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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Detalles Bibliográficos
Autores principales: Wang, Liwei, Jiang, Guoqian, Li, Dingcheng, Liu, Hongfang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4142531/
https://www.ncbi.nlm.nih.gov/pubmed/25157320
http://dx.doi.org/10.1186/2041-1480-5-36

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4142531/
https://www.ncbi.nlm.nih.gov/pubmed/25157320
http://dx.doi.org/10.1186/2041-1480-5-36

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