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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.
Vaccine positive rechallenge
4,759 total reports3.4% serious outcomes
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4,759
Total Reports
5
Deaths
158
Hospitalizations
3.4
Severity Rate
% serious outcomes
About Vaccine positive rechallenge Reports
Vaccine positive rechallenge has been reported 4,759 times in VAERS from 1990 to 2026.
Of these reports, 5 were associated with death (0.11%) and 158 involved hospitalization.
The overall serious outcome rate (death or hospitalization) for reports mentioning Vaccine positive rechallenge is 3.4%.
Understanding Vaccine positive rechallenge in VAERS
•Temporal association only: These reports show Vaccine positive rechallenge occurred after vaccination, not necessarily because of vaccination.
•Background rates matter: Many symptoms occur naturally at baseline rates in the population, unrelated to vaccination.
•Reporting variability: Medical terminology may be used differently by various healthcare providers and over time.
•Investigation needed: High-frequency reports may trigger further epidemiological studies to determine causation.
What This Data Shows
Most Associated Vaccines: The vaccines most frequently mentioned in reports with Vaccine positive rechallenge. This may reflect usage patterns, not causation.
Severity Patterns: The percentage of reports that involve serious outcomes can help prioritize safety investigations.
Reporting Trends: Changes in reporting frequency over time may reflect increased awareness, media attention, or actual safety signals.
Most Associated Vaccines
1. COVID192,552
2. VARZOS959
3. HPV4782
4. FLU3230
5. PNC226
6. FLUX168
7. HIBV152
8. ANTH143
9. HEP141
10. DTAP127
Quick Facts
Reports:4,759
Deaths:5
Hospitalizations:158
Mortality Rate:0.11%
Severity Rate:3.4%
Related Analysis
Explore Further
Data Source
This data comes from the Vaccine Adverse Event Reporting System (VAERS), jointly managed by CDC and FDA.