the information of the prescription received by the prescription receiving unit 111, the usage change specifying unit 114 stores the information of the prescription for a predetermined past period associated with the patient who is the target of the prescription in the prescription database. 121. Then, the usage change specifying unit 114 specifies that there has been a change in the usage and dose of the same drug in the prescription information received by the prescription receiving unit 111 and the extracted prescription information for the predetermined past period. .

For example, when the prescription receiving unit 111 receives a prescription for patient "Otsu" on December 15, the usage change specifying unit 114 extracts information on a prescription corresponding to the prescription ID "001002" from the prescription database 121. do. The prescription information corresponding to the prescription ID "001002" is the prescription information for the past one month associated with the patient "Otsu" who is the target of the received prescription. Then, the drug change specifying unit 112 obtains the received prescription information (tablet A (1st in the morning), tablet B (2nd in the morning, 2nd in the afternoon, 2nd in the evening), tablet C (1st in the morning, 1st in the evening), tablet D (1st in the morning, 1st in the afternoon, 1st in the evening) 1)) and past prescription information (A tablet (1 morning), B tablet (1 morning, 1 evening), C tablet (1 morning, 1 evening), D tablet (1 morning, 1 afternoon, 1 evening)) to specify that the dosage and administration of tablet B changed from "1 in the morning, 1 in the evening" to "2 in the morning, 2 in the afternoon, and 2 in the evening."

The medication information output unit 115 outputs medication information in different representation formats based on the specified change in the prescription. Specifically, the drug information output unit 115 outputs drug information data including a drug change display indicating that the drug has been changed or a dosage and administration change display indicating that the dosage and administration has been changed based on the specified change in the prescription. Generate. The drug information output unit 115 outputs data based on the generated drug information data. It has become.

[Processing of drug information output device 10]
Next, the processing of the medicine information output device 10 will be described with reference to FIG.
FIG. 5 is a schematic diagram showing the flow of processing of the drug information output device 10. As shown in FIG.
The processing of the drug information output device 10 is started when the receptionist of the pharmacy receives a predetermined operation for starting the processing. When the processing of the drug information output device 10 is started, the prescription reception unit 111 of the drug information output device 10 receives the prescription information from the receptionist of the pharmacy inputting the prescription information from the input unit 13. (Step S1). The prescription receiving unit 111 stores the received prescription information in the prescription database 121 (step S2).

Subsequent to step S2, the drug change identifying unit 112 of the medication information output device 10 retrieves information on past prescriptions associated with the patient for whom the prescription received by the prescription receiving unit 111 in step S1 from the prescription database 121. Extract (step S3). Then, the drug change specifying unit 112 specifies a change in the drug in the prescription information received by the prescription receiving unit 111 and the extracted prescription information for the predetermined past period (step S4).

Subsequently, the change type identifying unit 113 confirms whether the drug change identifying unit 112 has identified a change in the drug. The process proceeds to step S6. Further, the change type identification unit 113 confirms whether or not the drug change identification unit 112 has identified a change in the drug, and if the drug change identification unit 112 has not identified a change in the drug, the change type is not classified. Then, the process proceeds to step S7 (step S5).
Then, when the drug change identification unit 112 identifies a change in the drug, the change type identification unit 113 refers to the drug database 122 to obtain drug information (brand name, generic name, therapeutic category name, efficacy/effect, etc.). to extract The change type identification unit 113 associates the added drug with the removed drug when the extracted drug information is common, and classifies the change type according to the presence or absence of the association and the contents of the association (step S6).

Subsequently, the usage change specifying unit 114 compares the prescription information received by the prescription receiving unit 111 with the prescription information for a predetermined period in the past, and determines that there has been a change in the usage and dose of the same drug. Identify (step S7).

Subsequently, the drug information output unit 115 generates drug information data including a drug change display indicating that the drug has been changed or a dosage and administration change display indicating that the dosage and administration has been changed based on the change in the specified prescription. (Step S8).

Here, a drug information document output based on the drug information data generated by the drug information output unit 115 will be described as an example.
FIG. 6 exemplifies a drug document output based on drug information data generated when a drug is associated with an accepted prescription and a past prescription when a change occurs in the drug. It is a diagram.
The drug information document has V1, which is a column where the description and photo of the delivered drug is shown, and V2, which is a column where the drug and dosage before the change occurs, and V2, which shows the dosage and administration of the drug. V3, which is a column.

V1 includes columns E1, F1, and C1, which show names, descriptions, and photographs of E-tablet, F-tablet, and C-capsule, respectively. The description is composed of a part relating to a general description of the drug extracted from the drug database 122 and a different part for each change type explaining the details of the change. For example, the explanation in column E1 consists of a general explanation, "This is a cholesterol-lowering drug..." and a general explanation, "This is an inexpensive drug with the same ingredients as tablet A." It consists of a part explaining the contents of the change.

Also, the part explaining the content of the change differs for each change type. For example, in column E1, an explanation corresponding to the change type of "generic change" is generated as "cheap medicine with the same ingredients as tablet A." The explanation corresponding to the change type of "generic change" consists of the name of the previous drug and a description indicating that the ingredients are the same and the price is low.
For example, in the F1 column, an explanation corresponding to the change type of "ingredient change" is generated as "This medicine is more effective than tablet B." The explanation corresponding to the change type of "ingredient change" consists of the name of the previous drug and a description indicating that there is a difference in efficacy or safety.
For example, in column C1, an explanation corresponding to the change type of "Change dosage form" is generated as "From tablet to capsule." The explanation corresponding to the change type of "ingredient change" is composed of descriptions indicating the dosage form of the conventional drug and the dosage form of the present drug.

V2 is shown in a clear position when column A1 showing a photograph of A tablet, which is an excluded drug, corresponding to E tablet shown in E1 corresponds to E1, and corresponds to F tablet shown in F1. Column B1, which shows a photograph of tablet B, which is an excluded drug, is shown in a clear position corresponding to F1, and shows a photograph of tablet C, which is an excluded drug corresponding to C capsule shown in C1. Correspondence between column C2 and column C1 is shown at a clear position, so that changes in drugs are shown clearly.

V3 indicates the dosage and administration of E-tablet, F-tablet, C-capsule and D-tablet. In column V3, how much medicine should be taken in the morning, noon, and evening is shown in order from the left column. For example, in column V3, the row for tablet D indicates that one tablet should be taken in the morning, one tablet in the afternoon, and one tablet in the evening.

FIG. 7 shows a conventional drug information document (FIG. 7(1)) delivered when the present invention is not applied when delivering the drug shown in FIG. 6, and the drug shown in FIG. It is a figure which illustrates the pharmaceutical information document (FIG. 7 (2)) issued at the time of the previous visit of delivery.
The pharmaceutical information document shown in FIG. 7(1) shows the medicines to be delivered (E tablet, F tablet, C capsule, D tablet) and explains each medicine. However, the drug information document in FIG. 7(1) cannot be grasped at a glance how the patient has changed from the previous drug. Therefore, even if the patient was able to take the drug habitually, the drug changed, and the patient could not grasp the correspondence relationship between the drug that was habitually taken and the drug that was newly taken. , you may forget to take or take the wrong dose.
Then, when the patient tries to grasp how the drug changed when the drug changed, the drug information document issued this time shown in FIG. 7 (1) and the drug information document issued last time shown in FIG. Changes in drugs could not be grasped without comparison with drug information documents. In addition, even if the patient compares the drug information document issued this time shown in FIG. 7(1) with the drug information document issued last time shown in FIG. If you do not compare the explanations such as "A tablet" and "E tablet", you may forget to take the medicine or take the wrong medicine. Specifically, in the case of generic change or ingredient change, the patient's physical condition may be affected by taking the remaining drug before the prescription change and the drug after the prescription change. Sometimes.
Therefore, as in the present invention, there is a need to easily output drug information that allows patients to easily grasp changes in drug delivery status. The output drug information functions as a tool for proper use of drugs.

FIG. 8 shows a drug information document output based on drug information data generated when a drug change occurs in an accepted prescription and a past prescription and the drug is not associated. FIG. 4 is a diagram illustrating an example;
The G1 column shows an explanation and a photograph of the added drug G tablet, and the G2 column displaying "new" indicating that it is newly added is shown.
In addition, in column C3, tablet C, which is an excluded drug, is displayed, and column C3 is indicated with an X so that it is clear that there is no drug corresponding to tablet C that is excluded. there is

FIG. 9 is a diagram exemplifying a pharmaceutical information document output based on pharmaceutical information data generated when a change in dosage and administration occurs between an accepted prescription and a past prescription.
Column B2 shows the dosage and administration of tablet B, indicating that 2 tablets should be taken in the morning, 2 tablets in the afternoon, and 2 tablets in the evening.

Returning to FIG. 5, the drug information output unit 115 outputs based on the generated drug information data (for example, printed by the printer 20) (step S9), and ends the process.

In the present embodiment, the drug information document printed in step S9 is configured as a drug bag, which is a bag for containing the drug when delivering the drug.
Specifically, in the present embodiment, the pharmaceutical information document is a rectangular sheet, and a vertical dashed line is printed in the center of the sheet. The drug information document has a display area where drug information including a drug change indication indicating that the drug has been changed or a dosage and administration change indication indicating that the dosage and administration has been changed is displayed on either side bounded by a dashed line. is provided. On the back side of the side on which the dashed lines and drug information are displayed, adhesive application portions are printed on the four peripheral edges.
Such a drug packet configured as a drug bag is folded into mountain folds along the dashed line and adhered by applying an adhesive to the adhesive application portion to form a bag shape. Drugs corresponding to the drug information are stored in the drug information sheet configured as a drug bag, and delivered to the patient by the person in charge of the pharmacy.

The present embodiment has been described above. According to such a drug information output device 10, drug change display (A1, B1, C2, G2, etc.) indicating that the drug has been changed based on the change between the prescription information and the past prescription information Alternatively, it is possible to easily output drug information with a dosage and administration change display (B2, etc.) indicating that the dosage and administration has changed, so that the patient can easily grasp the change in the delivery status of the drug. Become.

In addition, according to the medication information output device 10, when the change includes the added drug and the removed drug, the added drug and the removed drug are associated, and which drug changes to which drug. Since the drug information is automatically reflected in the drug information, it is possible to easily output the drug information containing the drug change display, and the patient can easily grasp the change in the delivery status of the drug. .

In addition, according to the medication information output device 10, when the change includes the added drug and the removed drug, the added drug and the removed drug are associated to change the dosage form, generic change, or It is possible to easily output the drug information indicating that the drug corresponds to any of the ingredients, so that the patient can easily grasp what changes have occurred in the drug.

Although the embodiments of the present invention have been described above, the present invention is not limited to the above-described embodiments. Moreover, the effects described in the present embodiment are merely enumerations of the most suitable effects resulting from the present invention, and the effects of the present invention are not limited to those described in the present embodiment.

In addition, in the present embodiment, the drug information is configured as a medicine bag, but the present invention is not limited to this as long as an area for displaying the drug information is provided. Alternatively, it may be a sticker having an adhesive-applied surface on the side opposite to the side on which the drug information is displayed.

In the present embodiment, the drug change identification unit 112 extracts one month's worth of prescription information as a past predetermined period. If so, the period is not limited to one month, and an appropriate period may be set as appropriate.
In addition, such a past predetermined period may be set to a different period for each patient or drug. For example, elderly patients generally take longer to fully recognize changes in drugs, so a longer period of time may be used. A period of 6 months may be set, and drugs for acute diseases are generally taken for a short period of time and become habitual, and it does not take time to fully recognize changes in drugs, so a shorter period may be set for a period of two weeks.

Further, in the present embodiment, the drug information including either the drug change display indicating that the drug has been changed or the dosage and administration change display indicating that the dosage and administration has been changed was exemplified, but the drug information output unit 115 The pharmaceutical information to be output is not limited to this, and may include both a drug change display and a dosage and administration change display. In order to include both the drug change display and the dosage and administration change display, the drug information output unit 115 outputs both the drug change display and the dosage and administration change display so that the ratio of the drug change display and the dosage and administration change display to the drug information does not become too large. The change display may be reduced and displayed.

Also, the present invention can be applied to a terminal device having the functional configuration shown in FIG. At this time, having the functional configuration shown in FIG. Including possible states. That is, the present invention can also be applied to so-called ASP services that provide business applications to customers via the Internet.

The series of processes described above can be executed by hardware or by software.
In other words, the functional configuration of FIG. 2 is merely an example and is not particularly limited. That is, it is sufficient for the computer to have a function capable of executing the above-described series of processes as a whole, and what kind of functional block is used to realize this function is not particularly limited to the example in FIG.
Also, one functional block may be composed of hardware alone, software alone, or a combination thereof.

When a series of processes is to be executed by software, a program constituting the software is installed in a computer or the like from a network or a recording medium.
The computer may be a computer built into dedicated hardware. The computer may also be a computer capable of executing various functions by installing various programs, such as a general-purpose personal computer.

10 drug information output device 11 control unit 111 prescription reception unit 112 drug change identification unit 113 change type identification unit 114 usage change identification unit 115 drug information output unit 12 storage unit 121 prescription database 122 drug database 13 input unit 14 display unit 20 printer

Claims (5)

A drug information output device for outputting drug information data provided by a pharmacist to a patient in a dispensing pharmacy and displaying it on a display unit or printing it on a drug information document,
identifying means for identifying a change in medication based on a change between information in a patient's prescription and information in a prescription older than the prescription;
A drug change display indicating that a drug has been changed based on the identification by the identifying means, the drug change display including a display explaining details of the change from the drug before the change to the drug after the change. drug information output means for outputting the drug information data including and displaying it on the display unit or printing it on the drug information document;
with
The specifying means further specifies a change type indicating a type of change of the drug,
The drug information output means makes the description of the content of the change a description corresponding to the change type specified by the specifying means.
A drug information output device characterized by: When the type of change specified by the specifying unit is a type of change to a drug with a different dosage form, the medication information output means adds the dosage form of the drug before the change to the explanation of the content of the change. Include content that indicates the dosage form after change,
The drug information output device according to claim 1, characterized in that: When the type of change specified by the specifying unit is a type of change to a generic drug, the drug information output means indicates that the price is different from the drug before the change in the description of the content of the change. include content,
3. The drug information output device according to claim 1 or 2, characterized in that: When the type of change specified by the specifying unit is a type of change to a drug with a different component, the drug information output means adds the drug before the change and the effect or safety to the explanation of the details of the change. include content that indicates gender differences;
The drug information output device according to any one of claims 1 to 3, characterized in that: A program for controlling a computer constituting a drug information output device that outputs drug information data provided by a pharmacist to a patient in a dispensing pharmacy and displays it on a display unit or prints it on a drug information document,
a specific function that identifies a medication change based on a change between information in a patient's prescription and information in a prescription that predates the prescription;
A drug change display indicating that a drug has been changed based on the specification by the specifying function, the drug change display including a display explaining the details of the change from the drug before the change to the drug after the change. a drug information output function that outputs the drug information data including
on the computer,
The specifying function further specifies a change type indicating a change type of the drug,
The drug information output function sets the description of the content of the change as a description corresponding to the change type specified by the specific function .
A program characterized by

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