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Fauci’s Inquisition Against Safe and Effective Anti-COVID-19 Drugs

By Richard Gale and Dr. Gary Null | Global Research | April 6, 2024

A question needs to be asked. Were the novel experimental drug treatments for SARS-CoV-2 viral infections that Anthony Fauci, the CDC and FDA advocated for and funded responsible for worsening the contagion and countless deaths?

However, at that time there were plenty of studies confirming there were pre-existing safe, inexpensive medications known to have highly effective antiviral properties to treat Covid-19 patients. Among these were ivermectin and hydroxychloroquine (HCQ).

There were also specific nutrients such as vitamin D and zinc, known to strengthen the immune system against viral infection and yet there was no recommendation from the government about the benefits of proper nutrition. So why did Fauci along with other federal health officials choose to intentionally ignore the scientific evidence and rather condemn these repurposed drugs? In Fauci’s case, over a year and half into the pandemic, he continued to lie outright on CNN that “there is no clinical evidence whatsoever that [ivermectin] works.”[1] And could millions have been saved if these generic medications were prescribed rather than the feds doing nothing but recommending social isolation and quarantines as the world awaited an experimental Covid-19 vaccine to enter the market?

To date, between ivermectin and HCQ alone, there have been 670 published studies, analyses and papers involving over 9,800 scientists and over 682,000 patients supporting the use of these drugs over and beyond those the FDA has approved under Emergency Use Authorization (EUA) statutes. Despite this, four years later, the FDA continues to fiercely deny ivermectin’s and HCQ’s efficacy and safety under proper administration. Why this blatant cover-up?

Every CDC effort to approve a novel drug treatment for SARS-CoV-2 infections has been a dismal failure. Aside from monoclonal antibody therapy, only three anti-Covid-19 drugs have been approved under an EUA in the United States. None met their promised expectations from either the manufacturer or our federal health agencies.  With their poor efficacy rates, safety profiles and a black box warning slapped upon Pfizer’s anti-Covid-19 drug Paxlovid, the CDC is scrambling to find new viable alternatives in the pharmaceutical pipeline. Bloomberg amplifies the fake Covid-19 treatment crisis by lamenting that repurposed drugs such as ivermectin are gaining global popularity as “the world needs effective Covid drugs.”[2]

Shortly after the pandemic was formally announced, the FDA recommended the cheap over the counter anti-malarial drug hydroxychloroquine but then quickly reversed its decision after Fauci publicly announced the future arrival of Gilead Sciences’ novel intravenous drug Remdesivir. The FDA’s and European Union’s approvals of Remdesivir baffled many scientists, according to the journal Science, who questioned its therapeutic value and kept a close watch on the drug’s clinical reports about a “disproportionally high number of reports of liver and kidney problems.”[3] Even an earlier Chinese study published in The Lancet found that remdesivir had no impact on the coronavirus. The Science article notes that the “FDA never consulted a group of outside experts that it has at the ready to weigh in on complicated antiviral drug issues.”[4] Six months before remdesivir received EUA approval, Anthony Fauci had already hailed the drug as a major breakthrough that would establish a new “standard of care” in Covid-19 treatment.[5]

Today, remdesivir is being increasingly recognized as a debacle in antiviral therapeutic care. Even the WHO released a “conditional recommendation against the use of remdesivir in hospitalized patients, regardless of disease severity, as there is currently no evidence that remdesivir improves survival and other outcomes in these patients.” An Italian study observed a 416 percent increase in hepatocellular injuries among hospitalized Covid-19 patients treated with Remdesivir.[6]  And a smaller Taiwanese study of hospitalized unvaccinated patients reported a 185 percent higher mortality during late remdesivir treatment.[7]

Earlier this year, Pfizer’s novel oral Covid-19 medication Paxlovid was given an FDA black box warning for clinically significant adverse reactions that can potentially be fatal. Because the company does not permit independent random-controlled trials to investigate its drug, other than retrospective studies, we only have Pfizer’s own data to rely upon. Nevertheless, The Lancet published a study by a team of Chinese scientists at Shanghai Jiao Tong School of Medicine that managed to look at Paxlovid’s use among critically ill patients hospitalized with Covid-19. The study reported a 27 percent higher risk of the infection progressing, a 67 percent increased risk in requiring ventilation, and 10 percent longer stays in ICU facilities.[8]

Paxlovid is a combination of a novel SARS-CoV-2 protease inhibitor and the HIV protease inhibitor ritonavir. The FDA approved Paxlovid under a EUA with the claim it was safe. However, on the government’s HIV.gov website for ritonavir it is clearly stated that the drug “can cause serious life-threatening side effects. These include inflammation of the pancreas (pancreatitis), heart rhythm problems, severe skin rash and allergic reactions, liver problems and drug interactions.”[9] Perhaps due to the drug’s serious side effects, it is no longer used solely against HIV, but rather is given in smaller doses as a booster for AZT-related drugs. Being highly toxic, ritonavir is also not recommended for pregnant women and has been shown to interfere with hormone-based birth control efficacy. 

Paxlovid only received FDA EUA approval in May 2023. At that time, the agency claimed there was no evidence that patients who were treated with the drug rebounded and came down with Covid. However, shortly thereafter this was determined to be untrue.[10] A Harvard analysis found that 21 percent of Paxlovid recipients will remain contagious and likely succumb to a viral rebound compared to only 1.8 percent who did not take the drug.

Merck’s anti-Covid-19 drug molnupiravir (Lagevrio) also has an FDA black box warning for potential fetal harm when administered to pregnant women. Why the drug was ever approved under an EUA seems to be an enigma. The drug’s antiviral activity is based upon a metabolite known as NHC, which for many years has been known to create havoc in an enzyme crucial for viral replication by inserting errors into the virus’ genetic code. The theory is: produce enough errors and the virus kills itself off. However, molnupiravir can cause hundreds of mutations thereby “supercharging” the manufacturing of new Covid-19 viral strains. Moreover, according to a Forbes article, the drug’s mutagenic powers may also interfere with our own body’s enzymes and DNA.[11] Another Forbes article points out that Merck’s clinical trial only enrolled around 1,500 participants, which is far too “small to pick up on rare mutagenic events.”[12]

Molnupiravir has a poor efficacy rate across the board including viral clearance, recovery, and hospitalizations/death (68 percent).[13] One trial, funded by Merck, concluded the drug had no clinical benefit.[14] More worrisome, the drug also has life-threatening adverse effects including mutagenic risks to human DNA and mitochondria, carcinogenic activity and embryonic death.[15]

Each of these drugs have been outrageous cash cows for their manufacturers. Remdesivir is priced at $3,120 per treatment and earned Gilead $5.6 billion in sales for 2021.

Pfizer’s Paxlovid is priced at $1,390 per treatment. Last year, the company’s revenues for its Covid products—Paxlovid and the Comirnaty vaccine—came in at $12.5 billion, and, according to Fierce Pharma, Pfizer wrote off an additional $4.7 billion on its overstocked Paxlovid inventory.[16] Merck’s molnupiravir’s sales for 2022 cashed in almost $5.7 billion. Despite their profits, none of these drugs have been shown convincingly to have measurably lessened the pandemic nor the spread of SARS-CoV-2. 

Despite all the attention and medical hype about novel experimental antiviral drugs to treat Covid-19, Anthony Fauci and other federal officials had full knowledge that other FDA-approved drugs existed that could have been quickly repurposed at minimal expense to effectively treat Covid-19 infections. Repurposing existing drugs to treat illness is a common occurrence. The antiparasitic and antiviral drug Ivermectin best stands out. Its effectiveness was observed to be so remarkable and multifaceted that researchers started to investigate its potential.  

The mainstream media, including many liberal news sources who pride themselves on their independence, continue to channel the voices of Anthony Fauci, the CDC and FDA to demonize ivermectin and other generic drugs for treating Covid-19 and to reduce hospitalization and deaths. This propaganda campaign, however, has completely ignored the large body of medical literature that shows ivermectin’s statistically significant efficacy against symptomatic and asymptomatic SARS-2 infections.

Originally developed for veterinarian use, in 1987, the FDA approved ivermectin for treating two parasitic diseases, river blindness and stronglyoidiasis, in humans. Since then an enormous body of medical research has grown showing ivermectin’s effectiveness for treating other diseases. Its broad range of antiviral properties has shown efficacy against many RNA viruses such avian influenza, zika, dengue, HIV, West Nile, yellow fever, chikungunya and earlier severe respiratory coronaviruses. It has also been shown to be effective against DNA viruses such as herpes, polyomavirus, and circovirus-2.[17]

Unsurprisingly, ivermectin’s inventors Drs. William Campbell and Satoshi Omura were awarded the 2015 Nobel Prize in Physiology and Medicine.

It has been prescribed to hundreds of millions of people worldwide. Given its decades’ long record of in vitro efficacy, it should have been self-evident for Fauci’s NIAID, the CDC and the WHO to rapidly conduct in vivo trials to usher ivermectin as a first line of defense for early stage Covid-19 infections and for use as a safe prophylaxis.

For example, if funding were devoted for the rapid development of a micro-based pulmonary delivery system, mortality rates would have been miniscule and the pandemic would have been lessened greatly.[18] Repurposing ivermectin could have been achieved very quickly at a minor expense.[19] However, despite all the medical evidence confirming ivermectin’s strong antiviral properties and its impeccable safety record when administered properly, we instead witnessed a sophisticated government-orchestrated campaign to declare war against ivermectin and another antiviral drug, hydroxychloroquine (HCQ), in favor of far more expensive and EUA approved experimental drugs. Unlike the US, other nations were eager to find older drugs to repurpose against Covid-19 and protect their populations. A Johns Hopkins University analysis offered the theory that a reason why many African countries had very few to near zero Covid-19 fatalities was because of widespread deployment of ivermectin. In February 2020, the National Health Commission of China, for example, was the first to include hydroxychloroquine in its guidelines for treating mild, moderate and severe SARS-2 cases. Eight Latin American nations distribute home Covid-19 treatment kits that include ivermectin.[20] Why did the US and most European countries swayed by the US and the WHO fail to follow suit?

Early in the pandemic, physicians in other nations where treatment was less restricted, such as Spain and Italy, shared data with American physicians about effective treatments against the SARS-2 virus. In addition, there was a large corpus of medical research indicating that older antiviral drugs could be repurposed. Doctors who started to prescribe drugs such as ivermectin and HCQ, along with Vitamin D and zinc supplementation, observed remarkable results. Unlike the dismal recovery and high mortality rates reported in hospitals and large clinics that relied upon strict isolation, quarantine, and ventilator interventions, this small fringe group of physicians reported very few deaths among their large patient loads. Even reported deaths were more often than not compounded by patients’ comorbidities, poor medical facilities and other anomalies. 

Very early into the pandemic, medical papers indicated ivermectin was a highly effective drug to treat SARS-2 infections.

In April 2020, less than a month after the WHO declared Covid-19 as a global pandemic, Australian researchers at the Peter Doherty Institute of Infection and Immunity published a paper demonstrating that a single ivermectin dose can control SARS-CoV-2 viral replication within 24-48 hours.[21] Monash University’s Biomedicine Discovery Institute in Australia had also published an early study that ivermectin destroyed SARS-2 infected cell cultures by 99.8 percent within 48 hours. But no American federal health official paid any attention.

As of March 2024, a database for all studies and trials investigating ivermectin against Covid-19 infections records a total of 248 studies, 195 peer-reviewed, and 102 involving controlled groups reporting an average 61 percent improvement for early infections, a 39 percent success rate in treating late infections, and an 85 percent average success rate for use as a preventative prophylaxis.[22] Moreover, prescribing ivermectin reduced mortality by 49 percent, compared to remdesivir’s 4 percent, Pfizer’s Paxlovid’s 31 percent, and molnupiravir’s 22 percent. Even hydroxychloroquine well outperforms these drugs mortality risk for early treatment at 66 percent. 

A noteworthy study conducted in Brazil and published in the Cureus Journal of Medical Science prescribed ivermectin in a citywide prophylaxis program in a town of 223,000 residents. 133,000 took ivermectin. The results for a population of this size are indisputable in concluding that ivermectin is a safe first line of defense to confront the pandemic. Covid mortality was reduced 90 percent. There was also a 67 percent lower risk of hospitalization and a 44 percent decrease in Covid cases. Garcia-Aquilar et al reports a Mexican in vitro analysis showing a definitive interaction between ivermectin and the SAR-CoV-2 spike protein, which would account for its high efficacy in Covid-19 cases.[23]

The All India Institute for Medical Science (AIIMS) and the Indian Council of Medical Research (ICMR), two of India’s most prestigious institutions, acted against the WHO and launched an ivermectin treatment campaign in several states. In Uttar Pradesh there was a 95 percent decrease in morality (a decline from 37,944 to 2,014). The Indian capital of New Delhi witnessed a 97 percent reduction. During the same time period, the state of Tamil Nadu, which followed the WHO’s ban on ivermectin, had a 173 percent increase in deaths (from 10,986 to 30,016 deaths).

There have been many concerted efforts to discredit ivermectin and other repurposed drugs’ effectiveness. Most notable is the large TOGETHER Trial Brazil study published in the New England Journal of Medicine (NEJM) that concluded both ivermectin and another repurposed drug fluvoxamine showed no beneficial signs for treating Covid-19 patients. The study was widely reported in the mainstream media. However, a Cato Institute analysis discovered the study in fact showed its benefits and the results were in agreement with 87 percent of other clinical trials investigating ivermectin. The Cato analysis identifies many odd anomalies in how the trial was conducted including an unspecified placebo—although it is suspected it was Vitamin C, which has itself been shown to be mildly effective against the SARS-CoV-2 virus, and protocol changes as the study was underway including inclusion/exclusion criteria. By his own admission the TOGETHER Trial’s principal investigator Dr. Ed Mills at McMaster University in Ontario “designs clinical trials, predominantly for the Bill and Melinda Gates Foundation.”[24] In a McMaster University press release, the Gates foundation is listed as a funder for the study to debunk ivermectin and fluvoxamine.[25] Oddly, Gates is nowhere listed among the several funders in the NEJM study’s disclosure. In addition, TOGETHER Trials is owned by the Canadian for profit startup Purpose Life Sciences, founded by Mills; legal documents showed Mills’ PLS is largely funded and controlled by Sam Bankman Fried’s FTX who invested $53 million into the project. Administrators of FTX’s bankruptcy are suing PLS for fraud.[26]

In short, the ivermectin/fluvoxamine TOGETHER Trial was a complete medical sham and intentionally designed for one single purpose: to fuel media disinformation in order to undermine ivermectin’s superior efficacy and safety profile to Big Pharma’s more profitable designer drugs. 

In 2004, the US Congress passed an amendment to the Federal Food, Drug and Cosmetic Act known as Emergency Use Authorization (EUA). This piece of legislature legalized an anti-regulatory pathway to allow experimental medical interventions to be expedited and bypass standard FDA safety evaluations in the event of bioterrorist threats and national health emergencies such as pandemics. At the time, passage of the EUA amendment made sense because it was partially in response to the 2001 anthrax attacks and the US’s entry into an age of international terrorism. However, the amendment raises some serious considerations. Before the Covid-19 pandemic, EUAs had only been authorized on four occasions: the 2005 avian H5N1 and 2009 H1N1 swine flu threats, the 2014 Ebola and the 2016 Zikra viruses. Each of these pathogen scares proved to be false alarms that posed no threat of pandemic proportions to Americans. The fifth time EUAs were invoked was in 2020 during the Covid-19 pandemic, which at the time seemed far more plausible. 

Before the government can authorize an EUA to deploy an experimental diagnostic product, drug or vaccine, certain requirements must be fulfilled. First, the Secretary of the Department of Health and Human Services (HHS) must have sufficient proof that the nation is being confronted with a serious life-threatening health emergency. Second, the drug(s) and/or vaccine(s) under consideration must have sufficient scientific evidence to suggest they will likely be effective against the medical threat. The evidence must at least include preclinical and observational data showing the product targets the organism, disease or condition. Third, although the drug or vaccine does not undergo a rigorous evaluation, it must at least show that its potential and known benefits outweigh its potential and known risks. In addition, the product must be manufactured in complete accordance with standard quality control and safety assurances. 

When we look back at the government’s many debacles during the Covid-19 pandemic, other EUA requirements warrant the spotlight. On the one hand, an EUA cannot be authorized for any product or intervention if there is an FDA alternative approved product already available, unless the experimental product is clearly proven to have a significant advantage. Moreover, and perhaps more important, EUAs demand informed consent. Every individual who receives the drug or vaccine must be thoroughly informed about its experimental status and its potential risks and benefits. Recipients must also be properly informed about the alternatives to the experimental product and nobody should be forced to take it.

Finally, an EUA requires robust safety monitoring and reporting of adverse events, injuries and deaths potentially due to the drug or vaccine. This is the responsibility not only of the private pharmaceutical manufacturers but also the FDA, physicians, hospitals, clinics and other healthcare professionals. 

Obviously important cautions must be considered after approving a medical intervention under the EUA requirements. Foremost are the inherent health risks of any rapid response of experimental medical interventions, especially novel drugs and vaccines. As we observed during the FDA approval process and roll out of Pfizer’s and Moderna’s mRNA Covid-19 jabs, no long-term human trials were conducted to even estimate a reliable baseline of their relative efficacy and safety. The American public has blindly placed its trust in our federal health authorities decision-making. It is expected that under a national health emergency, the authorities would be completely transparent and act only by the highest ethical standards. However our institutions betrayed public trust and either ignored or transgressed cautions underlying EUA approved medical interventions in every conceivable way. Moreover, conflicts of interests have been discovered to have plagued the entire EUA review process.  

Although the EUA amendment provides some protections to authorized drug and vaccine manufacturers, it was the Public Readiness and Emergency Preparedness Act (PREP) in 2005 that expanded liability protections. In addition to protecting private corporations, PREP also shields company executives and employees from claims of personal injury or death resulting from the administration of authorized countermeasures. The only exceptions for liability are if the company or its executive offices are proven to have engaged in intentional and/or criminal misconduct with conscious disregard for the rights and safety of those taking their drugs and vaccines. 

During the pandemic, the FDA issued widespread EUAs with liability immunity for the PCR diagnostic kits for SARS-2, the mRNA vaccines and the anti-Covid-19 drugs. Curiously, the Secretary of the Department of Health and Human Services invoked the PREP Act on February 4, 2020 giving liability protections; this was over a month before the pandemic was officially announced, which raises serious questions about prior-planning before the viral outbreak in Wuhan, China. 

From the pandemic’s outset, Fauci embarked on the media circuit to promise Americans that federal health agencies were doing everything within their means to get a vaccine on the market because there was no available drug to clear the SARS-2 virus. As we have seen with respect to ivermectin alone, this was patently false. Rather the government placed an overriding emphasis on vaccination with a near total disregard for implementing very simple preventative measures to inhibit viral progression. Once mass vaccinations were underway, we were promised that the SARS-2 virus would be defeated and life would return to normal. In retrospect, we can look back and state with a degree of certainty that American health authorities and these products’ corporate manufacturers may have violated almost every EUA requirement. Everything that went wrong with the PCR kits, the experimental mRNA vaccines and novel drugs could have been avoided if the government had diligently repurposed effective and safe measures as pandemic countermeasures. Very likely, hundreds of thousands of lives, perhaps millions, would have been saved. 

Similarly the FDA issued a warning statement against the use of ivermectin. Even ivermectin’s manufacturer Merck discredited its own product. Shortly after ridiculing its drug, the Alliance for Natural Health reported, “Merck announced positive results from a clinical trial on a new drug called molnupiravir in eliminating the virus in infected patients.”[27]

And still the FDA considers these novel patented drugs to be superior to ivermectin. Favoring a vaccine regime and government-controlled surveillance measures to track every American’s movements, American health officials blatantly neglected their own pandemic policies’ severe health consequences. Ineffective lockdowns, masks, social isolation, unsound critical care interventions such as relying upon ventilators, and the sole EUA approvals of the costly and insufficiently effective drugs brought about nightmares for tens of millions of adults and children. This was all undertaken under Fauci’s watch and the heads of the US health agencies in direct violation of the EUA requirements to only authorize drugs and medical interventions when no other safe and effective alternative is available. Alternatives were available.

The 4-year history of the pandemic highlights a sharp distinction between dependable medical research and pseudoscientific fraud. The CDC adopted a common Soviet era practice to redefine the very definition of a vaccine and the parameters of vaccine efficacy in order to fit economic and ideological agendas. This explains Washington’s aggressive public relations endeavors to silence medical opponents. According to cardiologist Dr. Michael Goodkin’s private investigations, several of the most cited studies discrediting ivermectin’s antiviral benefits were intentionally manipulated in order to produce “fake” results.[28] These studies were then widely distributed to the AMA, American College of Physicians and across mainstream media to author “hit pieces” to demonize ivermectin and other repurposed drugs. The government’s belligerent and reactive diatribes, brazenly or casually advocating for censorship, were direct violations of scientific and medical integrity and contributed nothing towards developing constructive policies for handling a pandemic with a minimal cost to life. The consequence has been a less informed and grossly naïve public, which was gaslighted into believing lies. 

The FDA’s EUAs for the Covid-19 vaccines and novel experimental drugs were in fact an attack on the amendments and PREP directives. Neither the vaccines nor drugs warranted emergency authorization because effective and safe alternatives were readily available. No doubt a Congressional investigation would uncover criminal misconduct and conscious fraud. Moreover, these violations of the PREP Act may have the potential to lead directly into medical crimes against humanity as outlined in the Nuremberg Code.

Although the Nuremberg Code has not been officially adopted in its entirety as law by any nation or major medical association, other international treaties, such as the Universal Declaration of Human Rights, the World Medical Association Declaration of Helsinki (which is not legally binding), the International Covenant on Civil and Political Rights (ICCPR) and the International Ethical Guidelines for Biomedical Research on Human Subjects incorporate some of Nuremberg’s main principles that aim to protect people from unethical and forced medical research. Although the US signed the ICCPR as an intentional party, the US Senate never ratified it. The ICCPR’s Article 7 clearly states, “No one shall be subject to torture or cruel, inhuman or degrading treatment or punishment,” which can legally be interpreted to include forced medical experimentation implied as cruel, inhuman treatment. Other ICCPR articles, 6 and 17, are also applicable to medical experimentation to ensure ethical conduct, obtaining proper informed consent and the right to life and privacy. For a moment, consider the numerous senior citizens in nursing homes and hospitals who were simply administered experimental Covid-19 vaccines without full knowledge about what they were receiving. And now how many children are being coerced by the pseudoscience of health officials’ lies to be vaccinated without any knowledge of these mRNA products’ risk-benefit ratio?

The US is also a signatory to the Helsinki Declaration, which, although not directly aligned with Nuremberg, shares much in common. The Declaration shares some common features with the EUA amendment and PREP Act. These include voluntary informed consent—which is universally accepted, adequate risk and benefit information about medical interventions, and an emphasis on the principle of medical beneficence (promoting well-being and the Hippocratic rule of doing no harm). It also guarantees protections for vulnerable groups, especially pregnant women and children, which the US government and vaccine makers directly violated by conducting trials on these groups with full knowledge about these vaccines’ adverse events in adults. In addition, weighing the scientific evidence to assess the risk-benefit ratios between prescribing ivermectin and HCQ over the new generation of novel experimental drugs conclusively favors the former. This alone directly violates the ethical medical principles noted above. 

However, the failure to repurpose life-saving drugs is less criminal than the questionable unethical motivations to usher a new generation of genetically engineered vaccines that have never before been adequately researched in human trials for long term safety. This mass experimentation, which continues to threaten the health and well-being of millions of people, is global and can legally be interpreted as a genocidal attack on humanity.

If the emerging data for increasing injuries and deaths due to the Covid-19 vaccines is reliable—and we believe it is—the handling of the pandemic can be regarded as the largest medical crime in human history. In time, and with shifting political allegiances and public demands to hold our leaders in government and private industry accountable, the architects of this medical war against civilization will be brought to justice. 

*

Richard Gale is the Executive Producer of the Progressive Radio Network and a former Senior Research Analyst in the biotechnology and genomic industries.

Dr. Gary Null is host of the nation’s longest running public radio program on alternative and nutritional health and a multi-award-winning documentary film director, including his recent Last Call to Tomorrow.

Notes

[1] https://www.cnn.com/videos/health/2021/08/29/dr-anthony-fauci-ivermectin-covid-19-sotu-vpx.cnn

[2] https://www.bloomberg.com/news/newsletters/2023-01-24/the-world-needs-effective-covid-drugs-as-ivermectin-persists

[3] https://www.sciencemag.org/news/2020/10/very-very-bad-look-remdesivir-first-fda-approved-covid-19-drug

[4] https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(20)31022-9/fulltext

[5] https://www.cnbc.com/2020/04/29/dr-anthony-fauci-says-data-from-remdesivir-coronavirus-drug-trial-shows-quite-good-news.html

[6] https://www.dldjournalonline.com/article/S1590-8658(21)00923-3/fulltext

[7] https://journals.lww.com/md-journal/fulltext/2023/12290/the_association_between_covid_19_vaccination_and.45.aspx

[8] https://www.thelancet.com/action/showPdf?pii=S2666-6065%25252823%25252900012-3

[9] https://clinicalinfo.hiv.gov/en/drugs/ritonavir/patient

[10] https://www.yalemedicine.org/news/13-things-to-know-paxlovid-covid-19

[11] https://www.forbes.com/sites/williamhaseltine/2021/11/01/supercharging-new-viral-variants-the-dangers-of-molnupiravir-part-1/

[12] https://www.forbes.com/sites/williamhaseltine/2021/11/02/harming-those-who-receive-it-the-dangers-of-molnupiravir-part-2

[13] https://www.medrxiv.org/content/10.1101/2023.01.20.23284849v1.full.pdf

[14] https://evidence.nejm.org/doi/pdf/10.1056/EVIDoa2100044

[15] https://c19early.org/waters.html

[16] https://www.fiercepharma.com/pharma/pfizer-gets-walloped-56b-write-down-covid-sales-continue-disappoint

[17] https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7290143/

[18] https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7539925/

[19] https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7564151/

[20] https://www.bu.edu/sph/news/articles/2023/8-latin-american-governments-distributed-ivermectin-sans-evidence-to-treat-covid

[21] https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7129059/

[22] https://c19ivermectin.com

[23] https://www.mdpi.com/1422-0067/24/22/16392

[24] https://empendium.com/mcmtextbook/interviews/perspective/236226,covid-19-to-treat-or-not-to-treat-platform-trials

[25] https://www.eurekalert.org/news-releases/855535

[26] https://c19ivm.org/tallaksen.html

[27] https://anh-usa.org/fda-ensures-pharma-profits-on-covid/

[28] https://www.trialsitenews.com/a/are-major-ivermectin-studies-designed-for-failure

April 6, 2024 Posted by | Corruption, Deception, Full Spectrum Dominance, Science and Pseudo-Science, Timeless or most popular, War Crimes | , , , , , , | Leave a comment

New Studies: Pfizer’s Paxlovid doesn’t actually work, ‘rebound’ symptoms occur 25x more often than advertised

Failed drug cost U.S. taxpayers $12.6 billion

By Jordan Schachtel | The Dossier | April 5, 2024

Pfizer first scammed the world with its “100% safe and effective” Covid mRNA vaccines, and as it turns out, that was just the opening salvo from a pharmaceutical cartel that is inundated with corruption and deceit.

I wanted to turn your attention to two significant recent studies on Paxlovid, the Covid-19 oral pill that the U.S. government spent $12.6 billion taxpayer dollars on subsidizing for Pfizer.

The first study, which is brought to you by Pfizer funds (though they noticeably don’t use the brand name Paxlovid in the study), finds that Paxlovid does not actually work. They’ve known this since July, 2022, but for reasons unknown, waited two years to publish the results.

“The time to sustained alleviation of all signs and symptoms of Covid-19 did not differ significantly between participants who received nirmatrelvir–ritonavir (Paxlovid) and those who received placebo,” the authors write in this New England Journal of Medicine study, which was published on April 3rd.

That’s right. It doesn’t work at all.

In rolling out Paxlovid, Pfizer claimed in a press release that its preliminary data showed an 89% reduction in hospitalization and death for patients who took the pill.

Curiously, the Pfizer-funded study concluded in July 2022, just months after Paxlovid became available, but this seems to be the first time that results have been public.

Now, hundreds of millions of manufactured doses later, the most sophisticated apples to apples comparison shows that it isn’t effective whatsoever.

But it gets worse.

Remember “Paxlovid rebound”?

That’s short for people’s symptoms coming back after taking a course of Paxlovid.

When Paxlovid first hit pharmacy shelves, Pfizer claimed that Paxlovid rebound was inconsequential, amounting to 1 or 2 percent of patients who were prescribed the drug.

But a late March study published in The Journal of the American Medical Association (JAMA) found that about 1 in 4 patients on Paxlovid suffered from “Paxlovid rebound.” This study didn’t just analyze the presence of viral fragments. It found that 24.5 percent of enrolled patients on Paxlovid suffered from *symptomatic* rebound.

Now it makes sense why so many high profile figures, such as Joe Biden and Anthony Fauci, had bouts of “Paxlovid rebound.” It isn’t rare whatsoever.

Now imagine if Pfizer told the truth about its failed Covid-19 drug from the beginning. That truth would’ve resulted in Pfizer taking a massive financial hit, given that they relied on Paxlovid to sustain their multi billion dollar profit margins.

Meanwhile, Pfizer’s market value has continued to crash over the past year. Fewer and fewer people are buying what Pfizer is selling.

Now who will be held accountable for the greatest pharmaceutical fraud and swindle operation of all time?

April 6, 2024 Posted by | Deception, Science and Pseudo-Science | 1 Comment

Disinformation “Expert” Tells People To Only Use “Trusted Sources,” Avoid “Doing Your Own Research”

By Cindy Harper | Reclaim The Net | April 6, 2024

Brianna Lyman, elections correspondent at The Federalist, recently reported on a panel discussion featuring Al Schmidt, Pennsylvania Secretary of the Commonwealth, and Beth Schwanke, Executive Director of the Pitt Disinformation Lab. Schmidt and Schwanke, speaking at a forum organized by Spotlight PA, voiced their stance on “misinformation” and “disinformation” surrounding elections. Strikingly, Schwanke recommended that rather than conducting self-led investigations, Pennsylvanians should place their confidence in so-called “trusted” sources. These include certain institutions and media outlets that have unfortunately been tied in the past to acts of censorship.

“One thing everyone can do to make sure they are seeing accurate information is to use trusted sources. So in elections that means using the Department of State, that means using your county elections office, it means using media organizations that follow, that adhere, to professional journalism standards like … your local NPR affiliate,” Schwanke said. “And it doesn’t mean you know, ‘doing your own research’ and just asking questions and sharing, you know, posts from – I don’t know, in my case, it’s Uncle Joe, right? It means being thoughtful about where your sources are coming from.”

Schwanke’s advice, interestingly, seemed to discourage individual research, questioning, and sharing of ideas. Instead, she advocated the use of sources like the Department of State, county elections offices, and, strikingly, media organizations such as local NPR affiliates, which she implied upheld superior journalistic standards.

Despite what Schwanke says, the importance of being vigilant about our sources of information cannot be overstated. This was vividly demonstrated in the lead-up to the 2020 election when a significant story on Hunter Biden’s laptop by the New York Post was unjustly labeled “disinformation,” and subsequently suppressed across several tech platforms.

As The Federalist reported, what made matters worse, in an incident hinting at bias, NPR blatantly refused to report on the story, with its Managing Editor Terence Samuels declaring it as unworthy of coverage.

The Pennsylvania State Department presented a similar cause for alarm. It announced its collaboration with the Cybersecurity and Infrastructure Security Agency (CISA) to monitor and control online talks deemed a “threat” related to the election process. Despite its claimed intention to offer voters accurate, trustworthy election-related data and to counter threats such as so-called “misinformation,” there is good reason to question the impartiality of its activities. Case in point, CISA had previously facilitated the silencing of Americans expressing valid concerns on social media, as if they were spreading “disinformation,” and even had a post from President Donald Trump flagged under these pretenses.

Related: 

Pennsylvania Collaborates With DHS and CISA To Monitor Online Election-Related Speech

April 6, 2024 Posted by | Civil Liberties, Deception, Fake News, Full Spectrum Dominance, Mainstream Media, Warmongering | , | Leave a comment

New Challenges to the First Amendment from the Biden Administration

By Peter van Buren | We Meant Well | April 3, 2024

The great irony is despite all the fear mongering spewed out about Donald Trump ending democracy, it is mostly the Democrats who are taking shots at its most sacred freedoms, those of the First Amendment.

The House recently passed a bill, HR 7521, seeking to “ban” the popular app Tik Tok from America’s smartphones. The logic works like this: Tik Tok is owned by a Chinese company. Chinese companies are under the control of the Chinese Communists. Therefore, Tik Tok is brainwashing American youth while at the same time gathering their personal data for some undefined yet assumed nefarious use. Tik Tok thus should be banned.

No evidence has been presented for any of the assertions listed — no evidence the Chinese government exerts control over Tik Tok, whose contents are 100 percent user-created, no evidence the app has any purpose other than to make money, and no evidence the app collects data and uses it in some way, nefarious or not. It just feels scary bad, like any other Red Scare, and so the House moved to ban it. The Senate votes soon, and Joe Biden says he will sign the bill if it reaches him.

This is not the first time the government has tried to ban Tik Tok. In 2021, President Donald Trump issued an executive order against Tik Tok that was halted in federal court when a judge found it was “arbitrary and capricious.” Another judge found that the national security threat posted by Tik Tok was “phrased in the hypothetical.” When the state of Montana tried to ban the app in 2023, a federal judge found it “oversteps state power and infringes on the constitutional rights of users,” with a “pervasive undertone of anti-Chinese sentiment.” Candidate Trump now opposes the Tik Tok ban.

You’d think that was enough for Tik Tok. Yet note the ban is just on some Chinese company owning the app and the bill allows for an American company or ally to buy Tik Tok and go on its merry way. It’s not a ban, it’s a hijacking. And don’t think the Chinese won’t find an American app to retaliate against. Listening Apple and Android?

But that is not where the true First Amendment challenge lies, though “banning” the app can itself be seen as restricting speech. The real challenge lies in the details of the actual bill, another Patriot Act in hiding.

Section 2(a)(1) of the bill prohibits “foreign adversary controlled applications” (FACA) from operating in the U.S. The prohibition applies not just to the app itself but to app stores and Internet hosting providers. There’s even a provision for a penalty of $5,000 per user fine; Tik Tok has 170 million users. Effectively, the bill creates a Federal government kill switch preventing distribution of “prohibited” apps or websites at the hosting level, clear top-down central government censorship of speech and absolutely unconstitutional under the First Amendment. Unless of course the weasel excuse is used that the actual killing of the imported app is carried out by Apple and Google as proxies without being touched by the Feds, the same trick currently used to gather American citizen data, in addition to direct hoovering up of material by the NSA on a scale the Chinese could only dream of.

What is a “foreign adversary controlled application” under Section 2(g)(3) of the new bill? Any social/content-sharing website, desktop app, mobile app, or VR app that has more than a million monthly active users creating content is a FACA when two conditions are met: First, if it is “controlled by a foreign adversary” or a subsidiary of or a successor to an entity controlled by a foreign adversary. Second, if the President determines it “presents a significant threat to the national security of the United States.” The term “controlled by a foreign adversary” means that the company (a) is domiciled in, headquartered in, or organized under the laws of a foreign adversary country; or (b) has a 20 percent ownership group from one of those countries; or (c) is “subject to the direction or control of a foreign person or entity” from one of those countries (Section 2(g)(1). “Adversary” is currently defined elsewhere in the U.S. Code as Russia, China, North Korea or Iran, but can be changed to someday be, say, France (remember “Freedom Fries“?)

There in the details lies the real challenge to the First Amendment, a set of vague criteria that allow the president to ban websites and apps based on his own finding of threat. No appeals, no due process. Censorship.

Americans have a right to speak freely, and to listen/read/watch freely and make up their own minds. The Supreme Court in Lamont v. Postmaster General already ruled in 1964 that this right even extends to foreign propaganda (the case involved Soviet propaganda materials passing through the U.S. Mail.) In addition, the irony of the U.S. government showing concern for what a foreign company might do with user data when in the U.S. such data is openly for sale, including to the government itself, cannot be dismissed. The Tik Tok ban is bad law, likely unconstitutional, and generally unconscionable.

The Tik Tok bill is not the only current challenge to the First Amendment. As exposed by the Twitter Files and elsewhere, for years the Biden administration worked hand-in-glove with the big tech social media companies, @jack’s old Twitter in particular, to censor speech. Various agencies, including those responsible for Covid-19 policy, would contact the media companies to demand wrongthink posts be taken down. Particularly offensive were conservative posts questioning the efficiency and safety of the Covid vaccine, and those dealing with election fraud.

The question of whether or not the government can do that — demanding specific online speech be killed — reached the Supreme Court, and oral arguments were held earlier this month in the case of Murthy v. Missouri. The Court seemed skeptical of the idea that such action by the government was unconstitutional on its face, as the states claimed. Instead, the justices’ questions seemed to lean toward how the censorship was done. The government was free to persuade social media carriers, cajole them, argue with them but as long as the government did not force them to take something down, it was likely legal. The states contend the looming power of the federal government made each request, however bland and polite, into a threat. Same as when the mafia thug in the movies says “Nice home you have here, hate to see anything happen to it if you’re late paying us.” In one interaction a government watchdog seeking to deep six some posts stated “the White House is considering its options” if the take down effort fails.

There was room for debate. Justice Alito stated “When I see the White House and Federal officials repeatedly saying that Facebook and the Federal government should be partners… regular meetings, constant pestering… Wow, I cannot imagine Federal officials taking that approach to print media.” Alito also thought the barrage of emails from the White House and others to the social media companies may have met the legal standard for coercion. The states agreed, saying “Pressuring platforms in back rooms, shielded from public view, is not using a bully pulpit. That’s just being a bully… We don’t need coercion as a theory. The government ‘cannot induce, encourage or promote’ to get private actors to do what government cannot: censor Americans’ speech.”

Justice Kentaji Brown Jackson came back with “Whether or not the government can do this… depends on the application of our First Amendment jurisprudence. There may be circumstances in which the government could prohibit certain speech on the internet or otherwise. My biggest concern is that your view has the First Amendment hamstringing the government in significant ways.”

Justice Barrett seemed uncomfortable with the lower courts’ conclusion that the Biden administration could be banned not only from “coercion,” but also from any action that “significantly encourages” platforms to take down protected speech. “Encouragement would sweep in an awful lot,” she said.

Interactions between administration officials and news outlets are part of a valuable dialogue that is not prohibited by the First Amendment, said Justices Kavanaugh and Kagan. The Justices suggested instead there is a role for vigorous efforts by the government to combat bad speech, for example discouraging posts harmful to children or conveying anti-Semitic or Islamophobic messages.

Brown’s, et al, remarks are frightening from a constitutional point of view, basically saying when the government is ineffective in creating dominant content of its own to address public messaging (i.e., “Vaccines are safe”) it justifies proxy censorship to eliminate counter information.

A Supreme Court decision is expected in June.

April 6, 2024 Posted by | Civil Liberties, Full Spectrum Dominance | , | Leave a comment

Mexico warns Israel for ‘protecting’ suspect in disappearance of 43 students

Press TV – April 6, 2024

Mexico has warned that if Israel continues with its refusal to extradite a fugitive security official wanted in connection with the disappearance of 43 Mexican college students a decade ago, their bilateral ties may be damaged.

Back in September 2014, 43 male students disappeared from the Ayotzinapa Rural Teachers’ College after being abducted in Iguala, in the southwestern state of Guerrero. The students were traveling to a demonstration in Mexico City amid a drug war.

The official narrative by the government said at the time that corrupt police handed the ill-fated students over to drug gang henchmen, who then incinerated the students at a garbage dump and threw the ashes in the San Juan River.

Questioning the official narrative by some experts as well as growing anger in Mexico at federal inaction prompted the current administration, led by President Andres Manuel Lopez Obrador, to pledge to re-open the case.

Tomas Zeron, who headed the Criminal Investigation Agency that led the inquiry into the case – dubbed one of Mexico’s worst human rights tragedies – is wanted by the Mexican justice system for the crimes of torture, violation of human rights and forced disappearance of the 43 students.

“The lack of progress in resolving this case is interpreted as de facto protection by Israel of Tomas Zeron and threatens to become an irritating and disruptive factor with” Tel Aviv, the Mexican foreign ministry said in a statement on Friday.

The former official, who fled to Israel in 2020, has also been charged with the abuse of power and authority, embezzlement, fraud and criminal association. He has consistently denied all allegations.

Although Mexico and Israel do not have an extradition treaty, Mexico City has repeatedly asked Tel Aviv to hand over Zeron over allegations of serious irregularities in the probe into the said case, but all to no avail.

Zeron is one of the architects of the 2015 official narrative or the so-called “historical truth” regarding the fate of the disappeared students, whose exact circumstances of their disappearance are still unknown.

The victims’ families have so far strongly rejected that narrative.

April 6, 2024 Posted by | Full Spectrum Dominance | , , | Leave a comment

Israel takes dangerous step in the conflict by attacking Iranian diplomats

By Lucas Leiroz | Strategic Culture Foundation | April 5, 2024

Attacking embassies, consulates and diplomatic personnel is an intolerable crime under international law. The inviolability of diplomatic buildings is a global principle that enables the elementary conditions necessary for international relations. Even in situations of total war and high-intensity conflicts, respect for diplomacy must be observed by the belligerent sides to prevent even worse escalations of violence from occurring.

Israel, however, appears unwilling to respect any international norm. Recently, the Zionist State bombed an Iranian diplomatic building, close to the Iranian Embassy in Damascus. At least seven Iranian citizens were murdered in the operation, including diplomats and a senior Revolutionary Guard commander. As expected, Tehran has promised retaliation and is already mobilizing its military forces for a possible conflict situation.

In fact, the act of bombing diplomatic installations can be considered terrorism, as it deliberately aims to kill civilians, without any military objective. As we know, attacks against civilians have become increasingly frequent in the Zionist war strategy. The Israeli regime simply appears to see all Palestinians in the Gaza Strip as legitimate targets, which leads the IDF to destroy all of the city’s civilian infrastructure and generate an ever-increasing number of non-military casualties among local residents.

However, it appears that Israel is also expanding its attacks on civilian targets to the international level. The destruction of one of the buildings of the Iranian Embassy in Damascus was certainly one of the most serious moves ever made in the current conflict. To make matters worse, Israeli officials have promised to carry out more attacks against Iranian and Shiite public figures, regardless of where they are located. Apparently, from now on Tel Aviv will openly adopt a rhetoric of “hunting” against Iranians.

Obviously, this situation will only generate more escalations. Israel is accustomed to attacking targets with little power to react, such as the stateless Palestinians or Syria, which is recovering from a brutal civil war. Iran, however, is a country in a different position. Tehran is the largest military power in the Middle East, having impressive weapons production and combat mobilization capabilities. The country controls the production of the main current military equipment, with modern long-range missiles and drones among its main tools of war.

Furthermore, Iran has more than only its military and Revolutionary Guard, controlling a complex network of anti-Zionist movements across the Middle East – the so-called “Axis of Resistance”. Armed organizations such as Hezbollah, the Iraqi Resistance, Syrian Shiite militias, the Houthis and the Palestinian guerrillas themselves are members of the Axis and are willing to fight a war in favor of Iran at any time. Even if Israel strives to destroy targets linked to regular Iranian forces, it will be difficult to neutralize the top leaders of all these organizations at the same time.

An open war between Iran and Israel would be catastrophic for the region from all points of view. Analyzing the military power of both countries, it is possible to say that Israel is militarily weaker. However, Tel Aviv has nuclear weapons. The possibility that Iran also has such weapons cannot be ruled out, but at least publicly there is no information to prove this. What is known, however, is that the Iranians already have full uranium enrichment capacity and control the industrial process that could lead to the production of an atomic bomb.

In a war scenario, Iran would also be favored by its complex geography. As a large country and with mountains that protect some of its important cities and industrial centers, Iran is less vulnerable to collapse in the face of foreign incursions than Israel. Furthermore, Tehran would mobilize the Axis of Resistance militias to attack Israel on several flanks, quickly making the Zionist state unable to fight given the existence of multiple fronts. In this scenario, Israel would be forced to choose between two fates: surrender or the use of its extreme arsenal.

However, history shows us that Iran has a great capacity to achieve military objectives without generating collateral damage. The country is used to asymmetric warfare, responding with patience and high precision to the provocations suffered, without escalating the regional situation into total war. Tehran will certainly do its best to retaliate against Israel without a formal declaration of war. It is possible that there will be more Axis of Resistance attacks against occupation forces in the coming days, just as it is possible that Israeli and American targets will be destroyed in high-precision raids.

It is not yet certain that there will be an open war, but it is absolutely clear that there will be a serious escalation. Israel is making a serious mistake by thinking that it will go unpunished after attacking the greatest military power in the Middle East.

You can follow Lucas on X and Telegram.

April 6, 2024 Posted by | Ethnic Cleansing, Racism, Zionism, War Crimes | , , , , | 1 Comment

US using Nordic countries’ NATO membership to advance Arctic militarization

By Lucas Leiroz | April 6, 2024

The US plans to use the NATO access of Nordic countries to increase its military presence in the Arctic. In a recent statement, an American official announced Washington’s plan to build a large weapons warehouse in the region, with Finnish and Swedish support. The measure will significantly increase the militarization of the Arctic and aims to help the US overcome Russian military superiority in the region.

The plan was announced by US Materiel Commander Christopher Mohan during an interview with the newspaper Breaking Defense. According to him, Finland and Sweden could help the US with the project, considering their strategic geography. He did not give any details about the possible location of the depot, but stated that NATO is jointly analyzing all possibilities. He also stated that the US and allies are discussing what would be the most appropriate equipment to deploy in the region.

“The addition of the NATO partners changes the security landscape and our responsibilities as part of NATO (…) [This project will] embrace and integrate Finland and Sweden into the NATO enterprise, and that’s going to drive some changes on the ground,” he said.

The measure is just one of several policies adopted by Washington and its allies in recent years to try to reverse Russian military superiority in the Arctic. For decades, the US has not had any special focus on the Arctic in its defense strategies. The main objective of American strategic plans has always been to “encircle” and “isolate” Russia. The US has focused for many years on achieving this goal through the militarization of Europe and the destabilization of Central Asia and the Middle East, but Americans have paid little attention to the Arctic – a region where the Russians have become very strong over the decades.

Now, however, the US is concerned about this weakness in the region. With the escalation of tensions with Russia, Washington is trying to improve its positions in the Arctic in order to reverse the current scenario of Russian advantage. In recent years, several escalatory policies have been promoted by the US – some of them even openly provocative and targeted at Russia.

For example, in 2022, Lawrence Melnicoff, commander of the European Special Operations Command, stated that the US should actually “provoke” Russia in the Arctic. According to him, Washington should seek joint strategies with Norway to increase its presence in the Arctic Circle and thus deter Russia in the region. He states that Russia has expansionist plans that will be prevented only through direct deterrence, which is why NATO should maintain strategic positions that allow it to neutralize Russian forces in the Arctic in a possible conflict scenario.

“We are intentionally trying to be provocative without being escalatory (…) We’re trying to deter Russian aggression, expansionist behavior, by showing enhanced capabilities of the allies (…) It complicates Russian decision-making because we know that they’re targeting very, very large specific aggregations of allied power, [such as] Ramstein Air Base, RAF Lakenheath, things like that (…) If worse comes to worst and somebody takes out these power hubs, we can forward-project precision artillery fire across the alliance with our partners”, he said at the time.

Obviously, this is a fallacious US narrative. The Arctic is a region traditionally occupied by the countries that have access to it. Russia has the Arctic as a vital point in its strategic environment and naturally seeks to maintain a strong military presence in the region to guarantee its national security. The US and NATO countries, however, do not use access to the Arctic to develop a defensive strategy. On the contrary, they are looking for the Arctic as a possible point of attack against Russia. The Western objective in the Arctic is simply to harm Russia, not to protect itself. If the West adopted a policy of diplomacy and peaceful dialogue with Moscow, there would be no military race in the Arctic, but clearly NATO’s intention is to hurt Russia as much as possible.

To achieve these provocative objectives, the US will use the strategic location of NATO’s new members as a tool of war. The Nordic countries will be induced to actively participate in the Arctic militarization process, co-leading with Washington an escalation of tensions with Russia. And this will be extremely harmful for them, because, if the crisis escalates into an open conflict in the future, these countries will be priority targets and will be in a much greater risk zone for Russian attacks than the US.

Once again, access to NATO appears to be a trap for Finland and Sweden, which are being used as mere war tools by the US.

Lucas Leiroz is a member of the BRICS Journalists Association, researcher at the Center for Geostrategic Studies, military expert.

You can follow Lucas on X (former Twitter) and Telegram.

April 6, 2024 Posted by | Militarism | , , , , | Leave a comment