🇺🇸 Thienopyridine in United States
27 US adverse-event reports
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: 28 March 2025 – 28 March 2026
- Total reports: 27
Most-reported reactions
- Acute Myocardial Infarction — 5 reports (18.52%)
- Blood Creatinine Increased — 3 reports (11.11%)
- Dyspnoea — 3 reports (11.11%)
- Haemorrhage — 3 reports (11.11%)
- Post Procedural Complication — 3 reports (11.11%)
- Angina Pectoris — 2 reports (7.41%)
- Blood Pressure Increased — 2 reports (7.41%)
- Blood Pressure Systolic Increased — 2 reports (7.41%)
- Colon Cancer — 2 reports (7.41%)
- Electrocardiogram St Segment Elevation — 2 reports (7.41%)
Other Other approved in United States
Frequently asked questions
Is Thienopyridine approved in United States?
Thienopyridine does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Thienopyridine in United States?
Boston Scientific Corporation is the originator. The local marketing authorisation holder may differ — check the official source linked above.