Wird geladen...

Eliciting adverse effects data from participants in clinical trials

BACKGROUND: Analysis of drug safety in clinical trials involves assessing adverse events (AEs) individually or by aggregate statistical synthesis to provide evidence of likely adverse drug reactions (ADR). While some AEs may be ascertained from physical examinations or tests, there is great reliance...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cochrane Database Syst Rev
Hauptverfasser: Allen, Elizabeth N, Chandler, Clare IR, Mandimika, Nyaradzo, Leisegang, Cordelia, Barnes, Karen
Format: Artigo
Sprache:Inglês
Veröffentlicht: John Wiley & Sons, Ltd 2018
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7098080/
https://ncbi.nlm.nih.gov/pubmed/29372930
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/14651858.MR000039.pub2
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!