🇺🇸 INTERFERON GAMMA-1A in United States

20 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. Abdominal Distension — 2 reports (10%)
  2. Abdominal Pain — 2 reports (10%)
  3. Clostridium Difficile Colitis — 2 reports (10%)
  4. Dehydration — 2 reports (10%)
  5. Diarrhoea — 2 reports (10%)
  6. Hypotension — 2 reports (10%)
  7. Nausea — 2 reports (10%)
  8. Pseudomembranous Colitis — 2 reports (10%)
  9. Pyrexia — 2 reports (10%)
  10. Tachycardia — 2 reports (10%)

Source database →

INTERFERON GAMMA-1A 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 INTERFERON GAMMA-1A approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for INTERFERON GAMMA-1A in United States?

Marketing authorisation holder not available in our data.