A Pharmacovigilance Study of Adverse Drug Reactions Reported for Cardiovascular Disease Medications Approved Between 2012 and 2017 in the United States Food and Drug Administration Adverse Event Reporting System (FAERS) Database
Niti M. Patel, Britney A. Stottlemyer, Matthew P. Gray, Richard D. Boyce, Sandra L. Kane‐Gill
Topics & Concepts
MedicineAdverse Event Reporting SystemPharmacovigilanceAdverse effectPostmarketing surveillanceMedDRADabigatranInternal medicineFebuxostatIntensive care medicineWarfarinAtrial fibrillationHyperuricemiaUric acidPharmacovigilance and Adverse Drug ReactionsAtrial Fibrillation Management and OutcomesCardiac electrophysiology and arrhythmias