🇺🇸 Fluoxetine 20 MG in United States

26 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. Product Substitution Issue — 4 reports (15.38%)
  2. Rash — 4 reports (15.38%)
  3. Drug Ineffective — 3 reports (11.54%)
  4. Headache — 3 reports (11.54%)
  5. Abdominal Pain — 2 reports (7.69%)
  6. Abnormal Behaviour — 2 reports (7.69%)
  7. Anxiety — 2 reports (7.69%)
  8. Chest Discomfort — 2 reports (7.69%)
  9. Confusional State — 2 reports (7.69%)
  10. Cough — 2 reports (7.69%)

Source database →

Fluoxetine 20 MG 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 Fluoxetine 20 MG approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for Fluoxetine 20 MG in United States?

Wake Forest University Health Sciences is the originator. The local marketing authorisation holder may differ — check the official source linked above.