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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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Detalles Bibliográficos
Autores principales: Wang, Liwei, Rastegar-Mojarad, Majid, Liu, Sijia, Zhang, Huaji, Liu, Hongfang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Medical Informatics Association 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5543355/
https://www.ncbi.nlm.nih.gov/pubmed/28815115