Adverse drug event reporting systems: a systematic review

AIM: Adverse drug events (ADEs) are harmful and unintended consequences of medications. Their reporting is essential for drug safety monitoring and research, but it has not been standardized internationally. Our aim was to synthesize information about the type and variety of data collected within AD...

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Detaylı Bibliyografya
Yayımlandı:Br J Clin Pharmacol
Asıl Yazarlar: Bailey, Chantelle, Peddie, David, Wickham, Maeve E., Badke, Katherin, Small, Serena S., Doyle‐Waters, Mary M., Balka, Ellen, Hohl, Corinne M.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: John Wiley and Sons Inc. 2016
Konular:
Systematic Reviews
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4917803/
https://ncbi.nlm.nih.gov/pubmed/27016266
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bcp.12944
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