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.
#487 most reported symptom for this vaccine
Incorrect route of product administration has been reported 16 times in association with Rotavirus (Rotateq) vaccination in VAERS. This represents 0.1% of all 25,020 reports for this vaccine.
Among these reports, 1 mentioned death (6.25%) and 0 involved hospitalization (0.0%).
Incorrect route of product administration is the #487 most frequently reported symptom for Rotavirus (Rotateq) out of 1365 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 16 reports of Incorrect route of product administration after Rotavirus (Rotateq) vaccination may seem alarming, but context is critical.
The 6.25% mortality rate among these reports is elevated, but this reflects the severity of the condition itself rather than vaccine causation.
This data comes from the Vaccine Adverse Event Reporting System (VAERS), jointly managed by CDC and FDA.