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Post-Approval Drug Safety Surveillance

Following the drug-approval process, concerns remain regarding the safety of new drugs that are introduced into the marketplace. In the case of rare adverse events, the number of subjects that are treated in randomized controlled trials is invariably inadequate to determine the safety of the new pha...

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Autores principales: Gibbons, Robert D., Amatya, Anup K., Brown, C. Hendricks, Hur, Kwan, Marcus, Sue M., Bhaumik, Dulal K., Mann, J. John
Formato: Artigo
Lenguaje:Inglês
Publicado: 2010
Materias:
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC2841706/
https://ncbi.nlm.nih.gov/pubmed/20070192
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1146/annurev.publhealth.012809.103649
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