BREAKING: Despite thousands of deaths and adverse reactions FDA rushes to grant full approval to Pfizer COVID jab

(Lifesite News, Aug 23, 2021)

WASHINGTON, D.C. (LifeSiteNews) – The U.S. Food and Drug Administration (FDA) has given its full approval to the abortion-tainted Pfizer/BioNTech COVID-19 vaccine, despite thousands of deaths and other serious adverse reactions being recorded by individuals who have received the jab.

The full permission, described by the agency as a “key achievement for public health,” comes despite the National Institutes for Health (NIH) estimating a trial completion date for testing the efficacy and safety of the jab to be around May 2, 2023, for the Pfizer shot.

The FDA had originally granted the mRNA jab emergency use authorization (EUA) in December, 2020, becoming the second “vaccine” technology of its kind to be permitted for emergency use in the U.S., after Moderna’s mRNA shot.

Now, the FDA has given its full approval to the jab, which has been renamed “Comirnaty” for marketing purposes, to individuals aged 16 and older. For those between 12 and 15 years of age, the EUA still applies. The FDA noted that “the administration of a third dose in certain immunocompromised individuals” will also still only be granted under the EUA protocol.

The FDA’s Acting Commissioner, Janet Woodcock, called the full authorization a “milestone” in the “battle” against COVID-19, and said that the jab had met “rigorous, scientific standards,” even for its original EUA status granted just eight months prior. Given its new approval, Woodcock said that the public “can be very confident that this vaccine meets the high standards for safety, effectiveness, and manufacturing quality the FDA requires of an approved product.”