The Reason They Want to Give Covid Jabs to Kids

image credit: vecteezy.com

At NOQ, Dr Joseph Mercola summarizes the report by Oscar Mayer heiress Alix Mayer:

STORY AT-A-GLANCE

• The reason our children are being targeted by COVID mandates is because vaccine makers want to get the shots onto the childhood vaccination schedule
• Once a vaccine is added to the childhood schedule, the vaccine maker is shielded from financial liability for injuries, unless the manufacturer knows about vaccine safety issues and withholds that information
• Products must satisfy four criteria in order to get emergency use authorization: There must be an emergency; a vaccine must be at least 30% to 50% effective; the known and potential benefits of the product must outweigh the known and potential risks of the product; and there can be no adequate, approved and available alternative treatments (drugs or vaccines). Unless all four criteria are met, EUA cannot be granted or maintained
• According to a U.S. federal court decision, the Pfizer shot and BioNTech’s Comirnaty are not interchangeable
• Comirnaty is not fully approved and licensed. It’s only “ready for approval.” Comirnaty is licensed to be manufactured, introduced into state commerce and marketed, but it’s not licensed to be given to anyone, and it’s not yet available in the United States. They’re waiting for it to be added to the childhood vaccination schedule, to get the liability shield.

In this interview, Alix Mayer explains why our children are being so aggressively targeted for the COVID-19 injection even though they’re not at risk of serious SARS-CoV-2 infection, and clarifies the status of Comirnaty.

Mayer, board president of Children’s Health Defense —California Chapter, is herself vaccine injured; not from the COVID jab, but from a series of vaccines she received 20 years ago. (On a side note, her great-great-grandfather was Oscar Mayer, founder of the Oscar Mayer company, which the family sold to General Foods in 1981.)

Mayer graduated from Duke University with a BA and from Northwestern University with an MBA in finance and management strategy. She worked for Apple in the mid-1990s. When she was 29, Apple promoted her to acting manager of worldwide customer research.

In preparation for a family trip to Bali, her doctor recommended getting six vaccines: hepatitis A vaccine, hepatitis B vaccine, diphtheria, tetanus, polio and oral typhoid, which she did. Eventually, 13 years later, she finally realized it was these shots that triggered her health problems.

Full report is here. 

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“The FDA did NOT grant full approval to the Pfizer shots”

 

image:  Disney's Pinnochio

I continue to post updates on the COVID crisis because it is threatening our basic freedoms.  While some states have banned vaccine mandates, such as Texas, Ohio has not yet voted. And now we are being told that the FDA has given its full approval to the Pfizer vaccine.  I’ve already asked how long-term effects can be studied when there has not been a long-term testing period.  So below is an extract from Carl Schwitzer’s “The FDA did NOT grant full approval to the Pfizer shots” at AmericanThinker:

You may have heard that the Pfizer-BioNTech COVID-19 shot received FDA approval this past Monday.  Politicians, national health officials, and journalists are breathless with excitement about how this approval will finally induce the remaining "vaccine-hesitant" into stepping forward to receive their jab.  The FDA even has a press release on its website about it.

There's just one problem.

If you read the actual letters that the FDA sent to Pfizer on August 23, 2021, you'll see that the FDA did no such thing.  In the sense that the term "FDA approval" is generally understood, this drug is not approved by the FDA.  It is still under EUA (Emergency Use Authorization).  It is still an experimental drug.

The FDA sent two letters.  The first one was a letter of BLA (Biologics License Application) approval, and the second was a letter of EUA extension to COMIRNATY.

The BLA approval letter approves Pfizer's application for a license to label its COVID-19 drug with the brand name COMIRNATY.  This letter also spells out the terms and requirements for nine additional clinical trials over five years [my emphasis], and yearly status reports, to study the acknowledged occurrences of myocarditis and pericarditis that have followed the administering of the Pfizer shots.  This license to label and manufacture is not a full approval of the drug, which clearly is still subject to many years of clinical trials [my emphasis].

The EUA extension letter extends the term of the EUA for the current drug and authorizes (licenses) the experimental use of the brand-name drug COMIRNATY.  In the first paragraph on page 2, this letter references the license approval letter.  In the second paragraph on page 2, the August 12 EUA is re-issued to include the name-branded drug in the emergency use authorization, and to add "language regarding warnings and precautions related to myocarditis and pericarditis."  In the last paragraph on page 4, the EUA nature of the drugs is re-iterated, and COMIRNATY is additionally authorized for use for individuals aged 12 through 15 years.

The mRNA gene therapy shots are still experimental.  Mandating them is still wrong — by a wide variety of ethical standards.

Dr. Meryl Nass, M.D. found the truths that the FDA buried in the blather of these letters and offers a theory about why it was done this way.  The drug-manufacturers were granted immunity from liability for the drugs produced under the EUAs.  The granting of the license re-applies the customary liability for injury and death caused by the product.  Pfizer, the health officials, and the politicians get to take a fictitious victory lap for the "approval," while Pfizer-BioNTech continues to stealthily enjoy immunity from product liability because there are many millions of the unlicensed doses on the shelves and in the manufacturing pipeline that will be administered first.  The licensed version will not arrive on shelves or be jabbed into arms for many months to come.

. . .

The rest of the column is here. Becker News has another report on the same subject.  I am linking here, as the analyses are a bit difficult to follow, and a second report may help to clarify.  One thing is clear: we are being lied to again.

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