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.
Tdap (Boostrix) has 52,846 reports in VAERS spanning from 1990 to 2026. Of these reports, 129 mentioned death, 2,191 involved hospitalization, and 14,141 required emergency department visits. This vaccine is manufactured by: Sanofi Pasteur, GlaxoSmithKline, Unknown Manufacturer. This vaccine accounts for 2.7% of all 1,983,260 reports in the VAERS database.
Tdap (Boostrix) has 52,846 reports in VAERS spanning from 1990 to 2026.
Of these reports, 129 mentioned death, 2,191 involved hospitalization, and 14,141 required emergency department visits.
This vaccine is manufactured by: Sanofi Pasteur, GlaxoSmithKline, Unknown Manufacturer.
This vaccine accounts for 2.7% of all 1,983,260 reports in the VAERS database.
This vaccine averages 2,402 reports per year over 22 years of reporting (2005–2026).
This data comes from the Vaccine Adverse Event Reporting System (VAERS), jointly managed by CDC and FDA.