Important: VAERS reports alone cannot determine if a vaccine caused an adverse event. Reports may contain incomplete, inaccurate, or unverified information. Correlation does not equal causation.
Influenza, Seasonal (Fluvirin) has 119,695 reports in VAERS spanning from 1990 to 2026. Of these reports, 1,081 mentioned death, 8,325 involved hospitalization, and 37,032 required emergency department visits. This vaccine is manufactured by: Sanofi Pasteur, Novartis, GlaxoSmithKline, CSL Limited, Connaught Laboratories, Pfizer / Wyeth, Seqirus, Evans Vaccines, Parke-davis, Medeva Pharma, Ltd., Aventis Pasteur, Parkdale Pharmaceuticals, Lederle Laboratories. This vaccine accounts for 6.0% of all 1,983,260 reports in the VAERS database.
Influenza, Seasonal (Fluvirin) has 119,695 reports in VAERS spanning from 1990 to 2026.
Of these reports, 1,081 mentioned death, 8,325 involved hospitalization, and 37,032 required emergency department visits.
This vaccine is manufactured by: Sanofi Pasteur, Novartis, GlaxoSmithKline, CSL Limited, Connaught Laboratories, Pfizer / Wyeth, Seqirus, Evans Vaccines, Parke-davis, Medeva Pharma, Ltd., Aventis Pasteur, Parkdale Pharmaceuticals, Lederle Laboratories.
This vaccine accounts for 6.0% of all 1,983,260 reports in the VAERS database.
This vaccine averages 3,235 reports per year over 37 years of reporting (1990–2026).
This data comes from the Vaccine Adverse Event Reporting System (VAERS), jointly managed by CDC and FDA.