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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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| Publicado no: | TH Open |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Georg Thieme Verlag KG
2017
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6524845/ https://ncbi.nlm.nih.gov/pubmed/31249915 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0037-1606301 |
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