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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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Bibliografski detalji
Izdano u:Br J Clin Pharmacol
Glavni autori: Bailey, Chantelle, Peddie, David, Wickham, Maeve E., Badke, Katherin, Small, Serena S., Doyle‐Waters, Mary M., Balka, Ellen, Hohl, Corinne M.
Format: Artigo
Jezik:Inglês
Izdano: John Wiley and Sons Inc. 2016
Teme:
Online pristup: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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