JP2008310574A - Side effect information management system, side effect information management method, side effect information management program - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a side effect information management system by which side effect information can be efficiently transmitted from a medical institution to a pharmaceutical company. <P>SOLUTION: The side effect information management system includes: a side effect information registration means which, when side effect information including information specifying a suspect drug and necessity information indicating whether or not the notification to a pharmaceutical company is required are input in the medical institution's terminal, receives the side effect information and the necessity information from the medical institution's terminal and registers both information in a database. The system also includes a side effect information reference means which, when it has received a transmission request including information specifying a pharmaceutical company from a pharmaceutical company's terminal, extracts side effect information in which a medicine sold by the pharmaceutical company that has transmitted the transmission request is the suspect drug, and of which notification is required, from the database, and transmits it to the pharmaceutical company's terminal. <P>COPYRIGHT: (C)2009,JPO&INPIT

Description

  The present invention relates to a technique for sharing information about prescription drugs among related parties such as doctors and pharmaceutical companies, and more particularly to a technique for sharing side effect information of prescription drugs.

  When a doctor examines a patient or a pharmacist gives medication instructions, it is necessary to know the prescription drug history and side effect information of the patient. However, sharing of patient prescription drug history and side effect information between medical institutions and pharmacies is not sufficient. For this reason, each time a patient visits a different medical institution, he / she is often asked whether he / she has taken a drug in the past or caused side effects, or whether he / she is currently taking any medicine. In many cases, patients cannot accurately grasp such information, and in such a case, accurate information cannot be transmitted to a doctor or a pharmacist.

  There is also a method to manage such information using a medicine notebook issued by a pharmacy, but since there is no habit of carrying it and it is issued for each pharmacy, management becomes complicated, so a medicine notebook is issued However, it may be difficult for patients to convey accurate information to medical institutions.

  In most cases, side effect information is transmitted from each medical institution to the pharmaceutical company, and the information is transmitted from the doctor to the medical information staff of the pharmaceutical company, and the medical information staff communicates it to the department in charge of the company. It is thought that the information transmission becomes inefficient through the use of a human hand.

  Patent Document 1 describes a medicine information registration inquiry server that manages medicine prescription contents for each user in a unified manner. This medicine information registration inquiry server accumulates in a database personal information of a user (patient) input by a user terminal and information on a prescription medicine. And according to the inquiry request | requirement of the persons concerned, such as a patient person and a doctor, these information is transmitted to a user terminal. When registering and inquiring information, authorization is managed by authenticating with a UserID and password.

  Patent Document 2 describes a disease state estimation database that assists a pharmacist in presuming a patient's disease state and making a pharmaceutical diagnosis of a prescribed drug. This pathological condition estimation database is composed of a prescription database, a drug database, and a disease database, and these databases can be searched in association with each other. The prescription database stores prescription examples of prescriptions issued in the past. In the drug database, the actions, side effects, interactions, and types of wounds and diseases to be applied are stored in association with each prescription drug. The injury and illness database stores medication conditions and precautions for each injury and illness.

JP 2002-288343 A JP 2004-185196 A

  In each of the above technologies related to the present invention, the pharmaceutical company cannot obtain information directly from the medical institution in which the side effect information is generated, and the information transmission is not efficient.

  Therefore, an object of the present invention is to provide a side effect information management system that can efficiently transmit side effect information from a medical institution to a pharmaceutical company.

  The side effect information management system of the present invention provides side effect information and necessary information when side effect information including information for identifying a suspected drug and necessity information indicating the necessity of contacting a pharmaceutical company are input to a medical institution terminal. The side effect information registration means for receiving sex information from a medical institution terminal and registering this information in a database, and the pharmaceutical that transmitted the transmission request when receiving a transmission request including information identifying the pharmaceutical company from the pharmaceutical company terminal The drug sold by the company is a suspected drug, and side effect information reference means for extracting side effect information that needs to be contacted from a database and transmitting it to a pharmaceutical company terminal is provided.

  According to the present invention, side effect information can be efficiently transmitted from a medical institution to a pharmaceutical company.

The configuration and operation of the side effect information management system 5 according to one embodiment of the present invention will be described with reference to the drawings.
As shown in FIG. 1, the side effect information management system 5 is connected to a pharmacy terminal 1, a medical institution terminal 2, a pharmaceutical company terminal 3, and a patient terminal 4 via a network 6.

  The pharmacy terminal 1 is a terminal device used by a pharmacist or the like who provides a prescription drug to a patient according to a prescription issued by a doctor, and is, for example, a personal computer having a communication function. The pharmacist uses the pharmacy terminal 1 to refer to the prescription drug history registered in the side effect information management system 5 and confirms that the medicine described in the prescription brought by the patient is unprescription. In addition, side effect information is referred to and used for patient advice.

  The medical institution terminal 2 is a terminal device used by a medical institution related person such as a doctor who examines a patient and issues a prescription if necessary, and is a personal computer having a communication function, for example. The doctor registers the prescription data and the side effect data in the side effect information management system 5 using the medical institution terminal 2 when examining the patient. In addition, the doctor refers to prescription drug history information and side effect information regarding the patient under examination using the medical institution terminal 2.

  The pharmaceutical company terminal 3 is a terminal device used by an employee of a pharmaceutical company that manufactures and sells medicines, and is, for example, a personal computer having a communication function. The employee refers to the side effect information and prescription number information of the medicine manufactured and sold by the company using the pharmaceutical company terminal 3.

  The patient terminal 4 is a terminal device used by a patient who receives a medical prescription, and is, for example, a personal computer or a mobile phone having a communication function. Using the patient terminal, the patient refers to his / her prescription drug history and side effect information of the medicine he / she has prescribed.

FIG. 2 is a functional block diagram of the side effect management system 5.
The side effect management system 5 includes an interface unit 10 that transmits / receives data to / from each terminal device of FIG. 1 and registers / reads information to / from the database unit 20 and a database unit 20 that stores and manages the database.
The database unit 20 includes databases of a user master 21, a patient master 22, a medical institution master 23, a pharmacy master 24, a pharmaceutical company master 25, a product master 26, prescription drug history information 27, side effect information 28, and prescription number information 29. Manage memory. Each of the above databases is implemented as, for example, a relational database including one or more tables.

In the user master 21, identification information, passwords, and usage classifications of all users are registered. Usage classification codes are information indicating whether a user belongs to a medical institution, pharmacy, pharmaceutical company, or patient. The functions that can be used by each user are controlled by the usage classification code, and information disclosure is restricted to protect personal information. I do.
For example, a doctor can refer to a prescription drug history only for a patient that he / she has prescribed (control for each item), and a patient can be authenticated by using a health insurance card number and can only refer to his / her data ( The pharmaceutical company performs control such that the prescription drug history information 27 linked with the patient master 22 is not accessible (control for each table).

  An embodiment of access control is shown in FIG. In this figure, “◎” indicates that users belonging to the usage category shown in the “user” column have the authority to input and refer to the information. Similarly, “◯” indicates that only the reference authority is provided, and “×” indicates that neither the input authority nor the reference authority is provided. The authority for the side effect information by patient of the medical institution is “「 ”, but the authority is only given to the information regarding the logged-in user, that is, the patient being examined.

The patient master 22 is a database that stores information about the patient such as name and age.
The medical institution master 23 is a database that stores information related to medical institutions such as a name, an address, and an e-mail address for receiving a notification mail.
The pharmacy master 24 is a database that stores information about pharmacies such as names and addresses.
The pharmaceutical company master 25 is a database that stores information on a pharmaceutical company such as a name and an address.
The product master 26 is a database that stores information on medicines such as names and manufacturing companies.

  The prescription drug history information 27 includes the name of the prescription drug, the prescription amount, the prescription date, information about the prescribed patient, information about the medical institution that issued the prescription, and the like.

  The side effect information 28 includes information on the content of the side effect, such as the suspected drug, the severity, and the onset date.

  The prescription number information 29 is information obtained by counting the number of prescriptions for each medicine.

  The interface unit 10 includes an authentication unit 11, a history information registration reference unit 12, a prescription number information registration reference unit 13, a side effect information registration reference unit 14, a notification mail transmission unit 15, and a usage restriction unit 16.

The authentication unit 11 authenticates a user who uses the side effect information management system 5. User authentication is performed, for example, based on whether or not the password received from each terminal matches the password extracted from the user master 21 using the received user identification information as a search key. As the user identification information, a health insurance card number is used for patients, and a user ID set for each user in advance is used for other users.
Note that the authentication information and the authentication method are not limited to the above example. For example, challenge-response authentication may be used, or biological information such as a fingerprint may be used instead of a password.

  The history information registration reference unit 12 registers the prescription drug history information and prescription information received from the pharmacy terminal 1 or the medical institution terminal 2 in the prescription drug history information 27. In addition, prescription drug information and prescription information corresponding to the access authority of the user are extracted from the database unit 20 and transmitted to the pharmacy terminal 1, the medical institution terminal 2, and the patient terminal 4.

  The prescription number information registration reference means 13 counts the number of times prescribed for each prescription drug based on the prescription drug history information 27 and registers it in the prescription number information 29. Further, in response to a request from the pharmaceutical company terminal 3, the number of prescriptions for the prescription drug sold by the pharmaceutical company is extracted from the prescription number information 29 and transmitted to the requesting pharmaceutical company terminal 3.

  The side effect information registration reference means 14 registers the side effect information received from the medical institution terminal 2 in the side effect information 28. Further, side effect information corresponding to the access authority of the user is extracted from the database unit 20 and transmitted to the pharmacy terminal 1, the medical institution terminal 2, the pharmaceutical company terminal 3, and the patient terminal 4.

  The notification mail transmitting means 15 transmits an e-mail notifying the person in charge of the pharmaceutical company that new side effect information has occurred when receiving side effect information that needs to be contacted from the medical institution terminal 2 to the pharmaceutical company. . The e-mail address of the e-mail transmission destination is stored in advance for each pharmaceutical company in the pharmaceutical company master 25, for example.

  The usage restriction unit 16 manages user access authority for information stored in the database unit 20. This authority management is performed based on the use classification code extracted from the user master 21 corresponding to the user ID or health insurance card number acquired from the terminal at the time of authentication.

  Each of the above means is realized by a CPU (Central Processing Unit) of a computer constituting the side effect information management system 5 executing a computer program and controlling hardware.

  The hardware configuration of the side effect information management system 5 may be appropriately determined according to the number of users and the data amount of the database. For example, the interface unit 10 and the database unit 20 may be configured by one or a plurality of server computers, respectively, and the functions of the interface unit 10 and the database unit 20 may be mounted on one server computer.

Next, the operation of the side effect information management system 5 will be described.
FIG. 4 is a diagram showing an outline of the operation of the side effect information management system 5 when the user refers to information.
A medical institution, a pharmacy, a pharmaceutical company, and a patient log in by transmitting user identification information and a password from each terminal to the side effect information management system 5 (S1). The side effect management system 5 transmits a usage screen to each terminal, and each terminal receives the usage screen and displays it on the display device (S2).

Each user refers to the information stored in the database unit 20 within the range of authority given to the user.
The patient logs in using the health insurance card number as the user identification information, and refers to the patient information about the patient and the prescription drug history information (S3, S4).
The medical institution refers to side effect information relating to the patient being examined, and the pharmacy refers to side effect information relating to the patient attempting to purchase the prescription drug (S5).
The pharmaceutical company refers to the prescription number information of the prescription drug sold by the company (S6).

FIG. 5 is a flowchart showing the operation of the side effect information management system 5 when a user of a medical institution, for example, a doctor, refers to and inputs information.
The doctor inputs his / her user ID and password in a predetermined input field on the login screen displayed on the medical institution terminal 2. The medical institution terminal 2 transmits the user ID and password to the side effect information management system 5 (S101).

  The authentication means 11 of the side effect information management system 5 receives the user ID and password, and authenticates the user based on these information and authentication information stored in advance in the database unit 20. If the authentication means 11 determines that the user attempting to log in is not a legitimate user, the user is prompted to retransmit the user ID and password (No in S102, S101).

  When the authentication unit 11 determines that the user who is attempting to log in is a valid user, the history information reference unit 12 sends necessary information for displaying the usage screen, for example, HTML format data, to the medical institution terminal 2. Send. The medical institution terminal 2 receives this information and displays a usage screen on the display device (Yes in S102, S103).

The doctor inputs the patient's health insurance card number and the inquiry period in a predetermined input field on the usage screen (S104). The patient enters his password. The medical institution terminal 2 transmits these pieces of information to the side effect information management system 5 (S105).
The authentication unit 11 of the side effect information management system 5 performs user authentication based on the received health insurance card number, password, and authentication information stored in the database unit 20 in advance. If the authentication unit 11 determines that the patient is not a valid user, the user is prompted to retransmit the health insurance card number and password (No in S106, S104).

When the authentication unit 11 determines that the patient is a valid user, the history information reference registration unit 12 transmits the prescription history information of the patient during the inquiry period input in S104 to the medical institution terminal 2. The medical institution terminal 2 receives this and displays it on the display device (Yes in S106, S107).
The doctor inputs prescription history data to the medical institution terminal 2 when prescribing the medicine after examining the patient. The medical institution terminal 2 transmits the prescription history data to the side effect information management system 5 (Yes in S108, S109). The history information registration reference means 12 receives prescription history data and registers it in the prescription drug history information 27. At this time, information indicating that the prescription data is not prescription (the prescription is issued but the patient has not yet purchased the prescription drug) is added.

  When there is side effect information, the doctor inputs side effect data to the medical institution terminal 2 (Yes in S108, S109). When the doctor determines that the input side effect data needs to be reported to the pharmaceutical company, for example, the doctor inputs that fact by inputting a check mark in a check box on the screen. The medical institution terminal 2 transmits the side effect data and a flag indicating the necessity of reporting to the pharmaceutical company to the side effect information management system 5 (S113). The side effect information registration reference means 14 receives these information and stores them in the side effect information 28.

  The notification mail transmission means 15 checks the flag when the side effect information is newly registered, and if the flag is turned on (indicating that notification to the pharmaceutical company is necessary), a new one is sent. An e-mail notifying that the side effect information has been registered is sent to the pharmaceutical company that sells the suspect drug. The address of the e-mail destination is registered in the pharmaceutical company master 25, for example (S114).

FIG. 6 is a flowchart showing the operation of the side effect information management system 5 when a pharmacy user, for example, a pharmacist references and inputs information.
The pharmacist inputs his user ID and password in a predetermined input field of the login screen displayed on the pharmacy terminal 1. The pharmacy terminal 1 transmits the user ID and password to the side effect information management system 5 (S201).

  The authentication unit 11 of the side effect information management system 5 performs a user authentication process in the same manner as S102 of FIG. 5, and when the authentication is successful, the pharmacy terminal 1 displays a usage screen (S202). Furthermore, the patient is authenticated in the same procedure as S104 to S106 in FIG. When the authentication is successful, the history information registration reference unit 12 extracts the history information about the patient from the prescription drug history information 27 and transmits it to the pharmacy terminal 1. This information also includes data (unprescription data) regarding an unprescription. The pharmacy terminal 1 displays the prescription drug history and the non-prescription data (S207).

  The pharmacist collates the prescription received from the patient with the displayed non-prescription data, and if the two match, the pharmacist prescribes the medicine described in the prescription and inputs the prescription data to the pharmacy terminal 1. The pharmacy terminal 1 transmits prescription data to the side effect information management system 5. The history information registration reference means 12 receives the prescription data and stores it in the prescription drug history information (208).

  The side effect information reference means 15 transmits patient side effect information to the pharmacy terminal 1. The pharmacy terminal 1 receives this and displays it on the display device (S209). The pharmacist refers to the side effect information of the patient and gives a medication instruction, and uses the product master 26 to create a medication instruction book and issue it to the patient.

  For the medicine purchased by the patient regardless of the prescription, the history information is transmitted from the pharmacy terminal 1 at the time of purchase, and the history information registration reference means 12 registers it in the database unit 20 so that the patient himself can refer to it later. Also good. In addition, the number of purchases of such drugs may be aggregated and provided to a pharmaceutical company.

FIG. 7 is a flowchart showing the operation of the side effect information management system 5 when the patient refers to information.
The patient inputs his / her health insurance card number and password in a predetermined input field on the login screen displayed on the patient terminal 4. The patient terminal 4 transmits the health insurance card number and password to the side effect information management system 5 (S301).

  The authentication means 11 of the side effect information management system 5 receives the health insurance card number and the password, and authenticates the user based on these information and authentication information stored in advance in the database unit 20. If the authentication means 11 determines that the user attempting to log in is not a valid user, the user is prompted to retransmit the health insurance card number and password (No in S302, S301).

  When the authentication means 11 determines that the user who is attempting to log in is a legitimate user, the history information registration reference means 12 indicates the prescription drug information of the logged-in patient, and the side effect information registration reference means 14 indicates the side effect information of the patient. Is transmitted to the patient terminal 4. The patient terminal 4 receives the information and displays it on the display device (Yes in S302, S303).

  As a result, patients can present their prescriptions to medical institutions and pharmacies who have not subscribed to this system by using the screen of their mobile devices. You will be able to accurately convey information about drug history and side effects.

FIG. 8 is a flowchart showing the operation of the side effect information management system 5 when the person in charge of the pharmaceutical company refers to the information.
The person in charge inputs his / her user ID and password in a predetermined input field of the login screen displayed on the pharmaceutical company terminal 3. The pharmaceutical company terminal 3 transmits the user ID and password to the side effect information management system 5 (S401).

  The authentication means 11 of the side effect information management system 5 receives the user ID and password, and authenticates the user based on these information and authentication information stored in advance in the database unit 20. If the authentication unit 11 determines that the user who is attempting to log in is not a valid user, the user is prompted to retransmit the user ID and password (No in S402, S401).

  When the authentication means 11 determines that the user who is attempting to log in is a legitimate user, the history information reference registration means 12 sends necessary information for displaying the selection screen, for example, HTML format data, to the pharmaceutical company terminal 3. Send to. The pharmaceutical company terminal 3 receives this information and displays a selection screen on the display device (Yes in S402, S403). The person in charge selects information that he / she wants to refer to.

  When the prescription number information is selected, the prescription number registration reference means 13 transmits the sales number information of the drug sold by the pharmaceutical company to which the logged-in user belongs to the pharmaceutical company terminal 3, and the pharmaceutical company terminal 3 displays this information. .

  When the side effect information is selected, the side effect information registration reference means 14 transmits the side effect information of the prescription drug sold by the pharmaceutical company to which the logged-in user belongs to the pharmaceutical company terminal 3, The pharmaceutical company terminal 3 displays this.

  Thereby, the pharmaceutical company can grasp when and at which medical institution, the doctor diagnosed the side effect for which drug. Based on this information, the pharmaceutical company conducts an internal evaluation and asks the doctor for additional information if necessary.

  Here, an example in which prescription number information and side effect information are displayed on the screen of the pharmaceutical company terminal 3 has been described. However, these pieces of information may be downloaded to the pharmaceutical company terminal 3 in a lump.

Next, the effect of the side effect information management system 5 will be described.
According to the side effect information management system 5, the side effect information registration reference unit 12 registers the side effect information in the side effect information 28 every time it receives the side effect information. The pharmaceutical company can log in to the system from the pharmaceutical company terminal 3 at any time and refer to the side effect information.
Therefore, the side effect information can be efficiently transmitted from the medical institution to the pharmaceutical company, and the pharmaceutical company can immediately know the side effect information when it occurs.

When the side effect information registration reference means 14 receives from the medical institution terminal 2 side effect information that needs to be contacted with the pharmaceutical company, it registers it in the side effect information 28 together with a flag indicating that. When such side effect information is registered, the notification mail transmitting means 15 immediately transmits an e-mail notifying that to the pharmaceutical company.
Therefore, the time required for the pharmaceutical company to know about the side effect information after it is registered can be shortened.

The side effect information registration reference means 14 transmits the side effect information of the patient in response to a request from the pharmacy terminal 1 and the medical institution terminal 2.
Therefore, doctors and pharmacists can accurately know side effect information necessary for diagnosis and dispensing.

The history information registration reference unit 12 receives a prescription drug history from the medical institution terminal 2 and registers it in the prescription drug history information 27 every time a doctor issues a prescription. The history information registration reference means 14 transmits the patient's prescription drug history information in response to requests from the pharmacy terminal 1 and the medical institution terminal 2.
Therefore, doctors and pharmacists can accurately know prescription drug history information necessary for diagnosis and dispensing. In addition, the pharmacist can compare and verify the prescription and the non-prescription data to perform accurate medication.

The history information registration reference means 12 and the side effect information registration reference means 14 transmit the patient's prescription drug history information and side effect information in response to a request from the patient terminal 4.
Therefore, the patient can present accurate prescription drug history information and side effect information to medical institutions and pharmacies that do not use this system.

The prescription number registration reference means 13 calculates the prescription number for each drug by counting the prescription drug history information 27 and registers it in the prescription number information 29. The prescription number registration reference means 13 transmits the prescription number of prescription drugs sold by the pharmaceutical company in response to a request from the pharmaceutical company terminal 3.
Therefore, the pharmaceutical company can easily grasp the latest number of prescriptions.

The usage control means 16 restricts registration and reference of information by the user based on the usage classification code registered in the user master 21.
Therefore, registration of erroneous information (for example, registration of side effect information by a patient without medical knowledge) can be prevented, and personal information of the patient can be prevented from being disclosed beyond the range necessary for diagnosis or the like.

It is a figure which shows the structure of the side effect information management system which is one Example of this invention. It is a functional block diagram of a side effect information management system. It is a figure which shows an example of the access restriction with respect to a database. It is a figure which shows the outline | summary of operation | movement of a side effect information management system. It is a figure which shows operation | movement of the side effect information management system at the time of a doctor using. It is a figure which shows operation | movement of the side effect information management system at the time of a pharmacist using. It is a figure which shows operation | movement of the side effect information management system at the time of a patient using. It is a figure which shows operation | movement of the side effect information management system at the time of using a pharmaceutical company.

Explanation of symbols

DESCRIPTION OF SYMBOLS 1 Pharmacy terminal 2 Medical institution terminal 3 Pharmaceutical company terminal 4 Patient terminal 5 Side effect information management system 6 Network 11 Authentication means 12 History information registration reference means 13 Prescription number information registration reference means 14 Side effect information registration reference means 15 Notification mail transmission means 16 Use Control means 21 User master 22 Patient master 23 Medical institution master 24 Pharmacy master 25 Pharmaceutical company master 26 Product master 27 Prescription drug history information 28 Side effect information 29 Prescription number information

Claims (18)

When the side effect information including information identifying the suspected drug and the necessity information indicating the necessity of contacting the pharmaceutical company are input to the medical institution terminal, the side effect information and the necessity information are input to the medical institution terminal. Side effect information registration means for registering these information in the database,
When a transmission request including information identifying a pharmaceutical company is received from a pharmaceutical company terminal, the drug sold by the pharmaceutical company that transmitted the transmission request is a suspected drug, and side effect information that needs to be contacted is displayed. Side effect information reference means for extracting from the database and transmitting to the pharmaceutical company terminal,
Side-effect information management system with   When the side effect information registration means receives side effect information that needs to be contacted to a pharmaceutical company, an e-mail for notifying that is sent to an e-mail address predetermined for each pharmaceutical company. The side effect information management system according to claim 1, further comprising means. History information registration means for registering the prescription drug history information in the database when receiving from the medical institution terminal prescription drug history information to be input to the medical institution terminal every time a doctor prescribes a patient;
2. The history information reference means for transmitting the prescription drug history information of a patient under examination to the medical institution terminal when receiving a transmission request from the medical institution terminal. Item 3. The side effect information management system according to Item 2.   The side effect information management system according to claim 3, wherein the history information reference unit transmits the prescription drug history information of the patient himself / herself to the patient terminal when receiving a transmission request from the patient terminal.   The said history information reference means transmits the said prescription drug history information of the patient who is going to purchase a prescription medicine to the said pharmacy terminal, when the transmission request from a pharmacy terminal is received. Side effect information management system.   When receiving the transmission request from the pharmaceutical company terminal, the prescription number information indicating the prescription quantity for each prescription drug sold by the pharmaceutical company that has transmitted the transmission request is extracted from the database, and the prescription number information is extracted from the database. The side effect information management system according to any one of claims 3 to 5, further comprising a prescription number information reference means to be transmitted to the company terminal. When the side effect information including information identifying the suspected drug and the necessity information indicating the necessity of contacting the pharmaceutical company are input to the medical institution terminal, the side effect information and the necessity information are input to the medical institution terminal. Side effect information registration step of registering these information in the database,
When a transmission request including information identifying a pharmaceutical company is received from a pharmaceutical company terminal, the drug sold by the pharmaceutical company that transmitted the transmission request is a suspected drug, and side effect information that needs to be contacted is displayed. Side effect information reference step to extract from the database and send to the pharmaceutical company terminal,
Side-effect information management method with   When receiving side effect information that requires contact with a pharmaceutical company, a notification mail transmission step is provided for sending an e-mail notifying that to a predetermined e-mail address for each pharmaceutical company. The side effect information management method according to claim 7, wherein the side effect information is managed. A history information registration step for registering the prescription drug history information in the database when receiving from the medical institution terminal prescription drug history information to be input to the medical institution terminal each time a doctor prescribes a patient;
8. A history information reference step of transmitting the prescription drug history information of a patient under examination to the medical institution terminal when receiving a transmission request from the medical institution terminal. Item 9. The side effect information management method according to Item 8.   10. The side effect information management method according to claim 9, wherein, in the history information reference step, when the transmission request from the patient terminal is received, the prescription drug history information of the patient himself / herself is transmitted to the patient terminal.   The said history information reference process WHEREIN: The said prescription drug history information of the patient who is going to purchase a prescription drug is transmitted to the said pharmacy terminal, when the transmission request from a pharmacy terminal is received. Side effect information management method.   When receiving the transmission request from the pharmaceutical company terminal, the prescription number information indicating the prescription quantity for each prescription drug sold by the pharmaceutical company that has transmitted the transmission request is extracted from the database, and the prescription number information is extracted from the database. The side effect information management method according to any one of claims 9 to 11, further comprising a prescription number information reference step to be transmitted to the company terminal. On the computer,
When the side effect information including information identifying the suspected drug and the necessity information indicating the necessity of contacting the pharmaceutical company are input to the medical institution terminal, the side effect information and the necessity information are input to the medical institution terminal. Side-effects information registration process to receive and register these information in the database,
When a transmission request including information identifying a pharmaceutical company is received from a pharmaceutical company terminal, the drug sold by the pharmaceutical company that transmitted the transmission request is a suspected drug, and side effect information that needs to be contacted is displayed. Side effect information reference processing extracted from the database and transmitted to the pharmaceutical company terminal;
Side effect information management program that executes In the computer,
When the side effect information registration process receives side effect information that needs to be contacted to a pharmaceutical company, an e-mail for notifying that is sent to an e-mail address predetermined for each pharmaceutical company. The side effect information management program according to claim 13, wherein the side effect information management program is executed. In the computer,
A history information registration process for registering the prescription drug history information in the database when receiving from the medical institution terminal prescription drug history information to be input to the medical institution terminal every time a doctor prescribes a patient;
The history information reference process of transmitting the prescription drug history information of a patient under examination to the medical institution terminal when receiving a transmission request from the medical institution terminal. Item 15. A side effect information management program according to Item 14. In the computer,
16. The side effect information management program according to claim 15, wherein, in the history information reference process, when a transmission request from a patient terminal is received, the prescription drug history information of the patient himself / herself is transmitted to the patient terminal.   The said history information reference process WHEREIN: When the transmission request | requirement from a pharmacy terminal is received, the said prescription drug history information of the patient who is going to purchase a prescription medicine is transmitted to the said pharmacy terminal. Side effect information management program. In the computer,
When receiving the transmission request from the pharmaceutical company terminal, the prescription number information indicating the prescription quantity for each prescription drug sold by the pharmaceutical company that has transmitted the transmission request is extracted from the database, and the prescription number information is extracted from the database. The side effect information management program according to any one of claims 15 to 17, wherein a prescription number information reference process to be transmitted to a company terminal is executed.

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