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.
3,118 adverse event reports (-1% vs 2015)
In 2016, 3,118 adverse event reports were filed for Tdap (Boostrix) in VAERS. This represents 5.9% of all 52,846 reports for this vaccine.
Of these reports, 4 mentioned death, 101 involved hospitalization, 1,009 required ER visits, and 40 reported disability.
Compared to the average of 2,394 reports per year for this vaccine, 2016 was above average (+30%).
In 2016, reporting for Tdap (Boostrix) was within typical ranges. As always, VAERS data reflects reports filed, not confirmed adverse events. Trends should be interpreted alongside vaccination volume and population health data.
This data comes from the Vaccine Adverse Event Reporting System (VAERS), jointly managed by CDC and FDA.