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Standardizing adverse drug event reporting data

BACKGROUND: The Adverse Event Reporting System (AERS) is an FDA database providing rich information on voluntary reports of adverse drug events (ADEs). Normalizing data in the AERS would improve the mining capacity of the AERS for drug safety signal detection and promote semantic interoperability be...

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Autors principals: Wang, Liwei, Jiang, Guoqian, Li, Dingcheng, Liu, Hongfang
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2014
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4142531/
https://ncbi.nlm.nih.gov/pubmed/25157320
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2041-1480-5-36
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