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.
Pneumococcal (Pneumovax) in 2022
1,080 adverse event reports (-36% vs 2021)
2022 Reporting Summary
In 2022, 1,080 adverse event reports were filed for Pneumococcal (Pneumovax) in VAERS. This represents 1.5% of all 71,157 reports for this vaccine.
Of these reports, 4 mentioned death, 52 involved hospitalization, 145 required ER visits, and 11 reported disability.
Compared to the average of 1,871 reports per year for this vaccine, 2022 was below average (-42%).
💡 What This Means
In 2022, reporting for Pneumococcal (Pneumovax) 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.
All Years for Pneumococcal (Pneumovax)
| Year | Reports | Deaths | Hosp. |
|---|---|---|---|
| 2025 | 252 | 0 | 15 |
| 2024 | 708 | 1 | 23 |
| 2023 | 604 | 1 | 29 |
| 2022 ← current | 1,080 | 4 | 52 |
| 2021 | 1,682 | 9 | 53 |
| 2020 | 3,012 | 4 | 111 |
| 2019 | 3,608 | 10 | 149 |
| 2018 | 4,589 | 11 | 204 |
| 2017 | 5,458 | 7 | 181 |
| 2016 | 6,014 | 10 | 173 |
| 2015 | 3,583 | 10 | 170 |
| 2014 | 3,877 | 21 | 234 |
| 2013 | 3,251 | 12 | 207 |
| 2012 | 3,062 | 6 | 211 |
| 2011 | 2,650 | 3 | 151 |
| 2010 | 3,010 | 11 | 210 |
| 2009 | 2,398 | 16 | 177 |
| 2008 | 2,303 | 11 | 176 |
| 2007 | 2,291 | 6 | 151 |
| 2006 | 1,990 | 8 | 139 |
| 2005 | 1,783 | 4 | 118 |
| 2004 | 1,137 | 5 | 106 |
| 2003 | 1,388 | 12 | 67 |
| 2002 | 1,107 | 7 | 78 |
| 2001 | 1,011 | 8 | 60 |
| 2000 | 917 | 7 | 64 |
| 1999 | 978 | 11 | 69 |
| 1998 | 836 | 6 | 59 |
| 1997 | 616 | 8 | 55 |
| 1996 | 477 | 4 | 41 |
| 1995 | 564 | 6 | 51 |
| 1994 | 345 | 5 | 44 |
| 1993 | 237 | 2 | 33 |
| 1992 | 222 | 5 | 30 |
| 1991 | 215 | 1 | 23 |
| 1990 | 97 | 0 | 8 |
Understanding Yearly Data
Quick Facts
Related Pages
Data Source
This data comes from the Vaccine Adverse Event Reporting System (VAERS), jointly managed by CDC and FDA.