Shocker: FDA Pulling the “Approved Vaccine” Wool Over America’s Eyes

Liar’s Club Part 7

Just in time for the “vaccine mandates” the satanic cabal of the FDA and their useful idiots are trying to shove down our throats the fake Pfizer genocidal concoction being passed off as a vaccine. However, stop the press! Not so fast! It appears that the FDA is trying to pull the “approved vaccine” wool over America’s eyes!

Moreover, the FDA appears to be purposefully tricking American citizens into giving up their right to refuse an experimental product.

However, the FDA has not licensed any Moderna vaccine, nor any vaccine from Johnson & Johnson — so the vast majority, if not all, of vaccines available in the U.S. remain unlicensed EUA products.

Consequently, here’s what you need to know when somebody orders you to get the vaccine: Ask to see the vial. If it says “Comirnaty,” it’s a licensed product.

If it says “Pfizer-BioNTech,” it’s an experimental product, and under 21 U.S. Code 360bbb, you have the right to refuse.

Likewise, if it comes from Moderna or Johnson & Johnson (marketed as Janssen), you have the right to refuse.

The FDA is playing bait and switch with the American public — but we don’t have to play along. If it doesn’t say Comirnaty, you have not been offered an approved vaccine.

The Old Bait and Switch Routine

In a recent article from LeoHohmann.com titled FDA ‘playing bait and switch’ with Americans, tricking them into believing shots currently being offered have been granted full approval when they have not Leo Hohman stated:

The U.S. Food and Drug Administration’s announcement Monday that it had granted “full approval” to the Covid shots being offered by Pfizer is riddled with deceptions meant to trick the American public into thinking they have no choice but to take the jab while at the same time protecting a major pharmaceutical company from legal liability.

What was actually given full approval was a separate Pfizer-BioNtech vaccine product which goes by the name Comirnaty.

But Comirnaty is not currently available in the U.S.

This is part of a cynical plot to protect Pfizer from broad legal liability and also to snooker U.S. employers into mandating the vaccine for their employees. READ MORE HERE

The Devil is Always in the Details

However, in a follow-up article on Friday titled BOOM! Major law firm confirms FDA deceived America with its confusing ‘approval’ of Pfizer vax his claims were proven true!!!

Leo Hohmann reiterated that the “approval” given by the FDA was not for the Pfizer jab currently available in the U.S. market. The devil is always in the details. Some of us weren’t fooled.

But because we and a few others looked beneath the facade and checked the facts of what the FDA actually did and not what the media and Joe Biden’s administration said it did, we took some heat. Even some of our own subscribers questioned whether maybe we got it wrong.

No, it was the corporate media who got the story wrong.

READ LEO HOHMANN’S FOLLOW-UP ARTICLE HERE.

Liberty Counsel Press Release Confirms

On Friday, Aug. 27, 2021, Liberty Counsel, based in Orlando Florida issued a press release that confirmed the story of Leo Hohmann and others of their findings.

If you have never heard of Liberty Counsel you can visit their website to learn more ABOUT LIBERTY COUNSEL.

Liberty Counsel is a Christian ministry that proclaims, advocates, supports, advances, and defends the good news that God in the person of Jesus Christ paid the penalty for our sins and offers forgiveness and eternal life to all who accept him as Lord and Savior. Founded in 1989, Liberty Counsel has offices in Central Florida, Virginia, and Washington, D.C.

Wool Over America's Eyes Press Release

Press Release – FDA Does a Bait and Switch with COVID Shots

Aug 27, 2021

WASHINGTON, D.C. – The Food and Drug Administration (FDA) has done a bait and switch by announcing it approved its “first COVID-19 vaccine” in order to push the “vaccine” mandates and protect Pfizer pharmaceutical company from legal liability. However, there is currently no fully licensed COVID shot on the United States market. 

Current Status Summary

Albeit confusing, and probably intentionally so, this summarizes the current status of the Pfizer-BioNTech shots: 

  1. All existing Pfizer vials (in the hundreds of millions), remain under the federal Emergency Use Authorization (EUA) (meaning people have the “option to accept or refuse”);
  2. The third or “booster” Pfizer shot is identical to the above and remains under the EUA with limited use to certain categories of people;
  3. BioNTech received FDA approval for people ages 16 and above under the name Comirnaty, but there are no Comirnaty doses available in the United States;
  4. In other words, there is currently NO FDA approved COVID-19 injection available anywhere in the United States. Every COVID shot in America remains under the EUA law and thus people have the “option to accept or refuse” them; and
  5. Even when an FDA approved COVID shot becomes available, individuals are protected by federal law and many states laws from being forced to get these shots based on their sincere religious beliefs or conscience rights. 

2 Seperate Letters – 2 Separate Injections

On August 23, the FDA issued two separate letters for two separate injections. There are now two legally distinct (Pfizer vs. BioNTech), but otherwise identical products. 

The first letter is regarding FDA’s biologics license application approval for the Pfizer Inc/BioNTech COVID-19 injection which has been named Comirnaty. Yet Pfizer has not started manufacturing or labeling this drug for U.S. distribution, so it is not even available in the U.S. It is unclear whether or not it is protected by a liability shield, but web-based U.S. government communication indicates that the same program that provides compensation for COVID vaccine-related injuries will apply Countermeasures Injury Compensation Program (CICP) rather than the National Vaccine Injury Compensation Program).  At this point, there apparently has been no compensation paid to people injured by one of the COVID shots via the CICP.

The Pfizer injection, on the other hand, is still considered experimental under U.S. law. There is a legal difference between products approved under authorization of emergency use (EAU) compared with those the FDA has fully licensed. The FDA issued another letter for the existing Pfizer shots which confirms they are still under EUA, are not fully approved, and has a liability shield. 

EUA Liability Shield

EUA-approved COVID shots have a liability shield under the 2005 Public Readiness and Preparedness Act. Vaccine manufacturers, distributors, providers, and government planners are immune from liability. People who have been injured can file a lawsuit if they 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. 

That means people must be told the risks and benefits, and they have the right to decline a medication that is not fully licensed. The federal Emergency Use Authorization law and the FDA, including the FDA Fact Sheet, state unequivocally that each person has the “option to accept or refuse” the shots. In addition to federal law, the FDA includes the Nuremberg Code and the Helsinki Declaration on its website, emphasizing the fact that people cannot be forced to take experimental drugs without their full consent. 

The FDA’s approval letter to Pfizer regarding the BioNTech injection, Comirnaty, states: “Under this license, you are authorized to manufacture the product, COVID-19 Vaccine, mRNA, which is indicated for active immunization to prevent coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in individuals 16 years of age and older.” 

This letter affirms the FDA has not approved the Pfizer/BioNTech injections for the 12- to 15-year age group,

nor any booster doses for anyone. 

Regarding the Comirnaty injection

Regarding the Comirnaty injection, the FDA admits, “We have determined that an analysis of spontaneous post-marketing adverse events reported under section 505(k)(1) of the FDCA will not be sufficient to assess known serious risks of myocarditis and pericarditis and identify an unexpected serious risk of subclinical myocarditis.” 

Therefore, follow-up studies will be required with children six months to 15 years as well as six studies for up to five years regarding the adverse effects of myocarditis and pericarditis. 

In addition, the FDA bypassed and disregarded the normal advisory committee and public comment process for this license.  

The letter states, “We did not refer your application to the Vaccines and Related Biological Products Advisory Committee because our review of information submitted in your BLA, including the clinical study design and trial results, did not raise concerns or controversial issues that would have benefited from an advisory committee discussion” (emphasis added). 

The FDA also acknowledges that while Pfizer-BioNTech has “insufficient supplies” (in other words, it is not currently available on the U.S. market) of the newly licensed Comirnaty vaccine actually available. However, the letter also states there is “a significant amount” of the Pfizer-BioNTech shots which has been produced under the EUA and will continue to be offered under the same EUA status.

Can be Used “Interchangeably”?

In its approval letter, the FDA specifies the Pfizer shot under the EUA should remain unlicensed, is still available for use, and can be used “interchangeably” with the newly licensed Comirnaty product. According to the FDA, the newly licensed Comirnaty injection and the existing Pfizer shot, while “legally distinct,” are not any different in terms of their “safety or effectiveness.” 

Despite whether these COVID shots are licensed or not, they cannot be mandatory under Title VII. In general, employee vaccine religious exemption requests must be accommodated, where a reasonable accommodation exists without undue hardship to the employer, pursuant to Title VII of the Civil Rights Act of 1964. Many people hold sincere religious beliefs against taking the COVID shots or taking those derived from or which used at any stage of the development aborted fetal cell lines. 

Read the Complete Liberty Counsel unedited press release HERE

News

Other Related Articles

American Thinker – Did the FDA Pull a Bait-and-Switch on the American People?

Children’s Health Defense – 2 Things Mainstream Media Didn’t Tell You About FDA’s Approval of Pfizer Vaccine

New American – Children’s Health Defense to Challenge Full Approval of Pfizer COVID Vaccine

Children’s Health Defense (CHD) is challenging the Food and Drug Administration’s “premature, arbitrary, and capricious” approval of the Pfizer-BioNTech COVID vaccine for people aged 16 and up.

On Monday, the FDA announced the Pfizer-BioNTech COVID-19 vaccine will be marketed as Comirnaty, protecting against COVID for those aged 16 and up. Individuals between ages 12 and 15 may continue to get the vaccine, but it remains approved only under emergency use authorization currently.

Immediately following this announcement, CHD announced it intended to challenge the agency’s decision. CHD president Mary Holland accused the agency of putting the interests of the pharmaceutical industry over Americans.

With over 13,000 reported deaths from COVID shots, we are deeply concerned about the impact on health, both short- and long-term,” she said. “We intend to challenge this approval and licensure. We do not believe that this approval will significantly affect the trajectory of the pandemic, as we know that these shots are less than 50% effective against the variant in circulation now.”

According to LifeSite News, the 13,000-plus deaths following the COVID vaccination are “more deaths than all [post-vaccination] deaths reported during the entire 30-year history of the federal reporting system.”

READ THE FULL ARTICLE HERE.

VIDEO – Dr. Malone Sounds Alarm On Liability Coverage Of Pfizer Vax

Be Sure to Watch the VIDEO Below to Fill in the Blanks

Liars Club Relabeling Adverse Effects as “Vaccine” Breakthrough Variants!

I posted this article earlier today which included the interview between Steve Peters and Karen Kingston. It will fill in many blanks for you!

Karen Kingston is a former Pfizer employee, a pharmaceutical marketing expert, and a biotech analyst. In the following 30 minute video, Karen Kingston reveals many earth-shattering revelations. One of which is how the Liars Club is Relabeling Adverse Effects as “Vaccine” Breakthrough Variants. Why? The satanic globalists need to continue pushing the false narrative of the satanic destruction of America through the Covid Plandemic! The ultimate goal being the placement of the ruler of their choice over the entire world. However, we can rejoice because God our Conqueror sees EVERYTHING. Therefore, BE ENCOURAGED!

You can watch the 30-minute video HERE.

Maranatha!

ABC’s of Salvation – Repent and be saved from the Wrath of God to come.
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