Drug Landscape ›
Enteric Coated Aspirin ›
Regulatory · United States
Marketing authorisation
FDA
Safety signals — FAERS
Adverse reaction reports describe suspected side effects. A report does not mean the drug caused the event — co-medications, underlying disease and coincidence all contribute.
Window: 20 April 2025 – 20 April 2026
Total reports: 252
Most-reported reactions
Myocardial Infarction — 79 reports (31.35%) Coronary Artery Disease — 46 reports (18.25%) Cardiac Failure Congestive — 39 reports (15.48%) Acute Myocardial Infarction — 28 reports (11.11%) Cerebrovascular Accident — 14 reports (5.56%) Fall — 10 reports (3.97%) Arthrofibrosis — 9 reports (3.57%) Atrial Fibrillation — 9 reports (3.57%) Dyspnoea — 9 reports (3.57%) Nausea — 9 reports (3.57%)
Source database →
Enteric Coated Aspirin in other countries
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Frequently asked questions
Is Enteric Coated Aspirin approved in United States?
Yes. FDA has authorised it.
Who is the marketing authorisation holder for Enteric Coated Aspirin in United States?
Dartmouth-Hitchcock Medical Center is the originator. The local marketing authorisation holder may differ — check the official source linked above.