🇺🇸 TRIFAROTENE in United States

56 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. Urinary Retention — 15 reports (26.79%)
  2. Mydriasis — 13 reports (23.21%)
  3. Vision Blurred — 8 reports (14.29%)
  4. Drug Interaction — 6 reports (10.71%)
  5. Toxicity To Various Agents — 4 reports (7.14%)
  6. Abdominal Distension — 2 reports (3.57%)
  7. Adnexal Torsion — 2 reports (3.57%)
  8. Dysuria — 2 reports (3.57%)
  9. Liver Injury — 2 reports (3.57%)
  10. Micturition Urgency — 2 reports (3.57%)

Source database →

TRIFAROTENE 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 TRIFAROTENE approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for TRIFAROTENE in United States?

Marketing authorisation holder not available in our data.