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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.
Incorrect route of product administration
4,172 total reports1.1% serious outcomes
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4,172
Total Reports
4
Deaths
40
Hospitalizations
1.1
Severity Rate
% serious outcomes
About Incorrect route of product administration Reports
Incorrect route of product administration has been reported 4,172 times in VAERS from 1990 to 2026.
Of these reports, 4 were associated with death (0.10%) and 40 involved hospitalization.
The overall serious outcome rate (death or hospitalization) for reports mentioning Incorrect route of product administration is 1.1%.
Understanding Incorrect route of product administration in VAERS
•Temporal association only: These reports show Incorrect route of product administration 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 Incorrect route of product administration. 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. COVID191,590
2. MMR537
3. VARZOS534
4. SMALLMNK337
5. VARCEL283
6. FLU4233
7. TDAP156
8. UNK142
9. MMRV136
10. YF96
Quick Facts
Reports:4,172
Deaths:4
Hospitalizations:40
Mortality Rate:0.10%
Severity Rate:1.1%
Related Analysis
Explore Further
Data Source
This data comes from the Vaccine Adverse Event Reporting System (VAERS), jointly managed by CDC and FDA.