Evaluating Drug Risk Using GAN and SMOTE Based on CFDA’s Spontaneous Reporting Data

Adverse drug reactions (ADRs) pose health threats to humans. Therefore, the risk re-evaluation of post-marketing drugs has become an important part of the pharmacovigilance work of various countries. In China, drugs are mainly divided into three categories, from high-risk to low-risk drugs, namely,...

Full description

Bibliographic Details
Main Authors: Jianxiang Wei, Guanzhong Feng, Zhiqiang Lu, Pu Han, Yunxia Zhu, Weidong Huang
Format: Article
Language:English
Published: Hindawi Limited 2021-01-01
Series:Journal of Healthcare Engineering
Online Access:http://dx.doi.org/10.1155/2021/6033860