CHD to sue FDA for ‘capricious’ approval of COV vaccine

2
262

Following the announcement this week of approval for a shot, fraudulently labeled as a vaccine, that isnโ€™t even on the market in the United States, Robert F. Kennedyโ€™s Childrenโ€™s Health Defense will be filing a lawsuit against the FDAโ€™s โ€œpremature, arbitrary, and capriciousโ€ approval of the Pfizer-BioNTech COVID vaccine for people aged 16 and up.

 

Monday, the U.S. Food and Drug Administration (FDA)ย approvedย aย biologics license applicationย for the Pfizer Comirnaty vaccine.

It’s similar to what Justice Roberts did, it’s tax here but not a tax there. In the vaccine’s case, it’s approved for mandated use, but it’s experimental for purposes of suing them.

There are insufficient supplies of Comirnaty so the FDA decided the Pfizer-BioNTech will continue as EUA, aka experimental and unlicensed, and can be used in Comirnatyโ€™s place.

The FDA said the vaccines are ย โ€œlegally distinct,โ€ but proclaims that their differences do not โ€œimpact safety or effectiveness.โ€

Experimental drugs cannot be mandated and are immune from liability compared with FDA-approved drugs.

The government has a stingy compensation program for experimental drugs and thatโ€™s it.

At least for the moment, the Pfizer Comirnaty vaccine has no liability shield. Licensed adult vaccines, including the new Comirnaty, do not enjoy any liability shield.

The FDA approval led to the government and organizations mandating the vaccines, which was the clear goal of the bait-and-switch scheme.

Robert F. Kennedy and Dr. Meryl Nass wrote the following:

Given this background, the FDAโ€™s acknowledgment in its approval letter that there are insufficient stocks of the licensed Comirnaty, but an abundant supply of the EUA Pfizer BioNTech jab, exposes the โ€œapprovalโ€ as a cynical scheme to encourage businesses and schools to impose illegal jab mandates.

The FDAโ€™s clear motivation is to enable Pfizer to quickly unload inventories of a vaccine that science and theย Vaccine Adverse Events Reporting Systemย have exposed as unreasonably dangerous, and that theย Delta variantย has rendered obsolete.

The government couldnโ€™t win the argument so they had to โ€œabolish the public process and independent oversight,โ€ write the authors.


Subscribe to the Daily Newsletter

PowerInbox
0 0 votes
Article Rating
2 Comments
Most Voted
Newest Oldest
Inline Feedbacks
View all comments