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In its approval letter to BioNTech, the FDA mandated Pfizer to submit several study results evaluating the occurrence of myocarditis (inflammation of the heart muscle) and pericarditis (inflammation of the heart’s surrounding membrane) following administration of the vaccine.

The final results of a study “entitled “A Non-Interventional Post-Approval Safety Study of the Pfizer-BioNTech COVID-19 mRNA Vaccine in the United States,” to evaluate the occurrence of myocarditis and pericarditis following administration of COMIRNATY is due October 31, 2025.

The final results of another study evaluating the occurrence of myocarditis and pericarditis following administration of the vaccine is due on September 30, 2024.

> In its approval letter to BioNTech, the FDA mandated Pfizer to submit several study results evaluating the occurrence of myocarditis (inflammation of the heart muscle) and pericarditis (inflammation of the heart’s surrounding membrane) following administration of the vaccine. > The final results of a study “entitled “A Non-Interventional Post-Approval Safety Study of the Pfizer-BioNTech COVID-19 mRNA Vaccine in the United States,” to evaluate the occurrence of myocarditis and pericarditis following administration of COMIRNATY is due October 31, 2025. > The final results of another study evaluating the occurrence of myocarditis and pericarditis following administration of the vaccine is due on September 30, 2024.

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[–] [deleted] [Sticky] • 1 pt

It is not actually approved, the EUA was simply extended and they said that is fully approved.

https://www.fda.gov/media/150386/download

On August 23, 2021, having concluded that revising this EUA is appropriate to protect the public health or safety under section 564(g)(2) of the Act, FDA is reissuing the August 12, 2021 letter of authorization in its entirety with revisions incorporated to clarify that the EUA will remain in place for the Pfizer-BioNTech COVID-19 vaccine for the previously-authorized indication and uses, and to authorize use of COMIRNATY (COVID-19 Vaccine, mRNA) under this EUA for certain uses that are not included in the approved BLA.

[–] • 1 pt

I want to sticky this comment but can't!!!

, can you help?

[–] • 1 pt

Didn't see this till now but done

[–] • 0 pt

They were going to approve it regardless. 150 million Americans have gotten at least one dose of that shit. Imagine the reaction if they didn't approve it?

[–] • 0 pt

The vaccine that they opted to not do animal testing with, because every test animal injected with it died; so they went right to injecting humans, all of which original people injected with it are now dead?

There must be some failure to communicate.

Conspiratorial genocidal malice?

Is that a real thing?

[–] • 0 pt

...all of which original people injected with it are now dead?

Say again? I've not heard anything like that.

[–] • 0 pt

Early on, both Pfizer & Moderna announced that they were bypassing animal testing, because every animal they injected died; so they went straight to human test subjects, the last of the first generation of those died last week.

If not for Operation Warp Speed, they would still be in a position of pretending the common cold, pneumonia, motorcycle accidents & shotgun blasts were deaths by CoronaVirus. Now, they can freely inject folks with the real thing.

[–] • 0 pt

the last of the first generation of those died last week.

This is the first I'm hearing of that, even here on Poal.

[–] [deleted] • 0 pt

Say again? I've not heard anything like that.

Because it hasn't killed everyone who got the jab. Yet

every test animal injected with it died

Yes they did but it took some time before all the test animals died and most of those died from ADE. These jabs use spike proteins which I am not sure they even tested on animals and appear to cause heart attacks and strokes in addition to the expected ADE...