May 22, 2023: The FDA and Pfizer cannot claim ignorance when it comes to placing American civilians at unnecessary risk for injury, harm, and death, especially when it comes to children. The injection of children with mRNA technology was never merited because the risk of children contracting COVID-19 was insignificant per the FDA’s own documents.
The truly damning evidence is from a 2020 document, when Pfizer ordered the FDA to cover-up the harmful effects the mRNA injections had on children and not disclose these findings to the public.
On June 10, 2021, the FDA met to discuss the clinical endpoints for children’s COVID-19 vaccine studies. Per the FDA briefing document, the committee stated that conducting a pediatric trial where the primary endpoint is reduction in risk for COVID-19 infection in vaccinated children versus unvaccinated children would be impossible (infeasible) to conduct,because children rarely become infected.9
Pfizer knowingly violated safety laws andplaced children at unnecessary risk for injury, harm, and death per their November 20, 2020, FDA Phase 3 data submission.3 Pfizer’s report states that there was data from 100 children aged 12 to 15 years, who experienced reactogenicity effects from the mRNA injections (i.e. myocarditis, seizures, blood clots, death, etc.). However, the Sponsor (Pfizer/BioNTech) requested that thedata for these 100 childrenNOT be disclosedbecause the benefit-risk ratio was unfavorable.
Verbatim from pages 15-16 of Pfizer’s Phase-3 FDA document…