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Comparing Different Adverse Effects Among Multiple Drugs Using FAERS Data

US Food and Drug Administration (FDA) Adverse Event (AE) Reporting System (FAERS) is a major source of data for monitoring drug safety. However, there is not general procedure to systematically compare drugs group. We present a statistical method, which can effectively identify significant differenc...

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Publicat a:Stud Health Technol Inform
Autors principals: Huang, Jing, Zhang, Xinyuan, Du, Jingcheng, Duan, Rui, Yang, Liu, Moore, Jason H., Chen, Yong, Tao, Cui
Format: Artigo
Idioma:Inglês
Publicat: 2017
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC8153695/
https://ncbi.nlm.nih.gov/pubmed/29295353
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