Aspirin in the Food and Drug Administration Adverse Event Reporting System: Missing Demographics and Underreporting

Aspirin in the Food and Drug Administration Adverse Event Reporting System: Missing Demographics and Underreporting

Abstract Background The U.S. Food and Drug Administration (FDA) Adverse Event (AE) Reporting System (FAERS) is a global passive surveillance repository requiring mandatory updates by pharmaceutical manufacturers. Oral antiplatelet agents (OAAs) including aspirin (acetylsalicylic acid [A...

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Bibliographic Details
Main Authors: Victor L. Serebruany, Ales Tomek, Moo Hyun Kim, Oleg Litvinov, Thomas A. Marciniak
Format: Article
Language:English
Published: Georg Thieme Verlag KG 2017-07-01
Series:TH Open
Subjects:
aspirin
antiplatelet agents
adverse events
safety
registry
Online Access:http://www.thieme-connect.de/DOI/DOI?10.1055/s-0037-1606301

Internet

http://www.thieme-connect.de/DOI/DOI?10.1055/s-0037-1606301

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