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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.
Red blood cell sedimentation rate increased
3,463 total reports40.1% serious outcomes
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3,463
Total Reports
36
Deaths
1,352
Hospitalizations
40.1
Severity Rate
% serious outcomes
About Red blood cell sedimentation rate increased Reports
Red blood cell sedimentation rate increased has been reported 3,463 times in VAERS from 1990 to 2026.
Of these reports, 36 were associated with death (1.04%) and 1,352 involved hospitalization.
The overall serious outcome rate (death or hospitalization) for reports mentioning Red blood cell sedimentation rate increased is 40.1%.
Understanding Red blood cell sedimentation rate increased in VAERS
•Temporal association only: These reports show Red blood cell sedimentation rate increased 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 Red blood cell sedimentation rate increased. 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. COVID192,080
2. FLU3398
3. HEP333
4. MMR242
5. PPV230
6. SMALL225
7. HPV4183
8. ANTH182
9. FLUX176
10. VARZOS151
Quick Facts
Reports:3,463
Deaths:36
Hospitalizations:1,352
Mortality Rate:1.04%
Severity Rate:40.1%
Related Analysis
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Data Source
This data comes from the Vaccine Adverse Event Reporting System (VAERS), jointly managed by CDC and FDA.