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Published in 2018 at "Pharmacoepidemiology and Drug Safety"
DOI: 10.1002/pds.4651
Abstract: Estimating the rate of adverse events (AEs) caused by a treatment in clinical trials typically involves comparing the proportions of patients experiencing AEs in intervention and control groups. However, potentially important information, including duration, recurrence,…
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Keywords:
events oseltamivir;
study;
psychiatric adverse;
prophylaxis trials ... See more keywords