Eliciting adverse effects data from participants in clinical trials

Author:

Allen Elizabeth N1,Chandler Clare IR2,Mandimika Nyaradzo1,Leisegang Cordelia1,Barnes Karen1

Affiliation:

1. University of Cape Town; Division of Clinical Pharmacology, Department of Medicine; K45, Old Main Building, Groote Schuur Hospital Observatory Cape Town Western Cape South Africa 7925

2. London School of Hygiene and Tropical Medicine; Dept of Global Health & Development; 309, 15-17 Tavistock Place London UK WC1H 9SH

Publisher

Wiley

Subject

Pharmacology (medical)

Reference103 articles.

1. How experiences become data: the process of eliciting adverse event, medical history and concomitant medication reports in antimalarial and antiretroviral trials;Allen;BMC Medical Research Methodology,2013

2. Systematic errors in the evaluation of side effects;Avery;American Journal of Psychiatry,1967

3. Relating spontaneous adverse experience reports to scores on a questionnaire querying tolerability;Barber;International Journal of Clinical Pharmacology and Therapeutics,1995

4. Unwanted effects of pentagastrin;Barrowman;Clinical Pharmacology and Therapeutics,1970

5. Brief communication: Better ways to question patients about adverse medical events: a randomized, controlled trial;Bent;Annals of Internal Medicine,2006

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