🇺🇸 tegafur-uracil in United States
149 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: 149
Most-reported reactions
- Diarrhoea — 38 reports (25.5%)
- Neutropenia — 18 reports (12.08%)
- Anaemia — 14 reports (9.4%)
- Vomiting — 14 reports (9.4%)
- Decreased Appetite — 11 reports (7.38%)
- Dehydration — 11 reports (7.38%)
- Pyrexia — 11 reports (7.38%)
- Stomatitis — 11 reports (7.38%)
- Thrombocytopenia — 11 reports (7.38%)
- Leukopenia — 10 reports (6.71%)
Other Oncology approved in United States
Frequently asked questions
Is tegafur-uracil approved in United States?
tegafur-uracil does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for tegafur-uracil in United States?
Yokohama City University is the originator. The local marketing authorisation holder may differ — check the official source linked above.