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.
Hepatitis B (Engerix-B) in 2017
1,768 adverse event reports (-33% vs 2016)
2017 Reporting Summary
In 2017, 1,768 adverse event reports were filed for Hepatitis B (Engerix-B) in VAERS. This represents 2.4% of all 73,280 reports for this vaccine.
Of these reports, 21 mentioned death, 77 involved hospitalization, 271 required ER visits, and 32 reported disability.
Compared to the average of 1,928 reports per year for this vaccine, 2017 was below average (-8%).
💡 What This Means
In 2017, reporting for Hepatitis B (Engerix-B) 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 Hepatitis B (Engerix-B)
| Year | Reports | Deaths | Hosp. |
|---|---|---|---|
| 2025 | 1,712 | 3 | 27 |
| 2024 | 1,912 | 9 | 24 |
| 2023 | 1,857 | 5 | 24 |
| 2022 | 1,623 | 7 | 29 |
| 2021 | 1,405 | 13 | 31 |
| 2020 | 925 | 7 | 31 |
| 2019 | 1,248 | 21 | 74 |
| 2018 | 1,120 | 12 | 48 |
| 2017 ← current | 1,768 | 21 | 77 |
| 2016 | 2,639 | 11 | 70 |
| 2015 | 2,243 | 15 | 63 |
| 2014 | 1,534 | 6 | 75 |
| 2013 | 1,250 | 16 | 64 |
| 2012 | 1,578 | 23 | 99 |
| 2011 | 1,308 | 32 | 144 |
| 2010 | 1,426 | 25 | 126 |
| 2009 | 1,486 | 30 | 150 |
| 2008 | 1,539 | 16 | 130 |
| 2007 | 1,290 | 13 | 111 |
| 2006 | 1,118 | 18 | 86 |
| 2005 | 1,166 | 25 | 92 |
| 2004 | 1,403 | 51 | 86 |
| 2003 | 1,658 | 63 | 136 |
| 2002 | 2,092 | 48 | 141 |
| 2001 | 2,105 | 58 | 188 |
| 2000 | 2,384 | 47 | 199 |
| 1999 | 2,497 | 66 | 265 |
| 1998 | 2,570 | 56 | 202 |
| 1997 | 2,805 | 65 | 230 |
| 1996 | 2,842 | 58 | 249 |
| 1995 | 2,992 | 71 | 323 |
| 1994 | 3,456 | 88 | 336 |
| 1993 | 3,858 | 94 | 254 |
| 1992 | 3,567 | 18 | 193 |
| 1991 | 2,584 | 4 | 105 |
| 1990 | 459 | 2 | 35 |
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.