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.
#240 most reported symptom for this vaccine
Cyanosis has been reported 110 times in association with Influenza, Seasonal (Flulaval Quadrivalent) vaccination in VAERS. This represents 0.2% of all 52,111 reports for this vaccine.
Among these reports, 6 mentioned death (5.45%) and 12 involved hospitalization (10.9%).
Cyanosis is the #240 most frequently reported symptom for Influenza, Seasonal (Flulaval Quadrivalent) out of 2354 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 110 reports of Cyanosis after Influenza, Seasonal (Flulaval Quadrivalent) vaccination may seem alarming, but context is critical.
The 5.45% 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.