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.
#40 most reported symptom for this vaccine
Inappropriate schedule of product administration has been reported 2,196 times in association with Zoster Live (Zostavax) vaccination in VAERS. This represents 1.6% of all 140,312 reports for this vaccine.
Among these reports, 0 mentioned death (0.00%) and 33 involved hospitalization (1.5%).
Inappropriate schedule of product administration is the #40 most frequently reported symptom for Zoster Live (Zostavax) out of 2827 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 2,196 reports of Inappropriate schedule of product administration after Zoster Live (Zostavax) vaccination may seem alarming, but context is critical. With 140,312 total reports for this vaccine (representing many millions of doses), Inappropriate schedule of product administration appears in only 1.6% of reports.
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.