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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.

COVID-19 Vaccine2022

COVID-19 Vaccine in 2022

221,580 adverse event reports (-71% vs 2021)

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221,580
Reports
8,133
Deaths
38,360
Hospitalizations
26,332
ER Visits
6,043
Disabilities

2022 Reporting Summary

In 2022, 221,580 adverse event reports were filed for COVID-19 Vaccine in VAERS. This represents 19.8% of all 1,121,388 reports for this vaccine.

Of these reports, 8,133 mentioned death, 38,360 involved hospitalization, 26,332 required ER visits, and 6,043 reported disability.

Compared to the average of 153,760 reports per year for this vaccine, 2022 was above average (+44%).

💡 What This Means

High report volume: 221,580 reports in a single year is significant. This typically reflects large-scale vaccination campaigns rather than increased risk per dose. Without knowing total doses administered in 2022, raw report counts cannot indicate safety rates.

Death reports require context: 8,133 death reports does not mean the vaccine caused 8,133 deaths. VAERS accepts all reports regardless of causation. Many recipients are elderly or have comorbidities, and background mortality rates must be considered.

All Years for COVID-19 Vaccine

YearReportsDeathsHosp.
20265002072
202510,6445401,211
202420,2468242,117
202354,7202,08713,999
2022 ← current221,5808,13338,360
2021757,74712,95558,027
202010,88316155

Understanding Yearly Data

Spikes may reflect awareness: Years with unusual activity (e.g., pandemic) often see increased reporting.
Dose volume matters: More vaccinations given in a year naturally leads to more reports.
Reporting lag: Some events are reported months after they occur, so recent years may be incomplete.

Quick Facts

Reports:221,580
Deaths:8,133
Hospitalizations:38,360
% of Total:19.8%
Rank (by vol.):#2 of 7 years
Avg/year:153,760

Data Source

This data comes from the Vaccine Adverse Event Reporting System (VAERS), jointly managed by CDC and FDA.