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Characterizing drug-related adverse events by joint analysis of biomedical and genomic data: A case study of drug-induced pulmonary fibrosis

Spontaneous reporting systems such as the FDA’s adverse event reporting system (FAERS) present a great resource to mine for and analyze real-world medication usage. Our study is based on a central premise that FAERS captures unsuspected drug-related adverse events (AEs). Since drug-related AEs resul...

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Detalles Bibliográficos
Autores principales: Jiang, Alex, Jegga, Anil G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Medical Informatics Association 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5961825/
https://www.ncbi.nlm.nih.gov/pubmed/29888048