Citizen Petition from Children’s Health Defense

The commenter supports the petition to recall and remove synthetic mRNA COVID-19 vaccines from the market. They argue that the vaccines are causing significant adverse events and deaths, citing data from VAERS as evidence of a safety crisis.

The commenter argues that COVID-19 vaccines are safe, effective, and have saved millions of lives based on extensive peer-reviewed evidence and real-world data. They oppose the petition by stating that revoking vaccine approval would undermine public health and put vulnerable populations at risk.

An epidemiologist argues that COVID-19 vaccines are safe and necessary, specifically refuting claims that they are linked to pediatric deaths. The commenter opposes the petition by highlighting rigorous scientific evidence and surveillance data that show no such link.

The commenter, a lawyer, supports the petition to revoke the licenses of the Comirnaty and Spikevax vaccines. He argues that the vaccines were promoted through fraudulent "bait and switch" tactics, failed to meet Biologics License Application requirements, and caused significant adverse health effects while concealing safety risks from the public.

The commenter supports the action to revoke licenses for the Comirnaty and Spikevax COVID-19 vaccines. They argue that the vaccines were ineffective at stopping transmission, posed significant safety risks as evidenced by VAERS data, and were improperly licensed by the FDA.

The commenter supports the petition to revoke the licenses of the Pfizer-BioNTech and Moderna COVID-19 vaccines. They argue that the vaccines were not properly studied, cite high numbers of adverse events in VAERS, and claim the mRNA platform has shown toxicity and impaired fertility.

An individual is calling for the complete removal of all COVID-19 vaccines from use in children. They argue that the vaccines are dangerous, were inadequately tested, and were administered without proper informed consent.

An anonymous consumer is opposing the expansion of mRNA vaccine authorizations (Comirnaty and Spikevax) due to alleged preclinical data gaps regarding tissue persistence and reproductive toxicity. The commenter demands that the FDA issue an information request, stay the expansion of the biologics, and conduct new longitudinal studies and an independent audit.