Main highlights of the FDA Meeting:
The FDA Committee approved the Pfizer vaccine Emergency Use Authorization for kids aged 5-11.
Pfizer was asked where is the data that supports the theory that the vaccine will stop transmission in children. Pfizer did not evaluate this as an endpoint in their trial.
Pfizer was also asked how long protection would last, and if boosters would be needed in 6 months for children, similar to what we are seeing in adults. Pfizer "does not have that specific data".
Next, Pfizer was asked about a scenario in their briefing document which showed hospitalizations from vaccine-induced Myocarditis EXCEEDING those from COVID-19.Pfizer acknowledged this is possible, but highlighted that getting children back to school may outweigh this risk.
Both Dr. Jessica Rose and Steve Kirsch are back presenting at the FDA Vaccine Advisory Committee meeting.
Josh Guetzkow, PhD presents at the FDA Vaccine Advisory Committee today.
"Your approval today, means mandates tomorrow for healthy children who don't need it and for those who weren't studied. In the name of millions of parents around the world I implore you - Hold the Line. You won't be able to say you didn't know."
Beatrice Setnik, PhD:
"Long-term complications of Myocarditis after vaccination will not have final reports until May of 2027."
Parent, Amy Alvo, shares the heartbreaking story of her 17-year-old daughter's experience with the Pfizer vaccine and the neurological damage it caused. Her school denied her a medical exemption to avoid a second shot due to Biden's mandates, despite the debilitating neurological damage she suffers through to this day due to this toxic shot.
FDA Committee approved the Pfizer vaccine Emergency Use Authorization for kids aged 5-11 even after they conceded that they didn't know the long-term effects of vaccine on kids.
FDA Voting Member: "We're never gonna learn about how safe the vaccine is until we start giving it."
Dr. Brian Dressen, PhD - Chemist who specializes in developing protections for warfighters and first responders.
"I understand first hand the impact... My wife was severely injured by a single dose of covid vaccine in a clinical trial here in the United States. Because study protocol required 2 doses, she was immediately dropped from the trial and her access to the app (to report her reaction and status) was DELETED. Her reaction was DELIBERATELY LEFT OUT of the final study report."
"My family's life has changed forever. Until we appropriately care for those already injured, acknowledge the full scope of injuries to adults, PLEASE DO NOT GIVE THIS TO KIDS! I do not wish this nightmare on my worst enemy, let alone a child. The suffering of thousands continues to fall on deaf ears at the FDA."
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