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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Detalles Bibliográficos
Autores principales: Huang, Jing, Zhang, Xinyuan, Du, Jingcheng, Duan, Rui, Yang, Liu, Moore, Jason H., Chen, Yong, Tao, Cui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153695/
https://www.ncbi.nlm.nih.gov/pubmed/29295353

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153695/
https://www.ncbi.nlm.nih.gov/pubmed/29295353

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