100PercentFedUp.com

During the height of the COVID-19 pandemic, anyone who promoted Ivermectin was considered a conspiracy theorist and was condemned by the FDA but now a Federal court has ruled the FDA overstepped its authority when it told Americans to not use Ivermectin to fight against COVID-19.

U.S. Circuit Judge Don Willett ruled “FDA can inform, but it has identified no authority allowing it to recommend consumers ‘stop’ taking medicine.”

In one social media post, the FDA posted “You are not a horse. You are not a cow. Seriously, y’all. Stop it.”

In another post, the FDA linked to an article titled “Why You Should Not Use Ivermectin to Treat or Prevent COVID-19.”

The FDA has already approved Ivermectin as an antiparasitic drug for both humans and animals.

: 10 minutes or less.  : 11- 36 minutes.   : Over 36 min. Fun:

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• FDA Advisor Dr. Peter Doshi Explains Why Children Should NOT Receive the COVID Shot
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AmericanThinker.com

Remdesivir may be the most despised drug in American history, earning the nickname Run Death Is Near for its lethal record during COVID. Experts claimed that it would stop COVID; instead, it stopped kidney function, then blasted the liver and other organs. Now this reviled destroyer of kidneys has been approved by the FDA for COVID treatment of kidney patients. Does anybody else feel as if the FDA is shoving its power in our faces and laughing at us?

I’ve been joining online support groups for people who lost loved ones to the Remdesivir Protocol — a nightmarish sequence in which a patient is isolated in the hospital, bullied into taking Remdesivir, ventilated, and then sedated to death. Thousands of Americans were killed this way, possibly hundreds of thousands.

Editor's Note:  We have been alerting everyone to the fact that the PCR process IS NOT A DIAGNOSTIC TEST and never has been.  It is not capable of determining whether or not you have a viral infection and in fact, cannot distinguish between different types of coronaviruses as is now FINALLY being admitted to.  The CDC has known this from the very beginning and HAS BEEN LYING TO EVERYONE ALL ALONG.  The CDC, WHO, Anthony Fauci, Gates, all the usual suspects have been deliberately misleading everyone into believing the PCR test was legitimate because it IS the primary weapon they needed to create the false perception that a deadly pandemic was occurring when in fact IT HAS ALL BEEN A TOTAL LIE PERPETUATED BY A TOTALLY FRAUDULENT TESTING PROCESS.

"The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death."

The Centers for Disease Control and Prevention (CDC) announced this week that its PCR test has failed its full review and will have its Emergency Use Authorization revoked.

The Innova SARS-CoV-2 Antigen Rapid Qualitative Test, the CDC’s benchmark COVID diagnostic testing system, will be withdrawn for Emergency Use by the end of 2021 due to an inordinate frequency of false positive and negative results.

“The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death,” the FDA stated on its website.

“Labeling distributed with certain configurations of the test includes performance claims that did not accurately reflect the performance estimates observed during the clinical studies of the tests. The performance characteristics of the test have not been adequately established, presenting a risk of false results.”

TheGatewayPundit.com

In 2022, the U.S. Food and Drug Administration announced that it would limit who can receive the Johnson & Johnson/Janssen Covid-19 shot due to the serious risk of blood clots, as reported by The Gateway Pundit.

The FDA announced that it would limit the authorized use of J&J Covid-19 shot to individuals 18 years of age and older for whom other authorized or approved COVID-19 vaccines are not accessible or clinically appropriate, and to individuals 18 years of age and older who elect to receive the Janssen COVID-19 Vaccine because they would otherwise not receive a COVID-19 vaccine.

The change is being made after the investigation revealed that there is a risk of thrombosis with thrombocytopenia syndrome (TTS), a syndrome of rare and potentially life-threatening blood clots in combination with low levels of blood platelets following the administration of the Janssen Covid-19 shot.

JustTheNews.com

Federal judge said FDA tweets disparaging ivermectin "bother" him, lacking "qualifier statements" about human use. Commissioner razzed by doctors for claiming bivalents, oral antivirals have "distinct possibility" of reducing long COVID risk.

The FDA's Twitter habits are getting scrutiny in court and from medical professionals as the feds seesaw between walking back their once-confident COVID-19 assertions and making sweeping new claims without providing evidence.

Having long ago conceded that COVID vaccines can't stop viral transmission and that assertions to the contrary by President Biden among others were based on "hope" rather than science, the feds are now downplaying the influence of their social media to escape liability for allegedly violating statutory limits by interfering in medical judgments.

At the same time, over the past two months, FDA Commissioner Robert Califf has gone on a spree of evidence-free tweets about bivalent boosters and oral antivirals, such as Pfizer's rebound infection-prone Paxlovid, prompting exasperation from leading doctors.

FDA documents confirm different Pfizer EUA mRNA formulations were injected into over a hundred million Americans. US government patent shows many more mRNA bioweapon formulations

By Kyle Becker
TrendingPoliticis.com

The Food and Drug Administration’s advisery panel unanimously recommended on Wednesday that very young children be given mRNA Covid shots. The FDA panel’s move all-but-guarantees that the agency will authorize regimens of two-to-three shots for a cohort that is at statistically no risk from Covid-19.

“Outside advisers to the Food and Drug Administration voted unanimously on Wednesday to recommend that the agency authorize the Moderna and Pfizer-BioNTech coronavirus vaccines for very young children, a move that could clear the way for regulators to authorize both pediatric vaccines on an emergency basis later this week,” the New York Times reported.

TheGatewayPundit.com

America’s Frontline doctors are speaking out about FDA’s approval of Remdesivir for the treatment of COVID-19 in babies.  They are beyond shocked.

The FDA recently reported that they had approved Remdesivir for the ‘treatment’ of COVID-19 in babies.

America’s Frontline doctors can’t believe what they are seeing.