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.
#226 most reported symptom for this vaccine
Gastrointestinal necrosis has been reported 50 times in association with Rotavirus (Rotateq) vaccination in VAERS. This represents 0.2% of all 25,020 reports for this vaccine.
Among these reports, 7 mentioned death (14.00%) and 49 involved hospitalization (98.0%).
Gastrointestinal necrosis is the #226 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 50 reports of Gastrointestinal necrosis after Rotavirus (Rotateq) vaccination may seem alarming, but context is critical.
The 14.00% 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.