‘Updated’ Covid-19 Booster Shot Gets “Emergency Authorization” Without Ever Being Tested on Humans

They. Just. Don’t. Stop.

The Vaxxed Are Dropping Like Flies

Before Democrats took over our healthcare system, vaccines used to take 12 to 15 yrs to go from development to public release – after long term studies of the effects on humans.

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Reformulated Covid-19 Booster Shot Gets “Emergency Authorization” Without Ever Being Tested on Humans

By Brian Lupo, The Gateway Pundit, August 31, 2022:

The federal government and mockingbird media are still clinging to their slipping grasp of the dwindling minority of Americans who are still concerned about the “pandemic”.

Reported by the USAToday:

The FDA gave emergency authorization to a “bivalent” vaccine that targets both the original virus and the BA.4 and BA.5 variants that now dominate the world…

As requested by the companies, the Pfizer-BioNTech booster was authorized for anyone ages 12 and up, while Moderna’s vaccine is authorized for adults only. Both were authorized for use at least 2 months after any previous COVID-19 shots.

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The new vaccine, which is actually called Bivalent, is still not the FDA-approved Cominarty, which is Pfizer’s only FDA-approved COVID-19 vaccine.  In fact, USAToday claims this modified vaccine is “bivalent”, but the FDA specifically confirms that Cominarty is a monovalent vaccine.

The new COVID boosters were not tested on humans – only mice.

Furthermore, that same FDA webpage lists Cominarty as:

a monovalent COVID-19 vaccine that is approved for use as a two-dose primary series for the prevention of COVID-19

and then immediately underneath it, the FDA states:

Pfizer-BioNTech COVID-19 Vaccine is a monovalent COVID-19 vaccine that is authorized for emergency use to prevent COVID-19

and then in another semantics pretzel, they introduce Bivalent:

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Pfizer-BioNTech COVID-19 Vaccine, Bivalent is authorized for use to prevent COVID-19 in individuals 12 years of age and older

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