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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 product formulation administered

9,496 total reports0.2% serious outcomes

9,496

Total Reports

Deaths

Hospitalizations

0.2

Severity Rate

% serious outcomes

About Incorrect product formulation administered Reports

Incorrect product formulation administered has been reported 9,496 times in VAERS from 1990 to 2026.

Of these reports, 8 were associated with death (0.08%) and 7 involved hospitalization.

The overall serious outcome rate (death or hospitalization) for reports mentioning Incorrect product formulation administered is 0.2%.

Understanding Incorrect product formulation administered in VAERS

•Temporal association only: These reports show Incorrect product formulation administered 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 product formulation administered. 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.