Comment from GOMEZ, VIRGINIA
AnonymousSupportIndividual
Summary: The commenter is an individual demanding that the FDA revoke the licenses for the Comirnaty and Spikevax COVID-19 vaccines. They argue that the manufacturers failed to meet Biologics License Application requirements and cite high numbers of reported adverse events as evidence of the vaccines' danger.
I DEMAND the revokation of all licenses for Comirnaty and Spikevax COVID vaccines for all demographic groups because the manufacturers never met the requirements for a Biologics License Application as established by the FDA. The impacts upon the health of our nation’s citizens and the state of personal freedom in our country by these improperly licensed vaccines have been catastrophic. An estimated 32 people (in 1976) died following vaccination for the swine flu, prompting the immediate end to the swine flu vaccine campaign in the U.S. In contrast, from December 2020 through November 28, 2025, there have been 1,671,991 adverse events reported to the Vaccine Adverse Events Reporting System for the COVID-19 vaccines, including 38,913 deaths. Yet these products have remained on the market, heavily endorsed, promoted, and often mandated for people of all ages including young children.
Therefore I urge you to revoke the improperly-granted licenses for these extremely dangerous vaccines.