The Impact of the Sentinel Initiative and FAERS Surveillance System on Consumer Safety

The U.S. Food and Drug Administration (FDA) uses the FDA Adverse Event Reporting System (FAERS) to monitor adverse events resulting from pharmaceutical drug use. However, this system has limitations such as not allowing real-time data collection. To address these limitations, the FDA launched the Se...

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Bibliographic Details
Main Author: Batra, Sonia
Format: Others
Language:en
Published: ScholarWorks 2016
Subjects:
FDA
Online Access:https://scholarworks.waldenu.edu/dissertations/2438
https://scholarworks.waldenu.edu/cgi/viewcontent.cgi?article=3541&context=dissertations