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This spontaneous report received from a consumer
The batch number was not reported.
It was unknown that whether autopsy performed for reported patients.
The event(s) has an unknown/unclear temporal relationship, is unlabeled, and has unknown scientific plausibility.
originally posted by: Phage
a reply to: TritonTaranis
The truth is they’re higher than all other combined vaccine VEARS since forever
With which other vaccines is it required that adverse events be reported?
What to Report After Any Vaccination
Healthcare providers are required by law to report to VAERS:
• Any adverse event listed in the VAERS Table of Reportable Events Following Vaccination that occurs within the specified time period after vaccination
• Any adverse event listed by the vaccine manufacturer as a contraindication to further doses of the vaccine
Effective date: March 21, 2017. The Reportable Events Table (RET) reflects what is reportable by law (42 USC 300aa-25)