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Variability in the assessment of adverse events in a multicenter clinical trial

โœ Scribed by Dennis W. Raisch; William G. Troutman; Mike R. Sather; Paul J. Fudala

Book ID
117321182
Publisher
Elsevier Science
Year
2001
Tongue
English
Weight
759 KB
Volume
23
Category
Article
ISSN
0149-2918

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Although most clinical trials encompass aspects of safety, methods for assessing the safety of a drug by recording adverse events have been poorly studied. It has been suggested that adverse events rather than adverse drug reactions should be monitored, since a reliable determination of which events