Active Postmarketing Drug Surveillance for Multiple Adverse Events
Abstract
Postmarketing drug surveillance is the process of monitoring the adverse events of pharmaceutical or medical devices after they are approved by the appropriate regulatory authorities. Historically, such surveillance was based on voluntary reports by medical practitioners, but with the widespread adoption of electronic medical records and comprehensive patient databases, surveillance systems that utilize such data are of considerable interest....
Paper Details
Title
Active Postmarketing Drug Surveillance for Multiple Adverse Events
Published Date
Dec 1, 2015
Journal
Volume
63
Issue
6
Pages
1528 - 1546
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Notes
History