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.
#384 most reported symptom for this vaccine
Incorrect route of product administration has been reported 42 times in association with Pneumococcal (Prevnar13) vaccination in VAERS. This represents 0.1% of all 33,058 reports for this vaccine.
Among these reports, 1 mentioned death (2.38%) and 0 involved hospitalization (0.0%).
Incorrect route of product administration is the #384 most frequently reported symptom for Pneumococcal (Prevnar13) out of 1920 total symptoms.
Disclaimer: VAERS reports describe events that occurred after vaccination but do not establish that the vaccine caused the event. Many reported symptoms may be coincidental or related to underlying conditions.
Seeing 42 reports of Incorrect route of product administration after Pneumococcal (Prevnar13) vaccination may seem alarming, but context is critical.
The mortality rate of 2.38% warrants monitoring, though VAERS deaths represent temporal associations, not confirmed causal links.
This data comes from the Vaccine Adverse Event Reporting System (VAERS), jointly managed by CDC and FDA.