Some food for thought…
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.
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.
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.
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 Pfizer 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 (CDC) Advisory Committee for Immunization Practices places a vaccine on the mandatory schedule, a childhood vaccine benefits from a generous retinue of liability protections.
But licensed adult vaccines, including the new Comirnaty, do not enjoy any liability shield. 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.
Given this background, the FDA’s acknowledgement 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 “approval” as a cynical scheme to encourage businesses and schools to impose illegal jab mandates.
Americans, told that the Pfizer COVID vaccine is now licensed, will understandably assume COVID vaccine mandates are lawful. But only EUA-authorized vaccines, for which no one has any real liability, will be available during the next few weeks when many school mandate deadlines occur.
The FDA appears to be purposefully tricking American citizens into giving up their right to refuse an experimental product.
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.
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.
Karen Kingston is a former Pfizer employee, a pharmaceutical marketing expert and biotech analyst.
Kingston joins Stew Peters, and brings the receipts! Kingston reveals how the FDA “approval” is sure to be the “checkmate” move to end the shots that have caused unprecedented injury and death, worldwide.
Keep in mind that these “vaccines”, their components are made in China; the country in which the virus originated. The same country whom is building an alliance with the Taliwackers in Afghanistan.
What does this mean?
Judicial Watch announced today that it received 129 pages of records from the Department of Health and Human Services (HHS) which include “urgent for Dr. Fauci ” email chain which cites ties between the Wuhan lab and the taxpayer-funded EcoHealth Alliance. The government emails also report that the foundation of U.S. billionaire Bill Gates worked closely with the Chinese government to pave the way for Chinese-produced medications to be sold outside China and help “raise China’s voice of governance by placing representatives from China on important international counsels as high level commitment from China.”
The new production of records also includes a January 6, 2020, “Wuhan Pneumonia Update” report which details how Peter Daszak, president of EcoHealth Alliance, was tied to the Wuhan lab and was “funded for work to understand how coronaviruses evolve and jump to human populations.”
Speaking of pneumonia, there’s an interesting meme making its rounds on social media.
The meme while I knew wasn’t completely accurate made me wonder…where there’s smoke, there’s fire. So I found the report the meme alluded to. If you’d like to read it – the link is in the caption below.
The report is only 9 pages long…the thing I found most interesting…the conclusions.
“…If severe pandemic influenza is largely a problem of viral-bacterial copathogenesis, pandemic planning needs to go beyond addressing the viral cause alone (e.g., influenza vaccines and antiviral drugs). Prevention, diagnosis, prophylaxis, and treatment of secondary bacterial pneumonia, as well as stockpiling of antibiotics and bacterial vaccines, should also be high priorities for pandemic planning.”
So WHY is Dr. Faux-ci backtracking and demanding we all be vaccinated against the COVID-19 virus? Why hasn’t he implemented his findings in his 2008 report? Antiviral drugs? Antibiotics? Bacterial vaccines?
Have the FDA & CDC whored themselves out to the massive monopoly of big pharma?
Open Letter to the FDA:
Thank you for telling us the risk of coconut oil and recommending GMO canola oil instead. Synthetically processed oils over natural G-d given coconut oil. Whew! Close call! Almost ate something healthy, there!
Thank you for recommending Frosted Flakes over fruit! Of course, dead food in a box coated in sugar would be healthier than enzymes and fiber rich, nutrient dense, delicious fruit. What was I thinking!?
Thank you for the blessing of artificial sweeteners! We now know of their toxic effects on the brain and ability to cause cancer. Man, if we would have simply stuck to all natural G-d-given sweeteners, the pharmaceutical companies would have gone out of business. Can’t have that!
Thank you for processed dairy loaded with hormones and antibiotics! It does a body good… even the 7 year olds with breast buds and behavioral issues….. we thank you!
Thank you for Red Dye #40 and Yellow #5 linked to cancer and proven to cause hyperactivity in kids… we mom’s especially thank you. Big hugs on that one. How else would our kids eat their food if it wasn’t brightly colored?!
Thank you for all the synthetic preservatives, additives, BHT, palm oil, high fructose corn syrup, TBHQ, and so many others… so that our food can last on the shelf for up to 20 years. Awesome!
It feels soooooo GOOD to have a government agency that is NOT influenced by special interest money, that simply looks out for the “greater good” of America and the health of the people.