JP5902737B2 - Medicine bag as a tool for proper use of medicines - Google Patents

Description

The present invention also relates to a medicine bag medicine information is displayed.

Conventionally, when a patient brings a prescription issued from a hospital / clinic to a pharmacy, the pharmacy issues the drug described in the prescription to the patient and issues a pharmacy document describing the explanation of the drug to be delivered Sometimes.
In order for a pharmacy to create such a drug information document, with the recent development of information processing technology, information processing technology has been introduced, and a pharmacy person in charge uses a computer with a database that stores descriptions and photos of drugs. When prescription information is entered into a computer, the computer creates a medical information document regarding the prescription drug. Such a medical information document is useful for a patient to grasp information on a medicine including how to take the medicine.
For example, Patent Document 1 discloses a creation system that prints a medicine instruction book in which a calendar indicating a use time and a use amount of a medicine is described in addition to a name and a photograph of the medicine delivered.

JP 2001-47773 A

  However, it has been difficult to grasp such changes in the drug instruction book (medical information document) even if there has been a change in the delivery contents of the medicine and the delivery contents of the current medicine in the past. .

  Then, an object of this invention is to enable it to grasp | ascertain easily the change of the delivery content of a chemical | medical agent.

  In order to achieve the above object, a medicine bag of one embodiment of the present invention is a medicine bag configured to form a bag by adhering a predetermined portion of a rectangular paper, and containing a medicine. In the area, a display area for displaying drug information including a drug change display indicating that the drug has been changed or a dosage change display indicating that the dosage has been changed is provided. An adhesive attachment portion indicating a region where the adhesive is attached is provided on the peripheral portion.

  In order to achieve the above object, a pharmaceutical information output apparatus according to an aspect of the present invention includes a prescription storage unit that stores information on a patient's prescription, and information between the prescription information and prescription information that is earlier than the prescription. And a medicinal information output means for outputting medicinal data including a medicinal change display indicating that the medicinal substance has been changed or a dosage change indication indicating that the medicinal dosage has been changed.

  In order to achieve the above object, a program according to one aspect of the present invention stores a prescription information of a patient, and based on a change between the prescription information and prescription information past the prescription, Generating a drug information including a drug change display indicating that the drug has changed or a dosage change display indicating that the dosage has been changed.

  According to the present invention, it becomes possible to easily grasp a change in the delivery contents of a medicine.

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

  Embodiments of the present invention will be described below with reference to the drawings.

An application scene of a medical information document output by the medical information output device 10 of the present invention will be described with reference to FIG.
FIG. 1 is a conceptual diagram showing a medicine providing service in a pharmacy. FIG. 1 (1) shows the flow of each work, and FIG. 1 (2) shows the contents of each work.
Referring to FIG. 1 (1), the drug provision service receives a prescription from the patient at the window, dispenses the drug according to the prescription, and if the final audit confirms that the dispensing is appropriate, the patient at the window It is constituted by a series of flows such as providing the drug. Such a drug providing operation includes, as an example, each of the operations shown in FIG. 1 (2), that is, "reception", "medicine history confirmation", "prescription audit", "patient information collection", "dispensing design", "explanation concerning medication", "dispensing decision""Dispensing""Finalaudit""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 at the time of the “drug delivery accounting” operation. For example, among the tasks that make up the drug provision work, the pharmacy receptionist receives prescription information at the "reception", and among the persons in charge, the pharmacist performs "patient information collection""dispensing""drug delivery accounting" After confirming that there is no problem in delivering prescription drugs after confirming drug history, prescribing audit, dispensing design, explanation of medication, dispensing decision, and final audit, In pharmacy information is output. In the “medicine delivery accounting” operation, the medication information document created by the output of medication information is delivered by the pharmacist to the patient as well as the medication.

[Configuration of Drug Information Output Device 10]
The medicinal information output device 10 of the present invention is a device used by a person in charge of each work constituting a medicine providing business.

  The drug information output device 10 is intended to provide multifaceted support for drug provision work in a pharmacy, and includes a keyboard 11 and a touch panel in addition to a control unit 11 that performs various arithmetic processes and a storage unit 12 that stores various information. A general-purpose personal computer including an input unit 13 and a display unit 14 using a display. The medicine information output apparatus 10 is connected to the printing machine 20 by wire or wirelessly. Such a drug information output apparatus 10 has various programs installed therein, and the control unit 11 operates according to these programs, so that the drug information output function unique to the present invention is added to the receipt control function and the drug history management function. Demonstrate. When the person in charge inputs prescription information from the input unit 13 to the medicinal information output device 10, the medicinal information output function detects a change between the accepted prescription information and the past prescription information, and identifies the changed point. It is a function that outputs the data of the specified drug information.

Note that outputting means that the drug information data is output from the drug information output device to a device other than the drug information output device, and the drug information is printed on the printing machine 20 based on the drug information data to create a drug document. In addition, the information includes displaying the drug information on the display unit 14 such as a display or transmitting the data of the drug information to another terminal through a wired or wireless communication line.
In addition, the pharmacy information document refers to a document that contains explanations that can be used as reference when taking a drug that is delivered with the drug when the drug is delivered at the pharmacy. This includes a sheet of paper, a seal and a medicine bag containing medicine. Medicinal information refers to explanatory information for reference when taking a drug described in a drug information document.

[Functional configuration of pharmaceutical information output apparatus 10]
Next, the functional configuration of the drug information output device 10 for exhibiting the drug information output function will be described with reference to FIG.
FIG. 2 is a schematic diagram showing a functional configuration of the medicine information output apparatus 10. In demonstrating the drug information output function, the control unit 11 of the drug information output device 10 includes a prescription receiving unit 111, a drug change specifying unit 112, a change type specifying unit 113, a usage change specifying unit 114, and a drug information output unit. 115 function. The storage unit 12 is provided with a prescription database 121 and a drug database 122.

The prescription receiving unit 111 receives prescription information from the input unit 13 as prescription information. The prescription receiving unit 111 stores the received prescription information in the prescription database 121.
Specifically, in the prescription receiving unit 111, a person in charge of reception at a pharmacy who is in charge of a window receives a prescription from a patient, inputs the contents of the prescription from the input unit 13, and receives prescription information. The prescription receiving unit 111 stores the received prescription information in the prescription database 121 in association with the reception date and information specifying the patient.
The reception of prescription information may take various forms. For example, a prescription image may be acquired from a scanner, and prescription information may be received based on the acquired image, or a wired or wireless communication line It 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 the stored contents of the prescription database 121. The prescription database 121 is a database that stores information on received prescriptions. The prescription database 121 is used for a receipt control function and a drug history management function. In the drug information output function, a drug change specifying unit 112 and a usage change described later are used. In the identification part 114, it is used in order to identify the change of the medicine.
The prescription database 121 includes a prescription ID for specifying a prescription, information for specifying a patient, a reception date indicating the date and time when the prescription is received, a prescription drug indicating a drug described in the prescription, and when the prescription drug is Memorize the dosage to indicate how much you will take.

Returning to FIG. 2, the medicine change specifying unit 112 compares the prescription information received by the prescription receiving unit 111 with the prescription information for a predetermined period in the past, and specifies a change in the medicine.
Specifically, the medicine change specifying unit 112 stores prescription information for a predetermined past period associated with the patient who is the subject of the prescription based on the prescription information received by the prescription receiving unit 111. Extract from 121. Then, the medicine change specifying unit 112 specifies a change in medicine in the prescription information received by the prescription receiving unit 111 and the extracted prescription information for a predetermined past period.

  For example, when the prescription receiving unit 111 receives a prescription for the patient “A” on December 15, the medicine change specifying unit 112 extracts prescription information corresponding to the prescription ID “001001” from the prescription database 121. To do. The prescription information corresponding to the prescription ID “001001” is prescription information for the past one month associated with the patient “former” that is the subject of the accepted prescription. Then, the medicine change specifying unit 112 compares the received prescription information (E lock, F lock, C capsule, D lock) with the past prescription information (A lock, B lock, C lock, D lock). Thus, the E tablet, the F tablet, and the C capsule are added to the prescription, and the change in the medicine is specified that the A tablet, the B tablet, and the C tablet are removed from the prescription.

  Further, for example, when the prescription receiving unit 111 receives a prescription for the patient “日 に” on December 15, the medicine change specifying unit 112 displays prescription information corresponding to the prescription ID “001003” as the prescription database 121. Extract from The prescription information corresponding to the prescription ID “001003” is prescription information for the past month associated with the patient “丙” that is the subject of the accepted prescription. Then, the medicine change specifying unit 112 compares the received prescription information (A tablet, B tablet, G tablet) with the past prescription information (A tablet, B tablet, C tablet), and the G tablet is prescription. And identifies as a change that C-tablet has been removed from the prescription.

  The past predetermined period is a period in which the patient can fully recognize that there has been a change in the prescription and can be fixed in memory, and a period in which it is desirable to clearly indicate the change in the prescription to the patient, In this embodiment, prescription information for one month is extracted.

The change type specifying unit 113 classifies the change of the drug specified by the drug change specifying unit 112 into the change type.
Specifically, the change type specifying unit 113 refers to the drug database 122 for drug changes specified by the drug change specifying unit 112 (sales name, general name, drug classification name, efficacy / effect, etc.). ) And the added medicine and the removed medicine are associated with each other when the extracted medicine information is common, and the change type is classified for each presence / absence of association and the contents of the association.

  Here, the change type of the medicine refers to a type indicating how the change of the medicine in the prescription is displayed in the medicine information. In the present embodiment, the change type of the medicine includes “change” in which the added medicine and the removed medicine are associated with each other, and “addition” in which the added medicine and the removed medicine are not associated with each other. Classified as “deleted”. “Change” means “drug type change” in which the sales name is the same and the dosage form is different between the drug to which the content of the correspondence is added and the removed drug, and the sales name is different between the drugs. The generic name is the same, “generic change”, the sales name and the generic name are different, and the medicinal effect classification name or the efficacy / effect is the same, “classification change”.

  For example, when E tablets, F tablets, and C capsules are added to the prescription, and A tablet, B tablet, and C tablet are removed from the prescription, the sales name is the same and the dosage form is Different C capsules and C tablets are referred to as “change” and “drug form change”. In addition, the E name and the A name, which have different sales names among drugs and have the same general name, are referred to as “change” and “generic change”. Also, the sales name and the general name are different, and F tablets and B tablets having the same medicinal effect classification name are referred to as “change” and “component change”.

  That is, the change type identification unit 113 associates the added medicine with the excluded medicine, adds the medicine that is not associated, the excluded medicine that is not associated, or the associated added medicine. The combination of the excluded drug and the excluded drug is classified into one of “addition”, “deletion”, and “change”. When the combination of the added medicine and the excluded medicine is classified as “changed”, the change type specifying unit 113 further sets the correspondence when the sales name is the same and the dosage form is different. `` Change in dosage form '', `` Generic change '' when sales names differ between drugs and general names are the same, `` Generic change '' when sales names and general names are different, and drug names or efficacy / effects are the same `` Change ingredients '' ".

Here, the drug database 122 will be described with reference to FIG.
FIG. 4 is a schematic view illustrating the stored contents of the drug database 122. The drug database 122 is a database that stores information related to drugs, and is mainly composed of information derived from a package insert issued by a pharmaceutical provider. The drug database 122 is used when the change type specifying unit 113 classifies the change type of the drug, and is used for referring to the drug information output by the drug information output unit 115.
The drug database 122 includes a drug ID that identifies a drug, a sales name that indicates the sales name of the drug, a general name that indicates a general name related to a component of the drug, and a medicinal effect classification that indicates what drug the drug has. The name is memorized including the efficacy and 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 there has been a change in the dosage of the same medicine. Identify that.
Specifically, the usage change specifying unit 114, based on the prescription information received by the prescription receiving unit 111, stores prescription information for a predetermined past period associated with the subject patient of the prescription. Extract from 121. Then, the usage change specifying unit 114 specifies that there has been a change in the dosage of the same medicine in the prescription information received by the prescription receiving unit 111 and the extracted prescription information for a predetermined past period. .

  For example, the usage change specifying unit 114 extracts prescription information corresponding to the prescription ID “001002” from the prescription database 121 when the prescription receiving unit 111 receives the prescription of the patient “B” on December 15. To do. The prescription information corresponding to the prescription ID “001002” is prescription information for the past month associated with the patient “B” who is the subject of the accepted prescription. Then, the medicine change specifying unit 112 receives information on the received prescription (A lock (morning 1), B lock (morning 2 noon 2 evening 2), C lock (morning 1 evening 1), D lock (morning 1 noon 1 evening) 1)) and past prescription information (A lock (morning 1), B lock (morning 1 evening 1), C locking (morning 1 evening 1), D locking (morning 1 noon 1 evening 1))) Then, it is specified that the dosage of the B tablet has changed from “morning 1 evening 1” to “morning 2 noon 2 evening 2”.

  The medicinal information output unit 115 outputs medicinal information in different expression formats based on the change in the specified prescription. Specifically, the drug information output unit 115 stores drug information data including a drug change display indicating that the drug has been changed based on the change in the specified prescription or a dosage change display indicating that the dosage has been changed. Generate. The drug information output unit 115 performs output based on the generated drug information data. For example, the drug information output unit 115 outputs the drug information data to the printer 20 for printing. It has become.

[Processing of Drug Information Output Device 10]
Then, with reference to FIG. 5, the process of the pharmaceutical information output apparatus 10 is demonstrated.
FIG. 5 is a schematic diagram showing a processing flow of the medicine information output apparatus 10.
The process of the pharmacy information output device 10 is started when a person in charge at the pharmacy receives a predetermined operation for starting the process. When the process is started, the prescription accepting unit 111 of the medicinal product output device 10 accepts the prescription information when the person in charge of the pharmacy inputs 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 specifying unit 112 of the drug information output device 10 obtains information on past prescriptions associated with the prescription target received by the prescription receiving unit 111 in step S1 from the prescription database 121. Extract (step S3). Then, the medicine change specifying unit 112 specifies a change in medicine in the prescription information received by the prescription receiving unit 111 and the extracted prescription information for a predetermined past period (step S4).

Subsequently, the change type specifying unit 113 confirms whether or not the drug change specifying unit 112 has specified a change in the drug. If the drug change specifying unit 112 has specified a change in the drug, the change type specifying unit 113 classifies the change type. The process proceeds to step S6. Further, the change type specifying unit 113 confirms whether or not the drug change specifying unit 112 has specified a change in the drug, and if the drug change specifying unit 112 has not specified a change in the drug, the change type is not classified. Then, the process proceeds to step S7 (step S5).
Then, the change type specifying unit 113 refers to the drug database 122 when the drug change specifying unit 112 specifies a change in the drug (sales name, general name, drug category name, efficacy / effect, etc.). To extract. The change type specifying 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 / absence of the association and the content 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 confirms that there has been a change in usage dose for the same medicine. Specify (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 based on the specified change in the prescription or a dosage change display indicating that the dosage has been changed. (Step S8).

Here, an explanation will be given of an example of a medicine information document output based on the medicine information generated by the medicine information output unit 115.
FIG. 6 exemplifies a drug document that is output based on drug information data that is generated when a drug change occurs between a received prescription and a past prescription and the drug is associated with the prescription. FIG.
The medical information document shows V1 which is a column where a description and a photograph of a drug to be delivered are shown, V2 which is a column where a drug / usage dose before the change occurs, and a drug usage dose. And V3 which is a column.

  V1 includes the E1 column, the F1 column, and the C1 column, and names, explanations, and photographs regarding the E lock, the F lock, and the C capsule, respectively, are shown. The explanation is composed of a part relating to a general explanation of the medicine extracted from the medicine database 122 and a part different for each change type explaining the content of the change. For example, in the explanation of the E1 column, there is a part related to the general explanation that “It is a drug that lowers cholesterol.” And “A cheap drug with the same ingredients as A tablet”. It consists of a part that explains the content of the change.

Moreover, the part explaining the content of a change differs for every change classification. For example, in the E1 column, a description corresponding to the change type of “generic change” is generated as “It is an inexpensive medicine of the same component as the A tablet”. The explanation corresponding to the change type of “generic change” is composed of the name of the conventional drug and a description indicating that the ingredients are the same and the price is low.
For example, in the F1 column, a description corresponding to the change type of “component change” is generated as “it is a medicine that is more effective than the B tablet”. The explanation corresponding to the change type of “component change” is composed of a description indicating that there is a difference in the effect or safety from the name of the previous drug.
For example, in the C1 column, a description corresponding to the change type of “change in dosage form” is generated as “It changed from a tablet to a capsule.” The explanation corresponding to the change type of “component change” is composed of a description showing the dosage form of the conventional medicine and the dosage form of the present medicine.

  V2 is shown in a clear position when the A1 column showing the picture of the A tablet which is an excluded drug corresponding to the E tablet shown in E1 corresponds to E1, and corresponds to the F tablet shown in F1 The B1 column showing a photograph of the excluded B tablet corresponding to F1 is shown in a clear position corresponding to F1, and a photograph of the excluded C tablet corresponding to the C capsule shown in C1 is shown. When the C2 column corresponds to C1, it is shown in a clear position, and the change of the drug is shown clearly.

  V3 indicates the dosage of E, F, C, and D tablets. In the column V3, the amount of medicine taken in the morning, noon and evening is shown in order from the left column. For example, in the V3 column, the row of D lock indicates that one tablet in the morning, one tablet in the daytime, and one tablet in the evening should be taken.

FIG. 7 shows a conventional medicine information document (FIG. 7 (1)) to be delivered when the medicine shown in FIG. 6 is delivered and the present invention is not applied, and the medicine shown in FIG. It is a figure which illustrates the medicine information document (Drawing 7 (2)) delivered at the time of the last visit of grant.
The medicine information document shown in FIG. 7 (1) shows medicines to be delivered (E tablets, F tablets, C capsules, D tablets), and the respective medicines are described. However, the medication information document in FIG. 7 (1) cannot grasp at a glance how the patient has changed from the previous medication. Therefore, even if the patient was able to take the drug habitually, the drug changed, and the patient was unable to grasp the correspondence between the drug he was taking habitually and the newly taken drug. , You may forget to drink or take the wrong dose.
Then, when the patient tries to grasp how the medicine has changed, the medicine information document issued this time as shown in FIG. 7 (1) and the last time issued as shown in FIG. 7 (2) are issued. The change in the drug could not be grasped without comparing it with the drug information document. In addition, even if the patient compares the drug information document issued this time as shown in FIG. 7 (1) with the drug information document issued last time as shown in FIG. If you do not compare the explanations such as "", you may not know whether the A lock has changed to the E lock, and you may forget to take it or take it incorrectly. Specifically, in the case of generic changes or ingredient changes, the patient's physical condition is modulated by the patient taking the remaining medicine 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 a patient to easily grasp changes in the delivery status of drugs. The outputted drug information functions as a tool for proper use of the drug.

FIG. 8 shows a medicinal information document output based on medicinal data generated when there is a change in medicine between the received prescription and the past prescription and the medicine is not associated. It is a figure illustrated.
In the G1 column, explanations and photos of the added G-tablet, which is a drug, are shown, and a G2 column displaying “new” indicating that it has been newly added is shown.
In addition, the C3 column is displayed with the excluded C drug, and the C3 column is displayed as x so that it is clear that there is no drug corresponding to the excluded C tablet. Yes.

FIG. 9 is a diagram exemplifying a medication information document that is output based on the medication information that is generated when a change in dosage occurs between the accepted prescription and the past prescription.
Column B2 shows the dosage of B tablet and indicates that two tablets in the morning, two tablets in the day, and two tablets in the evening should be taken.

  Returning to FIG. 5, the medicine information output unit 115 performs output based on the generated medicine information data (for example, printed on the printing machine 20) (step S <b> 9), and ends the process.

In the present embodiment, the medicine information document printed in step S9 is configured as a medicine bag that is a bag for storing medicine when the medicine is delivered.
Specifically, in the present embodiment, the drug information document is a rectangular sheet, and a vertical broken line is printed at the center of the sheet. The drug information document has a display area for displaying drug information including a drug change display indicating that a drug has been changed or a dosage change display indicating that a dosage has been changed on any surface with a broken line as a boundary. Is provided. And the adhesive attachment part is printed in the four peripheral parts on the back surface of the surface where the broken line and the medicine information are displayed.
Such drug information configured as a medicine bag is folded in a mountain fold with a broken line as a boundary, and is bonded to each other by providing an adhesive at an adhesive attachment portion, thereby forming a bag shape. The medicine information document configured as a medicine bag stores medicine corresponding to the medicine information and is delivered to the patient from the person in charge at the pharmacy.

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

  Moreover, according to the medicine information output device 10, when the medicine added to the change and the medicine removed are included, the medicine added is associated with the medicine removed, and which medicine changes to which medicine. The drug information with the drug change indication can be output easily and the patient can easily grasp the change in the delivery status of the drug. .

  Further, according to the medicine information output device 10, when the medicine added to the change and the removed medicine are included, the added medicine and the removed medicine are associated with each other, and the dosage form change, generic change or It is possible to easily output drug information indicating that it corresponds to one of the components, and it is possible to easily grasp what kind of drug the patient has changed.

  As mentioned above, although embodiment of this invention was described, this invention is not restricted to embodiment mentioned above. Further, the effects described in the present embodiment are merely a list of the most preferable effects resulting from the present invention, and the effects of the present invention are not limited to those described in the present embodiment.

  Further, in this embodiment, the drug information is configured as a drug bag, but is not limited to this as long as an area for displaying drug information is provided. For example, the drug information is a sheet on which only drug information is printed. It may be a seal in which an adhesive application surface is provided on the surface opposite to the surface on which the drug information is displayed.

In the present embodiment, the medicine change specifying unit 112 extracts prescription information for one month as a predetermined period in the past, but the period during which the patient can sufficiently recognize the change in the prescription. If so, it is not limited to one month, and an appropriate period may be set as appropriate.
In addition, such a predetermined period may be set differently for each patient or drug. For example, an elderly patient generally takes a long time to fully recognize a change in drug, so that it is longer. A period of 6 months may be set, and drugs for acute diseases generally have a habit of taking less time, and it takes less time to fully recognize changes in the drug. A period of 2 weeks may be set.

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

  Further, 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. 2 means that in addition to installing software that realizes the functional configuration in the terminal device, the terminal device uses the software installed in a predetermined server via the network. Includes possible states. That is, the present invention can also be applied to a so-called ASP service that provides business applications to customers through the Internet.

The series of processes described above can be executed by hardware or can be executed 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 that the computer has a function capable of executing the above-described series of processes as a whole, and what functional block is used to realize this function is not particularly limited to the example of FIG.
In addition, one functional block may be constituted by hardware alone, software alone, or a combination thereof.

When a series of processing is executed by software, a program constituting the software is installed on a computer or the like from a network or a recording medium.
The computer may be a computer incorporated in dedicated hardware. The computer may be a computer capable of executing various functions by installing various programs, for example, a general-purpose personal computer.

DESCRIPTION OF SYMBOLS 10 Pharmaceutical information output apparatus 11 Control part 111 Prescription reception part 112 Drug change specific part 113 Change classification specific part 114 Usage change specific part 115 Pharmaceutical information output part 12 Storage part 121 Prescription database 122 Drug database 13 Input part 14 Display part 20 Printing machine

Claims (1)

A medicine bag for storing medicine, which is configured in a bag shape by adhering a predetermined portion of rectangular paper,
In one area of the paper, there is provided a display area for displaying drug information including a drug change display indicating that the drug has been changed or a dosage change display indicating that the dosage has been changed,
An adhesive attachment part indicating an area for attaching an adhesive to the four peripheral edges of the back surface provided with the one area is provided,
A medicine bag, characterized by

Images