Give it a Rest: Reformulated Covid-19 Booster Shot Gets “Emergency Authorization” Without Ever Being Tested on Humans


by Brian Lupo, The Gateway Pundit:

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.

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:

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:

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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