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The Impact of Litigation-Associated Reports on Signal Identification in the US FDA's Adverse Event Reporting System
Monica A Muñoz1, Gerald J Dal Pan2
1Office of Surveillance and Epidemiology, Center for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, MD, USA. monica.munoz@fda.hhs.gov.
Drug Safety
|May 18, 2019
Abstract
No abstract available in PubMed .
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