Something is very wrong: “Pfizer-BioNTech’s ‘Full Authorization’ Docs”

Monday, the U.S. Food and Drug Administration (FDA) approved a biologics license application for the Pfizer Comirnaty vaccine. Or did it…

 

The press reported that vaccine mandates are now legal for military, healthcare workers, college students and employees in many industries. New York City Mayor Bill de Blasio has now required the vaccine for all teachers and school staff. The Pentagon is proceeding with its mandate for all military service members.

But there are several bizarre aspects to the FDA approval that will prove confusing to those not familiar with the pervasiveness of the FDA’s regulatory capture, or the depths of the agency’s cynicism.

First, the FDA acknowledges that while Pfizer has “insufficient stocks” of the newly licensed Comirnaty vaccine available, there is “a significant amount” of the Pfizer-BioNTech COVID vaccine — produced under Emergency Use Authorization (EUA) — still available for use.

The FDA decrees that the Pfizer-BioNTech vaccine under the EUA should remain unlicensed but can be used “interchangeably” (page 2, footnote 8) with the newly licensed Comirnaty product.

Second, the FDA pointed out that the licensed Pfizer Comirnaty vaccine and the existing, EUA Pfizer vaccine are “legally distinct,” but proclaims that their differences do not “impact safety or effectiveness.”



There is a huge real-world difference between products approved under EUA compared with those the FDA has fully licensed.

EUA products are experimental under U.S. law. Both the Nuremberg Code and federal regulations provide that no one can force a human being to participate in this experiment. Under 21 U.S. Code Sec.360bbb-3(e)(1)(A)(ii)(III), “authorization for medical products for use in emergencies,” it is unlawful to deny someone a job or an education because they refuse to be an experimental subject. Instead, potential recipients have an absolute right to refuse EUA vaccines.


Upon a more critical look at the documents, it now very much seems to be the case that the company, along with the indispensable aid of a complicit media and the Biden administration, has engaged in a classic bait-and-switch.


U.S. laws, however, permit employers and schools to require students and workers to take licensed vaccines.

EUA-approved COVID vaccines have an extraordinary liability shield under the 2005 Public Readiness and Preparedness Act. Vaccine manufacturers, distributors, providers and government planners are immune from liability. The only way an injured party can sue is if he or she can prove willful misconduct, and if the U.S. government has also brought an enforcement action against the party for willful misconduct. No such lawsuit has ever succeeded.

Read the entire article here and here

PDF  FDA-Final_Pfizer LOA to issue with BLA approval 08.23.21_v2

The Painful Truth called the Pfizer BioNtech number 1-800-666-7248, and confirms what the author says is true.

One Reply to “Something is very wrong: “Pfizer-BioNTech’s ‘Full Authorization’ Docs””

  1. The EUA is the Emergency Use Authorization which permits issuing the ‘shot’ without any responsibility if anything goes wrong: Pfizer can’t be sued and neither can anyone else in the chain from the manufacture, distribution and administration of the ‘shot’.

    Here’s the issue: With the fully approved ‘shot’ the EUA goes away and Pfizer may be liable for all the deaths, incapacitation and other terrible side effects, which, as of the end of July are as follows according to the CDC VAERS:

    https://www.openvaers.com/covid-data (thru 7/31/21)
    Deaths 12,366
    Hospitalizations 43,046
    Urgent Care 68,040
    Office Visits 92,527
    Anaphylaxsis 4,759
    Bells Palsy 4,044
    Miscarriages 1,381
    Heart Attacks 5,236
    Myocarditis/Pericarditis 3,727
    Permanently Disabled 14,251
    Thrombocytopenia/Low Platelet 2,269
    Life Threatening 12,194
    Severe Allergic Reaction 23,357
    Shingles 7,509

    It is clear that FDA, CDC and Pfizer are playing word games to permit mandates, but the thing is, Pfizer isn’t about to provide the approved version because everyone could become liable — from the FDA, CDC, Pfizer to all businesses and medical facilities and doctors who insist you have to have it.

    Furthermore, the effectiveness is between 16% and 39% for something that over 99% of the population will survive anyway. It looks like the ‘shot’ does far more harm than the disease, doesn’t prevent the spread at all, doesn’t prevent getting the disease and may well be responsible for the variants showing up.

    It’s all about power and money — billions of dollars and being able to transform society in ways which will not be particularly beneficial:

    https://underimpressed.com/2021/07/29/its-2030-i-have-nothing-there-is-no-privacy-and-i-am/

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