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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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Bibliografiska uppgifter
I publikationen:Br J Clin Pharmacol
Huvudupphovsmän: Bailey, Chantelle, Peddie, David, Wickham, Maeve E., Badke, Katherin, Small, Serena S., Doyle‐Waters, Mary M., Balka, Ellen, Hohl, Corinne M.
Materialtyp: Artigo
Språk:Inglês
Publicerad: John Wiley and Sons Inc. 2016
Ämnen:
Länkar: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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