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Discovering adverse drug events combining spontaneous reports with electronic medical records: a case study of conventional DMARDs and biologics for rheumatoid arthritis

The use of multiple data sources has been preferred in the surveillance of adverse drug events due to shortcomings of using only a single source. In this study, we proposed a framework where the ADEs associated with interested drugs are systematically discovered from the FDA’s Adverse Event Reportin...

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Detalhes bibliográficos
Publicado no:AMIA Jt Summits Transl Sci Proc
Main Authors: Wang, Liwei, Rastegar-Mojarad, Majid, Liu, Sijia, Zhang, Huaji, Liu, Hongfang
Formato: Artigo
Idioma:Inglês
Publicado em: American Medical Informatics Association 2017
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5543355/
https://ncbi.nlm.nih.gov/pubmed/28815115
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