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Frontline Doctors Call FDA Approval of Pfizer Vaccine Grossly Negligent

America’s Frontline Doctors Points to Pfizer’s Ending Blind Trials and Violating Federal Regulations That Require Open Forums, Greater Transparency LOS ANGELES, CA – America’s Frontline Doctors released the following statement today in response to the FDA’s approval of the Pfizer COVID-19 vaccine: “AFLDS decries the FDA’s unprecedented and grossly negligent approval of the Pfizer Covid vaccine, years before completion of their phase three trials. The vaccine was authorized for a variant of the virus that has faded from circulation. The current vaccine is known to be an ineffective and “leaky” vaccine (defined as a vaccine that produces stronger variants once in circulation) against the current variant. “Vaccine efficacy versus the current Delta strain is inferior to safe, effective treatments the doctors of ALFDS are recommending and would never have qualified for Emergency Use Authorization. “Pfizer unblinded their trial after a few months and gave the product to all, eliminating the placebo arm, making this trial all but useless. “The vaccine panelists within FDA have numerous financial and other conflicts of interest, and the FDA itself receives industry funding. For example, recent FDA Commissioner Hahn just accepted a job with the financiers of Moderna. This decision also violates the Federal Advisory Committee Act (FACA) that requires open forums. “This exposes the FDA as a rubber stamp for Big Pharma and the Biden administration. AFLDS is considering filing for a Temporary Restraining Order lawsuit based on the FACA violation.”

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