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.
995 adverse event reports (-10% vs 2021)
In 2022, 995 adverse event reports were filed for Pneumococcal (Prevnar13) in VAERS. This represents 3.0% of all 33,058 reports for this vaccine.
Of these reports, 18 mentioned death, 65 involved hospitalization, 129 required ER visits, and 14 reported disability.
Compared to the average of 1,960 reports per year for this vaccine, 2022 was below average (-49%).
In 2022, reporting for Pneumococcal (Prevnar13) 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.