Exploring the FDA Adverse Event Reporting System (FAERS) to Generate Hypotheses for Disease Monitoring

The FDA Adverse Event Reporting System (FAERS) is a database for post-marketing drug safety monitoring and influences FDA safety guidance documents, such as changes in drug labels. The number of cases in the FAERS has rapidly increased with the improvement of submission methods and data standard and...

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Detalhes bibliográficos
Main Authors: Fang, Hong, Su, Zhenqiang, Wang, Yuping, Miller, Aaron, Liu, Zhichao, Howard, Paul, Tong, Weida, Lin, Simon M
Formato: Artigo
Idioma:Inglês
Publicado em: 2014
Assuntos:
Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4194268/
https://ncbi.nlm.nih.gov/pubmed/24448476
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/clpt.2014.17
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