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Popular COVID Drug Manufactured by Merck is Causing “Unintended” Virus Mutations, Potentially Fueling COVID’s Spread


 

TheGatewayPundit.com

An international team of researchers has determined that a popular drug manufactured by Merck to treat COVID-19 is driving what is being described as “unintended” mutations in the virus and potentially fueling the virus’s spread

The Express reported Monday that these researchers studied a whopping 15 million COVID-19 sequences to determine how it has mutated over time. What they found could be described as alarming.

Their analysis shows that there were mutations that deviated from the normal pattern of change. Moreover, one-third of the mutations were associated with individuals who had taken the popular antiviral drug molnupiravir.

Molnupiravir is produced by Merck and Ridgeback Biotherapeutics. It was one of the first antiviral placed on the market to combat COVID-19 and is used by patients in several countries including the United States.

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Video: The CDC Has No Authority To Make Decisions For Americans


NaturalNews.com

The Centers for Disease Control and Prevention (CDC) has no authority to make decisions for Americans. This was the contention of health freedom advocate Leslie Manookian when she joined host Dr. Daniel Bobinski in the April 21 episode of "Keep the Republic" on Brighteon.TV.

"CDC is supposed to be an agency that provides guidance and recommendations, not issuing edicts and directives to 330 million people. And so if you look at the CDC vaccination schedule, it's recommended, it's up to the states to decide what they will do with respect to those," said Manookian, founder of the Health Freedom Defense Fund (HFDF).

"And what this really comes down to is constitutional authority. Health powers are reserved to the states; they're not given to the federal government. And so the CDC, as a federal health agency under the executive, doesn't have the authority to make these kinds of decisions for everybody. That said, the administrative state has gained a lot of power. Whether it's constitutional and right or not is another question."

Manookian, a former Wall Street business executive and award-winning documentary film producer, said she founded HFDF because she was very concerned about all the Wuhan coronavirus (COVID-19) measures and the egregious violations of basic American liberties.

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Video: Big Pharma’s Stranglehold on American Society Has Worsened


NaturalNews.com

Big Pharma’s stranglehold on American society has worsened, according to activist and film producer Leslie Manookian.

She put forward this argument during an appearance on the “Health Ranger Report,” which also had film director and producer Kendall Nelson as a guest. The two are collaborating on the documentary movie “The Greater Good.”

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Science Fraud: Pfizer’s Covid Jab “Placebo” Control Group Was Given Moderna’s “Vaccine”


 

SHTFPlan.com

Pfizer has committed a major scientific fraud. Instead of giving a control group a placebo, they were instead given Moderna’s mRNA “vaccine.” The problem is, that’s no longer a control group, and the data was presented as if they were given a placebo or a “treatment that has no therapeutic valuce, such as water, or saline.”

New research published at Preprints.org reveals that the so-called “placebo” injections used in Pfizer’s Wuhan coronavirus (COVID-19) “vaccine” trials were not real placebos. Moderna’s “vaccine” has some kind of effect on the body, or the ruling class wouldn’t insist the slaves be injected with it.

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Judicial Watch: Records Reveal Pfizer Tested Safety of Covid Vaccine Booster on 23 People Before Biden FDA Approved the Shots


 

TheGatewayPundit.com

Judicial Watch on Thursday released a tranche of records revealing Pfizer tested the safety and efficacy of the Covid vaccine booster on only 23 people in 2021 before it asked the FDA to approve the shots.

Biden’s FDA immediately approved the Covid booster shot at the end of September of 2021.

“The participants included 11 people aged 18 to 55 and 12 people aged 65 to 85. Of the younger group, there were nine females and two males; eight of whom were white, one was black and two were Asian. Of the older group six were female, six were males, and all were white.” Judicial Watch reported.

8.9 million Covid boosters were administered just three weeks after the FDA approved the shots.

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South African High Court Rules “Secret” Covid Vaxx Contracts Between Govt & Big Pharma Must Be Made Public

What was done in the dark is being brought to the light!


 

Infowars.com

A document released Thursday by South Africa’s North Gauteng High Court in Pretoria shows a judge has ordered the “secret” Covid-19 “vaccine” contracts between the nation’s government and Big Pharma companies be made public.

Following the ruling, South Africa’s National Department of Health has a 10-day window to release the documents detailing the contracts.

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Anthem Medical’s Vaxx-Incentive Plan Exposes How Much Doctors Got Paid to Push the Death Jabs


 

TheLibertyDaily.com

Following the rollout of the Covid-19 “vaccines,” there was a hardcore push by people in authority to get as many men, women, and children jabbed as many times as possible. Politicians and bureaucrats made threats and restricted those who refused. Journalists gaslit us. Celebrities ridiculed us. It has only been in the last few months that the pressure campaign has let up a bit, but it’s still there in the background.

While most Americans have a healthy distrust for politicians, corporate media, and Hollywood stars, a strong majority of people got jabbed anyway for one huge reason: Most doctors were on board with the mass-vaccination program. Many might laugh when Bill de Blasio or Sean Hannity advise us to get jabbed, but with so many doctors echoing the sentiment, millions if not tens of millions dismissed their better judgment based on recommendations from medical professionals.

 

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Evidence of How Far Vaccine Companies Are Willing to go to Hide Evidence of Their Product Killing Babies


The Wyeth (now Pfizer) DTP Vaccine Memo

Evidence of how far vaccine companies are willing to go to hide evidence of their product killing babies. Wyeth was bought by Pfizer in 2009.

 

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This document should be considered substantial precedent in knowing just how far these corporations are willing to go in attempts to cover up and obfuscate the harm their products can cause.

In this case, the harm was numerous cases of SIDS (sudden infant death syndrome) that happened in a cluster in Tennessee after use of the DTP vaccine made by Wyeth in the 1970s.

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'It's Murder': Remdesivir Victims Decry FDA's Shocking New Move


 

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.

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Video: Former Big Pharma Exec Blows the Whistle on Bad Batches of the Covid "Vaccine"


Sasha Latypova, former Pharmaceutical Executive, collected vaccine injury reporting data and discovered that not all batches of COVID vaccines were the same as we were all led to believe.  Some specific batches showed a severe lack of good manufacturing practice compliance which produce very little variability between batches of medications being produced.  What Sasha found was the COVID vaccines had a HUGE VARIABILITY between batches with regards to injury reports which, of course, the CDC and FDA lied about it.   

 

 

 
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