Marketed drug information standardization method and device, server and storage medium

Abstract

The embodiment of the invention relates to a marketed drug information standardization method and device, a server and a computer readable storage medium. The method comprises the following steps: collecting drug standard data from drug standards; carrying out structured processing on the collected drug standard data to form structured drug standard data; collecting drug data, wherein the drug data comprises a drug name and an approval document number; matching the acquired drug data in the structured drug standard data; and in the case of successful matching, automatically retrieving a drug specification corresponding to the drug data on a network, and storing the acquired drug data and the acquired drug specification in association in corresponding entries in a structured drug information database. Therefore, the invention provides the method for collecting and providing standardized marketed drug information more quickly and comprehensively.

Description

technical field [0001] The present disclosure relates to the technical field of drug information standardization, and more specifically, to a method, device, server, and computer-readable storage medium for standardizing drug information on the market. Background technique [0002] With China's accession to the International Human Drug Registration Technical Coordination Conference (ICH), China's drug registration technical requirements have been fully integrated with international standards. China's drug R&D and registration are also fully entering the era of globalization, which requires higher standardization of drug information, not only to meet domestic use in China, but also to connect with existing international standards. On the other hand, relevant standardized information such as the composition, dosage form, indications, and classification of drugs is also the basis for realizing clinical auxiliary drug decisions. [0003] Existing methods for standardizing drug ...

AI Technical Summary

Problems solved by technology

Therefore, the workload of collecting all the drug instructions is huge

[0005] (2) Incomplete coverage of drug instructions

The number of drug insert sheets collected and provided to the public by existing drug information standardization manufacturers is limited. At present, the most complete data provider (such as Yaozhi.com) has only 77,000 records. Excluding records of different time versions and insert sheet templates, it is estimated that there are only 30,000 There are about 100 drugs, and high coverage of all drug information cannot be guaranteed

[0006] (3) Drug instructions are hysteresis

Drug instructions can only be collected publicly after the drug has been on the market for a period of time, and this uncertain lag makes it difficult to regularly collect and update data

[0007] (4) Data quality cannot be guaranteed

According to our data research, the quality of manuals in text form cannot be guaranteed, and often each website copies each other

The number of image formats is relatively small, and the release date span is very large

[0008] (5) Drug information is incomplete

In addition, the drug composition information in the drug instructions lacks dosage and units, which brings great limitations to the application of subsequent drug information

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