Pfizer Quietly Admits it Will NEVER Manufacture the Vaccine that was FDA Approved


It’s official – Pfizer’s “fully approved” and experimental mRNA vaccine, dubbed “Comirnaty,” was nothing more than a head-fake.

Earlier this week, the notorious experimental vaccine maker quietly submitted an update to the CDC, admitting that its originally licensed “Comirnaty” vaccine will never be distributed for use.

In other words, Pfizer has exclusively been supplying its version of the experimental vaccine that was granted Emergency Use Authorization (EUA) by the FDA – aka, zero Pfizer-branded vaccines given in the US have been “fully approved.”

From the Pfizer update, via independent journalist :

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“Pfizer received initial FDA BLA license on 8/23/2021 for its COVID-19 vaccine for use in individuals 16 and older (COMIRNATY). At that time, the FDA published a BLA package insert that included the approved new COVID-19 vaccine tradename COMIRNATY and listed 2 new NDCs (0069-1000-03, 0069-1000-02) and images of labels with the new tradename. These NDCs will not be manufacturedOnly NDCs for the subsequently BLA approved tris-sucrose formulation will be produced.”

The “silent” update, which was posted –  unannounced – on the CDC’s website, comes after months of posturing by Pfizer and US public health officials, who all claimed the vaccine was “fully approved” and, therefore, you should take it.

In reality, there was as much a “fully approved” vaccine as there was proof of bigfoot – but the jab had the credentials it needed. Even more concerningly, the FDA deceptively sent out two letters regarding the separate jabs (Comirnaty and EUA) which helped confuse the public and aided in the fake-news media’s manipulation.

Until the FDA’s announcement in August 2021, Millions of Americans had been hesitant to take the vaccine because of its temporary approval status – as many as 30% of the unvaccinated, according to polling cited by Anthony Fauci at the time. Because of this, the Brandon Regime capitalized on the FDA’s decision in an effort to increase uptake and quell vaccine hesitancy, and, sadly, it worked.

Not only did the FDA’s fake approval also serve as the catalyst for a massive wave of mandates, both by Brandon federally and by Democrat tyrants alike, but the deceptive move also increased overall vaccine uptake by a massive 36% (minus the mandates), according to one study published in the Journal for American Medicine Association (JAMA).

Unsurprisingly, researchers found that series-completing vaccinations (2nd & 3rd dose etc.) saw the largest increase of all, with a 77% uptick post-‘approval’.

The FDA’s decision also sent shockwaves around the world, compelling hesitant citizens of other western nations to also take the vaccine. Millions were misled by the ‘experts.’ Is that not criminal medical malpractice, at the very, very least?

Unfortunately, any hope of accountability for this is a long shot right now. In addition to the treasonous Brandon Regime holding the keys, Pfizer is completely exempt from damages related to its experimental mRNA vaccine thanks to its status under EUA. As Dr. Robert Malone – the inventor of mRNA technology – has said for months, if Pfizer doesn’t give out its ‘fully approved’ version, they keep the immunity, and, that’s exactly what they’ve done.

From Dr. Malone:

“It’s called Comirnaty… and it’s not yet available, they haven’t started manufacturing it or labeling it, and that’s the one that the liability waiver will no longer apply to. So the one that’s actually licensed is not yet available, and when it does become available it will no longer have the liability shield. In the interim, the one that does have the liability shield is the Pfizer product.”

However, fraus omnia corrumpit (fraud corrupts all), as the saying goes. The actions of all parties involved are enough to trash any legal protections afforded to them, so, all we need are some serious people back in DC.

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