Did The FDA REALLY “Approve” The Experimental Gene Therapy Shot?

by | Aug 26, 2021 | Emergency Preparedness, Headline News | 5 comments

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    We’ve been told by the mainstream media and ruling class sociopaths that the Pfizer COVID-19 “vaccine,” that’s actually a gene therapy shot, has been “fully approved.” But is that the case? We are going to look into the wording of the letter with help from the Association of American Physicians and Surgeons.

    On August 23, 2021, the U.S. Food and Drug Administration (FDA) decided to issue an “approval decision” regarding the Pfizer-BioNTech product we all know to be an experimental gene therapy shot. Others believe this is a “vaccine” even though it doesn’t meet the definition in any legal or logical capacity.  According to the AAPS, the drug is to be marketed as Comirnaty, for individuals 16 years of age and older. The Pfizer product will continue to be available under Emergency Use Authorization (EUA) for individuals 12 through 15 years of age and for the administration of a third dose in certain immunocompromised individuals.

    So was it “fully approved?” Kind of. Unfortunately, the FDA looks like they are attempting to confuse and distract more than anything.

    A letter to Pfizer Inc. on August 23 states: “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.”

    It appears that there are two legally distinct if otherwise mostly identical products. The remaining doses of the “Pfizer-BioNTech COVID-19 vaccine” are still under an EUA and are not fully licensed. –AAPS

    The Biden Administration is already calling for mandates and wants private businesses to do the dirty work of mandating as a condition of employment, now that the prohibition against mandates on products available only under a EUA is removed. However, full approval does NOT actually apply to vials not labeled “Comirnaty.” So, yes, the “vaccine” if it’s labeled Comirnaty has received full approval from the FDA. Existing COVID-19 “vaccine” shots are still in use under the EUA though.

    Whether it is approved or not still won’t matter the ruling class. They don’t care nor do they intend to follow the laws they make the rest of us follow and that’s been more than obvious over the past several years. Still, it’s important to know just how diabolical the FDA and Pfizer and the rulers can be with their writing, speech, and actions.

    Stay alert and aware.  Read the letter yourself. We live in times where people have the attention span of a gnat and looking deeper takes time and isn’t in the best interest of the masters who own us.

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      5 Comments

      1. Like you say it is all clown show anyway.

        But for the sake of trying follow along if it does not cause damage to the brain, is the Pfizer-BioNTech COVID-19 vaccine the one that has been available to the public in the US and Israel?

        If so, who has been getting the Comirnaty vaccine? Where are the studies? How is it possible that long term studies have been performed on it? How can they approve a vaccine without doing long term studies as is the FDA protocol? Why have we not heard of it prior to the recent FDA disclosure? Where are the FDA spokespeople that we should expect to be trotted out with such an important announcement that they have bestowed their grace upon a vaccine that presumably should end the cv19 crisis? What does the FDA have to say for itself in that they made their pronouncements on the various vaccines in such a ridiculously confusing way? If Comirnaty is not available in the US where is it available? Why is it not available in the US? When do they intend to roll it out in the US? How many people have died from it? How many people have been permanently injured by it? How many miscarriages has it caused? How many children have they killed with it? How many children have they permanently injured with it? How many people have they otherwise injured with it? If the two vaccines are the exact same formulations how and why are they legally different? Why has the public not been told about its existence prior to the approval? … it would be nice if they had the courtesy to answer those questions for starters.

      2. THIS IS A TEST of the National Emergency Alert System,” “If this had been an actual emergency an official message would have followed the tone alert you heard at the start of this message. No action is required.”

      3. AT THIS POINT, THERE IS AN IMPORTANT QUESTION THAT BEGS TO BE ASKED: IF THERE IS PRESENTLY NO TEST TO DIAGNOSE COVID-19 AND ANY VARIANTS, GIVEN THE FDA’S DECERTIFICATION OF THE PCR TEST, HOW DOES THE CDC KNOW THAT THE SO-CALLED DELTA VARIANT IS SWEEPING THROUGH THE POPULATION AND IT POSES A GRAVE THREAT TO AMERICA?

        Dear America: DO NOT COMPLY. – YouTube

        Do not let media-fueled guilt trips coerce you into doing something you do not feel fully informed about.

      4. If any of you are going to do any type of lawsuit against these tyrants – the main question to ask is that they provide the COVID Idolate and the isolate for any variants. This would be in discovery in the lawsuit as you will discover their answer will be they do NOT have any meaning it doesn’t exist!

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