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.
#117 most reported symptom for this vaccine
Haemoglobin decreased has been reported 107 times in association with Rotavirus (Rotateq) vaccination in VAERS. This represents 0.4% of all 25,020 reports for this vaccine.
Among these reports, 6 mentioned death (5.61%) and 89 involved hospitalization (83.2%).
Haemoglobin decreased is the #117 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 107 reports of Haemoglobin decreased after Rotavirus (Rotateq) vaccination may seem alarming, but context is critical.
The 5.61% 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.