🇺🇸 Fluarix Tetra in United States

22 US adverse-event reports

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.

• Window: 23 April 2025 – 23 April 2026
• Total reports: 22

Most-reported reactions

1. Anaphylactic Reaction — 3 reports (13.64%)
2. Covid-19 — 3 reports (13.64%)
3. Abdominal Distension — 2 reports (9.09%)
4. Abdominal Pain — 2 reports (9.09%)
5. Anogenital Warts — 2 reports (9.09%)
6. Dyspnoea — 2 reports (9.09%)
7. Exposure During Pregnancy — 2 reports (9.09%)
8. Hypertension — 2 reports (9.09%)
9. Hypotension — 2 reports (9.09%)
10. Influenza — 2 reports (9.09%)

Source database →

Frequently asked questions

Is Fluarix Tetra approved in United States?

Fluarix Tetra does not currently have US marketing authorisation in our dataset.

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

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