2 Things MSM Didn’t Tell You About FDA’s Approval Of Pfizer Vaccine | Children’s Health Defense

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Monday, the FDA approved a biologics license application for the Pfizer Comirnaty vaccine.

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

By Robert F. Kennedy, Jr. Meryl Nass, M.D. | Children’s Health Defence

Buried in the fine print of Monday’s approval by the U.S. Food and Drug Administration of the Pfizer Comirnaty COVID vaccine are two critical facts that affect whether the vaccine can be mandated, and whether Pfizer can be held liable for injuries.

Monday, the U.S. Food and Drug Administration (approved a biologics license application for the Comirnaty vaccine.

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 approval that will prove confusing to those not familiar with the pervasiveness of the ’s regulatory capture, or the depths of the agency’s cynicism.

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

The  decrees that the -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 pointed out that both the licensed Comirnaty vaccine, and the existing vaccine are “legally distinct,” but proclaims that their differences do not “impact safety or effectiveness.”

There is a huge real-world difference between products under an EUA compared with those that 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 .

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

EUA-licensed 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.

The government has created an extremely stingy compensation program, the Countermeasures Injury Compensation Program, to redress injuries from all EUA products.

The program’s parsimonious administrators have compensated under 4% of petitioners to date — and not a single COVID vaccine injury — despite the fact that physicians, families and injured vaccine recipients have reported more than 600,000 COVID vaccine injuries.

At least for the moment, the Comirnaty vaccine has no liability shield. Vials of the branded product, which say “Comirnaty” on the label, are subject to the same product liability laws as other U.S. products.

When the Centers for Disease Control and Prevention’s () Advisory Committee for Immunization Practices places a vaccine on the mandatory schedule, a childhood vaccine benefits from an generous retinue of liability protections.

But licensed adult , including the new Comirnaty, do not enjoy any liability shield. Just as with Ford’s exploding Pinto, or Monsanto’s herbicide Roundup, people injured by the Comirnaty vaccine could potentially sue for damages.

And because adults injured by the vaccine will be able to show that the manufacturer knew of the problems with the product, jury awards could be astronomical.

is therefore unlikely to allow any American to take a Comirnaty vaccine until it can somehow arrange immunity for this product.

Given this background, the ’s acknowledgement in its approval letter that there are insufficient stocks of the licensed Comirnaty, but an abundant supply of the EUA BioNTech jab, exposes the “approval” as a cynical scheme to encourage businesses and schools to impose illegal jab mandates.

The ’s clear motivation is to enable to quickly unload inventories of a vaccine that science and the Vaccine Adverse Events Reporting System have exposed as unreasonably dangerous, and that the Delta variant has rendered obsolete.

Americans, told that the COVID vaccine is now licensed, will understandably assume COVID vaccine mandates are lawful. But only EUA-authorized , for which no one has any real liability, will be available during the next few weeks when many school mandate deadlines occur.

The appears to be purposefully tricking American citizens into giving up their right to refuse an experimental product.

While the media has trumpeted that the has approved COVID , the has not approved the BioNTech , nor any COVID for the 12- to 15-year age group, nor any booster doses for anyone.

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

Here’s what you need to know when somebody orders to get the vaccine: Ask to see the vial. If it says “Comirnaty,” it’s a licensed product. If it says “-BioNTech,” it’s an experimental product, and under 21 U.S. Code 360bbb, you have the right to refuse.

If it comes from or (marketed as Janssen), you have the right to refuse.

The 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.

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

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