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.
#402 most reported symptom for this vaccine
Transfusion has been reported 21 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 (4.76%) and 19 involved hospitalization (90.5%).
Transfusion is the #402 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 21 reports of Transfusion after Rotavirus (Rotateq) vaccination may seem alarming, but context is critical.
The mortality rate of 4.76% 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.