🇺🇸 Pred Forte in United States

1,688 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. Eye Pain — 312 reports (18.48%)
  2. Off Label Use — 196 reports (11.61%)
  3. Drug Ineffective — 192 reports (11.37%)
  4. Vision Blurred — 182 reports (10.78%)
  5. Eye Irritation — 156 reports (9.24%)
  6. Headache — 150 reports (8.89%)
  7. Ocular Hyperaemia — 140 reports (8.29%)
  8. Fatigue — 129 reports (7.64%)
  9. Cataract — 121 reports (7.17%)
  10. Nausea — 110 reports (6.52%)

Source database →

Pred Forte 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 Pred Forte approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for Pred Forte in United States?

University of Colorado, Denver is the originator. The local marketing authorisation holder may differ — check the official source linked above.