🇺🇸 Influenza Virus Vaccine Inactivated in United States

30 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. Cough — 4 reports (13.33%)
  2. Fatigue — 4 reports (13.33%)
  3. Malaise — 4 reports (13.33%)
  4. Arthralgia — 3 reports (10%)
  5. Nausea — 3 reports (10%)
  6. Oropharyngeal Pain — 3 reports (10%)
  7. Pain In Extremity — 3 reports (10%)
  8. Acute Kidney Injury — 2 reports (6.67%)
  9. Asthenia — 2 reports (6.67%)
  10. Blood Thyroid Stimulating Hormone Increased — 2 reports (6.67%)

Source database →

Influenza Virus Vaccine Inactivated 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 Influenza Virus Vaccine Inactivated approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for Influenza Virus Vaccine Inactivated in United States?

National Institute of Allergy and Infectious Diseases (NIAID) is the originator. The local marketing authorisation holder may differ — check the official source linked above.