🇺🇸 Fluarix Quadrivalent in United States

138 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. Anxiety — 17 reports (12.32%)
  2. Malaise — 17 reports (12.32%)
  3. Fatigue — 15 reports (10.87%)
  4. Pain — 15 reports (10.87%)
  5. Dyspnoea — 13 reports (9.42%)
  6. Influenza — 13 reports (9.42%)
  7. Back Pain — 12 reports (8.7%)
  8. Cough — 12 reports (8.7%)
  9. Diarrhoea — 12 reports (8.7%)
  10. Urinary Tract Infection — 12 reports (8.7%)

Source database →

Fluarix Quadrivalent 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 Fluarix Quadrivalent approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for Fluarix Quadrivalent in United States?

ModernaTX, Inc. is the originator. The local marketing authorisation holder may differ — check the official source linked above.