Variability in the assessment of adverse events in a multicenter clinical trial
- 1 December 2001
- journal article
- Published by Elsevier BV in Clinical Therapeutics
- Vol. 23 (12), 2011-2020
- https://doi.org/10.1016/s0149-2918(01)80153-3
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Evaluation of Safety Data from Controlled Clinical Trials: The Clinical Principles ExplainedDrug Information Journal, 2000
- Spontaneous reporting of adverse drug reactions: who reports and what?Pharmacoepidemiology and Drug Safety, 1998
- Buprenorphine maintenance treatment of opiate dependence: a multicenter, randomized clinical trialAddiction, 1998
- Geographical variation in adverse event reporting rates in clinical trialsPharmacoepidemiology and Drug Safety, 1997
- Under-reporting of adverse drug reactions in the elderlyPharmacoepidemiology and Drug Safety, 1995
- Adverse drug reactions: Comparison of two report methodsPharmacoepidemiology and Drug Safety, 1994
- Causality assessment of suspected adverse drug reactions: A transatlantic viewPharmacoepidemiology and Drug Safety, 1992
- Role and place of causality assessmentPharmacoepidemiology and Drug Safety, 1992
- Reliability and Validity of Judgments Concerning Adverse Events Suffered by Hospitalized PatientsMedical Care, 1989
- A method for estimating the probability of adverse drug reactionsClinical Pharmacology & Therapeutics, 1981