🇺🇸 URIDINE TRIACETATE in United States

34 US adverse-event reports

Marketing authorisation

FDA

  • Status: approved

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.

Most-reported reactions

  1. Off Label Use — 5 reports (14.71%)
  2. Mucosal Inflammation — 4 reports (11.76%)
  3. Thrombocytopenia — 4 reports (11.76%)
  4. Diarrhoea — 3 reports (8.82%)
  5. Drug Ineffective For Unapproved Indication — 3 reports (8.82%)
  6. Dysphagia — 3 reports (8.82%)
  7. Gastroenteritis — 3 reports (8.82%)
  8. Neutropenic Colitis — 3 reports (8.82%)
  9. Stomatitis — 3 reports (8.82%)
  10. Toxicity To Various Agents — 3 reports (8.82%)

Source database →

URIDINE TRIACETATE 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 URIDINE TRIACETATE approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for URIDINE TRIACETATE in United States?

Marketing authorisation holder not available in our data.