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

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 [ASA]) are broadly used...

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Detalles Bibliográficos
Autores principales: Serebruany, Victor L., Tomek, Ales, Kim, Moo Hyun, Litvinov, Oleg, Marciniak, Thomas A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Georg Thieme Verlag KG 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6524845/
https://www.ncbi.nlm.nih.gov/pubmed/31249915
http://dx.doi.org/10.1055/s-0037-1606301

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6524845/
https://www.ncbi.nlm.nih.gov/pubmed/31249915
http://dx.doi.org/10.1055/s-0037-1606301

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