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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.
Nuclear magnetic resonance imaging
3,532 total reports42.0% serious outcomes
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3,532
Total Reports
36
Deaths
1,447
Hospitalizations
42
Severity Rate
% serious outcomes
About Nuclear magnetic resonance imaging Reports
Nuclear magnetic resonance imaging has been reported 3,532 times in VAERS from 1990 to 2026.
Of these reports, 36 were associated with death (1.02%) and 1,447 involved hospitalization.
The overall serious outcome rate (death or hospitalization) for reports mentioning Nuclear magnetic resonance imaging is 42.0%.
Understanding Nuclear magnetic resonance imaging in VAERS
•Temporal association only: These reports show Nuclear magnetic resonance imaging 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 Nuclear magnetic resonance imaging. 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. FLU31,170
2. HPV4865
3. VARZOS503
4. TDAP403
5. FLUX375
6. MNQ293
7. FLU4261
8. HEPA247
9. PPV220
10. PNC13216
Quick Facts
Reports:3,532
Deaths:36
Hospitalizations:1,447
Mortality Rate:1.02%
Severity Rate:42.0%
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.