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.
#218 most reported symptom for this vaccine
Wrong technique in product usage process has been reported 11 times in association with Influenza, Seasonal (Fluad Quadrivalent) vaccination in VAERS. This represents 0.3% of all 4,184 reports for this vaccine.
Among these reports, 0 mentioned death (0.00%) and 0 involved hospitalization (0.0%).
Wrong technique in product usage process is the #218 most frequently reported symptom for Influenza, Seasonal (Fluad Quadrivalent) out of 673 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 11 reports of Wrong technique in product usage process after Influenza, Seasonal (Fluad Quadrivalent) 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.