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System and method for improving adverse reaction reporting rate of clinical drugs

A technology of adverse reactions and drugs, applied in the field of medical systems, can solve problems such as inaccurate evaluation results of adverse drug reactions, untimely reporting time, large data differences, etc., so as to avoid low enthusiasm for reporting, timely reporting, and solve omissions high yield effect

Pending Publication Date: 2021-01-12
WENZHOU PEOPLES HOSPITAL
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  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] At present, the adverse reaction evaluation of drugs after marketing is mainly reported by medical institutions and drug manufacturers. Adverse reaction reports have a high rate of missed reports, large data discrepancies, and untimely reporting, etc.
Differences in reported data make the evaluation results of adverse drug reactions inaccurate

Method used

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  • System and method for improving adverse reaction reporting rate of clinical drugs
  • System and method for improving adverse reaction reporting rate of clinical drugs

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Embodiment Construction

[0030] In the description of the present invention, it should be noted that the terms "center", "upper", "lower", "left", "right", "vertical", "horizontal", "inner", "outer" etc. The indicated orientation or positional relationship is based on the orientation or positional relationship shown in the drawings, or the orientation or positional relationship that is usually placed when the product of the invention is used, and is only for the convenience of describing the present invention and simplifying the description, rather than indicating or implying References to devices or elements must have a specific orientation, be constructed and operate in a specific orientation and therefore should not be construed as limiting the invention. In addition, the terms "first", "second", "third", etc. are only used for distinguishing descriptions, and should not be construed as indicating or implying relative importance.

[0031] In the description of the present invention, it should also ...

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Abstract

The invention relates to the technical field of medical systems, in particular to a system and method for improving the adverse reaction report rate of clinical drugs. The system comprises a login module used for allowing a user to login the system, a report form filling module used for filling a report form after login, a report form viewing module used for viewing the filled report form, a database module used for storing related data including login information data and report table information data, a scoring module used for scoring the filled report form so as to enable a related user toobtain scores according to the scores and used for evaluating the filled report form and allowing the user to change the report form subsequently and obtain more points after the change, and a creditexchange module used for exchanging commodities or services by using the credits. The invention has the beneficial effects that by simplifying the process and awarding mechanism of the report form, the interest of the masses and all institutions in reporting the adverse reaction report form is stimulated, and the problem that the report missing rate of adverse reaction reports is high is solved.

Description

technical field [0001] The invention relates to the technical field of medical systems, in particular to a system and method for improving the reporting rate of clinical adverse drug reactions. Background technique [0002] Adverse Drug Reactions (ADR) refer to various reactions that are not related to the purpose of medication and are not conducive to patients due to the effect of the drug itself or the interaction between drugs during the use of commonly used doses of drugs. With the development of the pharmaceutical market and the increasing number of new drug varieties, it is gradually becoming more difficult for the public to use drugs correctly. Unsafe drug use is difficult to completely avoid in the world, and ADR monitoring is the main means of drug safety monitoring. Carrying out ADR monitoring is conducive to understanding the occurrence of ADR, facilitating timely adoption of safety precautions, and preventing the expansion of the scope of ADR hazards. [0003] A...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): G16H70/40G16H10/20G06Q30/02G06Q10/06G06Q50/26
CPCG16H70/40G16H10/20G06Q30/0208G06Q10/06395G06Q50/26
Inventor 杨金招熊建华吴煜
Owner WENZHOU PEOPLES HOSPITAL
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