A curated and standardized adverse drug event resource to accelerate drug safety research

Identification of adverse drug reactions (ADRs) during the post-marketing phase is one of the most important goals of drug safety surveillance. Spontaneous reporting systems (SRS) data, which are the mainstay of traditional drug safety surveillance, are used for hypothesis generation and to validate...

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Detalles Bibliográficos
Autores principales: Banda, Juan M., Evans, Lee, Vanguri, Rami S., Tatonetti, Nicholas P., Ryan, Patrick B., Shah, Nigam H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Data Descriptor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4872271/
https://www.ncbi.nlm.nih.gov/pubmed/27193236
http://dx.doi.org/10.1038/sdata.2016.26

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4872271/
https://www.ncbi.nlm.nih.gov/pubmed/27193236
http://dx.doi.org/10.1038/sdata.2016.26

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