by Dr. Joseph Mercola, ©2022

(Sep. 21, 2022) — Just when you thought the U.S. Food and Drug Administration couldn’t possibly get any worse, they prove you wrong. Here are two recent COVID booster campaign messages tweeted out by the FDA:

“It’s time to install that update! #UpdateYourAntibodies with a new #COVID19 booster.”1 “Don’t be shocked! You can now #RechargeYourImmunity with an updated #COVID19 booster.”2

FDA Now Pushes Transhumanist Pipe-Dream

That’s right. The FDA now wants you to believe that your immune system is something that needs to be “recharged,” as if it were a battery, or “updated” with mRNA injections like a piece of software.

This is transhumanist lingo that has no bearing on real-world biology or physiology, and proves beyond doubt that the FDA is fully onboard with the transhumanist ideas of technocracy pushed by the globalist cabal. The human body is basically viewed as nothing more than a biological platform equipped with genetic software that can be altered and updated at will.

The problem, of course, is that your body doesn’t work that way. You cannot turn your body into a “bioreactor”3 or an internal “vaccine-production facility”4 and expect it to work as intended. The massive increase in disability and sudden death among COVID jab recipients is a testament to the fact that allowing Big Pharma to play God is a bad idea.

Transhumanism as a whole is a pipe-dream, as it fails to take into account just about everything that actually makes us human, including the nonlocality of consciousness, which they irrationally believe can be uploaded to a cloud-based system and merged with AI, or downloaded into an artificial body construct, such as a synthetic body.

False Advertising

The Federal Trade Commission is responsible for addressing fraudulent advertising. According to law, an ad must be “truthful, not misleading, and, when appropriate, backed by scientific evidence.”5 The FDA itself also requires drug ads to be “truthful, balanced and accurately communicated.”6

“Balanced” refers to promotional materials that include efficacy and benefit claims, which must include a balance between benefit information and information about risks. In my view, the FDA’s most recent COVID booster ads are clear examples of false advertising, because:

  • They’re not truthful and accurate, as there’s no basis for the claim that your antibodies need to be updated with a drug, or the claim that immunity must be recharged at regular intervals
  • They’re not backed by scientific evidence, as the FDA is a) ignoring massive evidence of harm from the original shots, and b) the bivalent boosters are being released based on data from a few mice alone. The FDA is advertising the boosters for the prevention of disease, even though it has zero data to prove it prevents anything
  • They’re not balanced, as the FDA fails to warn people about any of the many side effects reported to the Vaccine Adverse Event Reporting System (VAERS)7

Was No-Test Drug Approval the Plan All Along?

While I cannot prove it, I suspect Operation Warp Speed (OWS) — devised in the spring of 2020 by a dozen top officials from then-President Trump’s health and defense departments to expedite the development of a COVID-19 vaccine8 — may have been intended to normalize the approval of drugs without proper testing.

Even if the normalization of expedited drug approval wasn’t originally intended, it certainly has been used and abused to that aim since. In June 2022, the FDA quietly implemented a “Future Framework” scheme9 to speed up the delivery of COVID boosters. This is what allows for the authorization of reformulated COVID shots without human trials.10,11,12

The FDA basically rewrote the rules on the fly, deciding that mRNA gene therapies are equivalent to conventional influenza vaccines and can be updated and released without testing.

The idea here is that the safety of the mRNA COVID shots has already been proven by the original shots, which they claim have harmed or killed no one. Hence, safety is a given, and the effectiveness of reformulated boosters can be assessed simply by checking the antibody levels in a few mice, which is what Pfizer and Moderna did. 

In reality, however, millions of people around the world have been harmed and killed by the original shots, the human trials for those shots were riddled with fraud, antibody levels tell us nothing about the jab’s ability to protect against infection, and the two technologies (conventional flu vaccines and mRNA gene therapy) have no common ground.

I have no doubt this “Future Framework” will also, over time, be widened to include other vaccines and drugs that drug makers may want to tinker with. It may even lower standards for drug trials in general, which historically have required at least 10 years of multiphase testing.13 The dangers of this trend really cannot be overstated.

Analysis of US Booster Policy

In a September 12, 2022, article, Kaiser Health News raised several questions about the FDA’s authorization of the new bivalent COVID boosters:14

“… in the real world, are the omicron-specific vaccines significantly more protective — and in what ways — than the original COVID vaccines so many have already taken? If so, who would benefit most from the new shots? Since the federal government is purchasing these new vaccines … is the $3.2 billion price tag worth the unclear benefit? …


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