Taking Back Our Stolen History
HISTORY HEIST
Food and Drug Administration (FDA)

Food and Drug Administration (FDA)

The Food and Drug Administration (FDA) is an executive branch agency, the beneficiary of vast legislative powers delegated to it by Congress. It is also the repository of powers not delegated by Congress that FDA has usurped beyond the limits of its enabling statute throughout its 68 year history. The Commissioner of FDA sits at the pleasure of the President. The FDA is one of the largest and most powerful federal bureaucracies. It regulates over $1 trillion dollars of goods. The products under its jurisdiction account for 25 cents of every dollar spent by American consumers. FDA has approximately ten thousand employees and 26 district offices across the United States. The United States Attorneys and federal marshals are at its disposal and can obtain search and seizure warrants to be exercised without any advance notice against any company that sells a food, dietary supplement, drug, or medical device in the United States.

To understand how FDA has acquired so much power in a government designedly of limited powers, we have to appreciate the agency’s place in history. Indeed, we have to start with the origins of American constitutional government, 151 years before the FDA came into existence, to appreciate the perversion of the Framers’ plan effected by the modern FDA. We must follow America’s late 18th Century rejection of the arbitrary will of King George III, its embrace of a written Constitution where the law and a system of separation of powers and checks and balances were supposed to prevent the accumulation of tyrannical power in any one set of hands. We must then observe the rise of independent regulatory commissions in the Twentieth Century and how those commissions united legislative, executive, and judicial powers into single hands in violation of our founding principles. We must then come to see how FDA in particular exemplifies the arbitrary rule of people in power over the rule of law.

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Chronological History of Events Involving the FDA

Pfizer Document Dump Shows Doctor With Ties to Gates Foundation Deleted Trial Participant’s Vaccine Injury

Pfizer Document Dump Shows Doctor With Ties to Gates Foundation Deleted Trial Participant’s Vaccine Injury

An 80,000-page cache of Pfizer-BioNTech COVID-19 vaccine documents released by the U.S. Food and Drug Administration (FDA) sheds light on Pfizer’s extensive vaccine trials in Argentina, including the unusually large size of the trials and the story of a trial participant whose vaccine reaction was “disappeared.” The case of Augusto Roux in Argentina suggests that in at least one instance, a trial participant whose symptoms were determined to be connected to ...
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GAO Whistleblower Report: CDC and FDA 'altered' Covid guidance and even 'suppressed' findings

GAO Whistleblower Report: CDC and FDA ‘altered’ Covid guidance and even ‘suppressed’ findings

CDC and FDA officials 'altered' Covid guidance and even 'suppressed' findings related to the virus due to political pressure, a bombshell report suggests. Investigators from the watchdog Government Accountability Office (GAO) spoke to more than a dozen directors and managers who worked at the agencies behind the country's pandemic guidance. They unearthed allegations of 'political interference' in scientific reports, raising fears that research was tampered with. In its 37-page ...
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FDA Approves Remdesivir for “Treatment” of Covid-19 in Babies as Young as 28 Days Old

FDA Approves Remdesivir for “Treatment” of Covid-19 in Babies as Young as 28 Days Old

America’s Frontline doctors couldn’t believe it. On April 25, 2022, the failed Ebola drug Remdesivir was approved by the FDA for “treatment” of Covid-19 in babies as young as 28 days old and as small as seven pounds! This is the exact same drug that has been wreaking carnage throughout hospitals since Fauci and Company approved the rigid CARES Act hospital protocol, along with bonus payments ...
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FDA Launches Investigation Into Popular Breakfast Cereal After Numerous Reports of People Falling Ill

FDA Launches Investigation Into Popular Breakfast Cereal After Numerous Reports of People Falling Ill

The U.S. Food and Drug Administration has reportedly opened an investigation into Lucky Charms Cereal after hundreds of people have filed reports claiming to have gotten sick after eating it. Some of the most common side effects that have been reported by consumers include nausea, diarrhea, and vomiting after eating the extremely popular snack, according to hundreds of incident reports submitted online to the food safety ...
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Judge Unseals Pfizer Docs They Wanted Sealed for 75 Yrs. 42,000+ Adverse Events; 1200+ Deaths in First 3 Months

Judge Unseals Pfizer Docs They Wanted Sealed for 75 Yrs. 42,000+ Adverse Events; 1200+ Deaths in First 3 Months

Pfizer wanted you to wait until the year 2085 to know the vaccine has NINE pages of side effects (1291 adverse reactions and counting)… The new Pfizer data dump shows 42,000+ adverse effects including 1,200+ deaths caused by the vaccine just in the first 3 months of use (1-Dec-20 to 28-Feb-21), and the FDA didn’t withdraw it from the market! How about the 9400 unknown outcomes! 22% unknown ...
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