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.
#1579 most reported symptom for this vaccine
Ophthalmological examination abnormal has been reported 5 times in association with Tdap (Boostrix) vaccination in VAERS. This represents 0.0% of all 52,846 reports for this vaccine.
Among these reports, 1 mentioned death (20.00%) and 1 involved hospitalization (20.0%).
Ophthalmological examination abnormal is the #1579 most frequently reported symptom for Tdap (Boostrix) out of 2243 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 5 reports of Ophthalmological examination abnormal after Tdap (Boostrix) vaccination may seem alarming, but context is critical.
The 20.00% 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.