🇺🇸 LUTROPIN ALFA in United States

239 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. Ovarian Hyperstimulation Syndrome — 106 reports (44.35%)
  2. Abdominal Pain — 28 reports (11.72%)
  3. Abdominal Distension — 26 reports (10.88%)
  4. Dyspnoea — 20 reports (8.37%)
  5. Chest Discomfort — 12 reports (5.02%)
  6. Ascites — 10 reports (4.18%)
  7. Nausea — 10 reports (4.18%)
  8. Tension — 10 reports (4.18%)
  9. Ovarian Haemorrhage — 9 reports (3.77%)
  10. Asthenia — 8 reports (3.35%)

Source database →

LUTROPIN ALFA 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 LUTROPIN ALFA approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for LUTROPIN ALFA in United States?

Marketing authorisation holder not available in our data.