QUACKCINE “expert” and Eugenicist Janet Woodcock, who approved Pfizer’s mRNA jab, also approved OxyContin and Fentanyl – NaturalNews.com
QUACKCINE “expert” and Eugenicist Janet Woodcock, who approved Pfizer’s mRNA jab, also approved OxyContin and Fentanyl
Janet Woodcock, the Principal Deputy Commissioner of Food and Drugs, joined the Fraudulent Drug Administration (FDA) way back in 1986. This is the woman who presided over the worst regulatory agency failure in U.S. medical history, better known as the opioid holocaust. She approved the mass use of opioid drugs without adequate evidence of safety or long-term efficacy, despite an overwhelming majority vote against this “approval” by a scientific advisory committee.
Yes, that is when OxyContin was inappropriately approved (as Woodcock later admitted) for kids as young as 11 years old. This same woman granted FULL APPROVAL of the Pfizer-BioNTech Covid quackcine just three years ago, and now THAT is the worst regulatory agency failure in U.S. medical history. Let’s take an inside look at the fraud, mayhem and quackcine holocaust taking place now, thanks to Eugenicist Janet Woodcock and her quackcine cohorts.
The most dangerous jab ever created was approved by the same person who approved the most dangerous and addictive prescription drugs for pain, ever
The year was 2021, and the world of brainwashed vaccinators were in panic mode, thanks to the fake news mass media complex and the globalist narrative of Covid-19. The approval of the clot shot that creates millions (if not billions) of microscopic spike prions in the vascular system, which invade the heart, brain, cleansing organs and ovaries, was approved and followed by employer-enforced vaccine mandates across America. This included most corporations, nearly all U.S. government jobs, and anyone who works at a hospital, school or daycare center.
That’s when all the big lies came down the pike, falsely claiming the quackcine was “safe and effective,” and that “the public can be very confident that this vaccine meets the high standards for safety, effectiveness and manufacturing quality the FDA requires of an approved product,” as quackcine expert Janet “Opioid-Queen” Woodcock said in a statement following the approval.
Woodcock is relentless in approving dangerous drugs and jabs. She never quits. She also approved a most controversial Alzheimer’s drug called Biogen (that costs patients over $50,000 per year). Woodcock is Biden’s drug and quackcine czar, who seems to be a permanently affixed drug lord for the communist regime in Washington DC.
Here’s the timeline for Woodcock’s opioid reign of terror
One would think that an FDA head that approves a drug that has maimed and killed millions of Americans would be ousted from the position, and even sued for millions or jailed, but not in the quack-drug-ridden USA. Check out this timeline of mayhem and drug terror, sponsored by the FDA’s quackcine czar, Janet Woodcock:
1995: OxyContin (oxycodone controlled-release) approved; first formulation of oxycodone that allowed dosing every 12 hours (instead of every 4 to 6 hours).
1998: Actiq (fentanyl) approved; first pain medicine approved to treat cancer breakthrough pain, but with fake “additional safety measures.”
Early 2000s: Reports of overdose and death from OxyContin rise sharply.
2001: OxyContin label changed to strengthen warnings about the drug’s potential for misuse and abuse (always too little, too late).
2003: FDA issues a Warning Letter (External Link Disclaimer) to OxyContin’s manufacturer for misleading ads. Surprise, surprise.
2011: FDA approves immediate-release of fentanyl (TIRF) products, such as Actiq.
Shortly thereafter, quack-drug-lord Woodcock issues sweeping statement that there was a massive “miscalculation about projected harms” of OxyContin, that was approved 15 years prior, by her. Yes, 15 years it took to admit it. The U.S. opioid epidemic (holocaust actually) was a decade-and-a-half deep before the FDA even began to fire up warnings.
How long before those warning flags come out for the mRNA death jabs? Will it be the year 2035, after 100 million Americans die of “unexpected” and “unexplainable” causes? Bookmark Vaccines.news to your favorite independent websites for updates on FDA-approved experimental gene therapy injections that lead directly to vascular clots, hypertension, myocarditis, pericarditis, heart attacks, strokes, PCVS, SPS and Long-Vax-Syndrome.
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