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 2017
5,458 adverse event reports (-9% vs 2016)
2017 Reporting Summary
In 2017, 5,458 adverse event reports were filed for Pneumococcal (Pneumovax) in VAERS. This represents 7.7% of all 71,157 reports for this vaccine.
Of these reports, 7 mentioned death, 181 involved hospitalization, 1,042 required ER visits, and 49 reported disability.
Compared to the average of 1,871 reports per year for this vaccine, 2017 was above average (+192%).
💡 What This Means
In 2017, 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 | 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 ← current | 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.