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.
#320 most reported symptom for this vaccine
Respiratory syncytial virus infection has been reported 29 times in association with Rotavirus (Rotateq) vaccination in VAERS. This represents 0.1% of all 25,020 reports for this vaccine.
Among these reports, 0 mentioned death (0.00%) and 22 involved hospitalization (75.9%).
Respiratory syncytial virus infection is the #320 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 29 reports of Respiratory syncytial virus infection after Rotavirus (Rotateq) vaccination may seem alarming, but context is critical.
The mortality rate among these reports is very low at 0.00%, suggesting most cases are non-fatal.
This data comes from the Vaccine Adverse Event Reporting System (VAERS), jointly managed by CDC and FDA.