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Comparative evaluation of adverse drug reaction reporting forms for introduction of a spontaneous generic ADR form

Despite comprehensive and stringent phases of clinical trials and surveillance efforts, unexpected and serious adverse drug reactions (ADRs) repeatedly occur after the drug is marketed. ADR reporting is an important aspect of an efficient and effective pharmacovigilance program. Although Medwatch, Y...

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Detalles Bibliográficos
Autores principales: Singh, Anshi, Bhatt, Parloop
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3487270/
https://www.ncbi.nlm.nih.gov/pubmed/23129957
http://dx.doi.org/10.4103/0976-500X.99417

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