🇺🇸 Coumarin/troxerutin in United States
39 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: 22 April 2025 – 22 April 2026
- Total reports: 39
Most-reported reactions
- Fatigue — 5 reports (12.82%)
- Malaise — 5 reports (12.82%)
- Vomiting — 5 reports (12.82%)
- Abdominal Pain — 4 reports (10.26%)
- Pain — 4 reports (10.26%)
- Pain In Extremity — 4 reports (10.26%)
- Blood Pressure Increased — 3 reports (7.69%)
- Cardiovascular Disorder — 3 reports (7.69%)
- Diarrhoea — 3 reports (7.69%)
- Drug Ineffective — 3 reports (7.69%)
Other Cardiovascular / Vascular approved in United States
Frequently asked questions
Is Coumarin/troxerutin approved in United States?
Coumarin/troxerutin does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Coumarin/troxerutin in United States?
Takeda is the originator. The local marketing authorisation holder may differ — check the official source linked above.