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.
3,039 adverse event reports (+259% vs 2000)
In 2001, 3,039 adverse event reports were filed for Pneumococcal (Prevnar) in VAERS. This represents 10.9% of all 27,970 reports for this vaccine.
Of these reports, 88 mentioned death, 360 involved hospitalization, 1,330 required ER visits, and 15 reported disability.
Compared to the average of 1,188 reports per year for this vaccine, 2001 was above average (+156%).
Year-over-year change: The large change from 2000 likely reflects a ramp-up in vaccination (e.g., new vaccine rollout or expanded eligibility) rather than a change in per-dose risk.
This data comes from the Vaccine Adverse Event Reporting System (VAERS), jointly managed by CDC and FDA.