Posted on 08/23/2021 3:28:09 PM PDT by Enlightened1
What is going on here?
Are we being lied to?
Specifically check page 2 and page 12.
Page 2:
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. In addition, the Fact Sheet for Healthcare Providers Administering Vaccine (Vaccination Providers) was revised to provide updates on expiration dating of the authorized Pfizer-BioNTech COVID-19 Vaccine and to update language regarding warnings and precautions related to myocarditis and pericarditis. The Fact Sheet for Recipients and Caregivers was updated as the Vaccine Information Fact Sheet for Recipients and Caregivers, which comprises the Fact Sheet for the authorized Pfizer-BioNTech COVID-19 Vaccine and information about the FDA-licensed vaccine, COMIRNATY (COVID19 Vaccine, mRNA).
page 12: This product has not been approved or licensed by FDA, but has been authorized for emergency use by FDA, under an EUA to prevent Coronavirus Disease 2019 (COVID-19) for use in individuals 12 years of age and older; and • The emergency use of this product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of the medical product under Section 564(b)(1) of the FD&C Act unless the declaration is terminated or authorization revoked sooner.
https://www.fda.gov/media/150386/download
They approved a new vaccine under a different law ( BLA) called Cominarty ( the name of the new Pfizer vaxx)
but the old one ( PFizer BioNTech) was not approved. Only kept in “emergency use” until enough of the “new approved vaxx” is available.
It is designed to word play their way out of trouble. In the first paragraph it goes on to say the BLA cominarty is just a revision to the EUA (WHICH IS NOT APPROVED)
These lunatics want to please their masters, and escape culpability all in one to avoid being hanged I am guessing.
COVID-19 will be just another flu strain included in the annual flu shot by the fall of 2022. Vaccines don’t prevent exposure, they train your immune system to make antibodies to kill off the virus in the early infection stages....depending on the “viral load” of the exposure and on your personal immune system/antibody strength/health, some vaccinated people will be asymptomatic, or minor cold/hay fever symptoms, or more serious if immunocompromised...but all will have reduced symptoms and a greatly reduced chance of death.
Bmk
What the FDA did today only confuses a great deal of people in the United States...
Cominarty is what they called the PFizer mRNA shot in Europe.
The FDA said yes it can be called by Cominarty in the United States, now. Nevertheless, it is still under the EUA.
It’s all so confusing and misleading to have you believe everything is good. Mind Games.
It is illegal. Law for full approval requires public review and feedback for some period of time.
That was bypassed/ignored.
Making the approval illegal.
That’s the way I’m reading it too.
note at 9:25 according to video...i havent seen written docs, vaccines from december 2020 to march 2021 50% were placebos that means adverse reactions would have been 100% higher if there were no placebos...how about fraud? how many people thought they were vaccinated when they weren’t?
Ha! Actually the original EUA also said it “prevented” Covid. Pathetic.
Yep, you are correct.
WAR ROOM - Dr. Robert Malone on Steve’s show this am.
Suggest you see/hear his words as he laid out all pertinent
info. The approved vaccine has not yet been introduced.
Typical of d’rats. They are unable to allow truth to exit their lips.
extension eua renewed august 2021 signed by denise hint RADM fda chief scientist
https://www.thefemword.world/her-story/a-talk-with-radm-denise-hinton-fda-chief-scientist
.................................
guess who signed revocation of hydroxycholorquine eua..
https://www.fda.gov/media/138945/download
.....................................
Memorandum Explaining Basis for Revocation of Emergency Use Authorization for
Emergency Use of Chloroquine Phosphate and Hydroxychloroquine Sulfate
https://www.fda.gov/media/138945/download
https://www.fda.gov/media/138946/download
Re: 46 - I’m doubting he will take that bet, but hopefully. Never responded to defining the parameters of what constitutes winning/losing the bet.
Essentially, does some jackassin’ and makes a prediction and then goes silent. Not surprised.
It’s November. Still waiting for that nationwide, Jacobsen style, mandate. Clown.
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