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.
#3 most reported symptom for this vaccine
Incorrect route of product administration has been reported 337 times in association with Smallpox + Monkeypox (Jynneos) vaccination in VAERS. This represents 14.7% of all 2,292 reports for this vaccine.
Among these reports, 0 mentioned death (0.00%) and 1 involved hospitalization (0.3%).
Incorrect route of product administration is the #3 most frequently reported symptom for Smallpox + Monkeypox (Jynneos) out of 283 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 337 reports of Incorrect route of product administration after Smallpox + Monkeypox (Jynneos) 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.