Cargando…
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...
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: | |
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 |
Ejemplares similares
-
A time-indexed reference standard of adverse drug reactions
por: Harpaz, Rave, et al.
Publicado: (2014) -
DrugMechDB: A Curated Database of Drug Mechanisms
por: Gonzalez-Cavazos, Adriana Carolina, et al.
Publicado: (2023) -
A reference set of clinically relevant adverse drug-drug interactions
por: Kontsioti, Elpida, et al.
Publicado: (2022) -
A standard database for drug repositioning
por: Brown, Adam S., et al.
Publicado: (2017) -
A curated gene and biological system annotation of adverse outcome pathways related to human health
por: Saarimäki, Laura Aliisa, et al.
Publicado: (2023)