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The FDA Has Become a Vaccine Marketing Unit

Congress no Will to Call for Market Removal, Mass Vaccination Campaign Rolls On

By Peter A. McCullough, MD, MPH

Most of my patients have not had a COVID-19 vaccine or booster since 2021. When I go in CVS or Walgreens, I rarely see a sullen vaccine recipient in the back waiting for a reaction to one of the hopeless XBB.1.5 boosters. I was asked on February 2, 2024, more than three years the failed campaign, I was asked on Outside the Beltway with John Fredericks “why is the government still pushing vaccines?”

I told him that the FDA has essentially become a marketing unit for Pfizer Moderna. The FDA should be an unbiased regulator protecting Americans from drug safety issues. Instead Commissioner Robert Califf, MD, and Peter Marks, M.D., Ph.D. the director of the Center for Biologics Evaluation and Research (CBER) at the Food and Drug Administration have been promoting boosters. Under no circumstances should the FDA promote the use of any drug or vaccine.

Most members of Congress are vaccinated (72% in 2021) and are having a very difficult time coming to grips with the personal psychological regret of what they have done to themselves, potentially their families, and constituents. You can readily identify this when striking up a conversation on vaccine safety getting the quick retort “I don’t want to talk about it.”


Enjoy this brief update on the vaccine debacle on Real America’s Voice, Outside the Beltway hosted by John Fredericks.


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Peter A. McCullough, MD, MPH

President, McCullough Foundation

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