The Real Anthony Fauci: Bill Gates, Big Pharma, and the Global War on Democracy and Public Health

by Robert F. Kennedy Jr.

Despite its disappointing performance, Dr. Fauci worked hand-in-hand with Gilead’s remdesivir team to guide the trial to a satisfactory outcome.

Altering protocols in the middle of an ongoing study is an interference commonly known as “scientific fraud” or “falsification.” UCLA Epidemiology Professor Sander Greenland explains, “You’re not supposed to change your endpoint mid-course. That’s frowned upon.” Vera Sharav agrees: “Changing primary outcomes after a study has commenced is considered dubious and suspicious.”39

From that lofty platform, Dr. Fauci, with great fanfare, declared victory. The data from NIAID’s clinical trial for remdesivir shows “quite good news,” he said, glossing over the drug’s failure to demonstrate any mortality advantage.51 He boasted that the median time for hospitalization was eleven days for patients taking remdesivir, compared to fifteen days in the placebo group. He told the credulous press: “The data shows that remdesivir has a clear-cut, significant, positive effect in diminishing the time to recovery.” He claimed that his study had therefore proven remdesivir so remarkably beneficial to COVID patients that he had decided that it would be unethical to deny Americans benefits of this wonder drug. He was, he declared, unblinding and ending the study and giving remdesivir to the placebo group. Remdesivir would be America’s new “standard of care”52 for COVID. It was, of course, all a lie.

“Every independent randomized controlled trial of remdesivir has shown either a lack of benefit or a clear trend to harm,” says Dr. Pierre Kory. “It’s only those two Pharma studies (with Dr. Fauci) that show any benefits and even then, the benefits are minor.”

For several months, we were the only country treating people with a drug proven to be lethal. That year, 2020, we had almost double the number of deaths per month compared to most other countries. Brazil, one of the first nations to widely use remdesivir, had the second highest death toll.80,81

Dr. McCullough gives us a stark and clear summary: “Remdesivir has two problems. First, it doesn’t work. Second, it is toxic and it kills people.”

The first obstacle was the coronavirus’s tendency to rapidly mutate, producing vaccine-resistant variants. Vaccine developers like Hotez and Offit doubted that, after decades of futile efforts, researchers could suddenly develop a COVID vaccine that would provide “sterilizing immunity,” meaning that it would completely obliterate viral colonies in vaccinated individuals and prevent transmission and mutation.

Even worse, vaccinated individuals, he warned, would become asymptomatic carriers and “mutant factories” blasting out vaccine-resistant versions of the disease that were likely to lengthen and intensify rather than abbreviate the pandemic.

Vaccines are one of the rare commercial products that multiply profits by failing.

The even more daunting obstacle to coronavirus vaccines was their tendency to induce “pathogenic priming”—also known as “antibody-dependent enhancement” (ADE)—an overstimulation of immune system response that can cause severe injuries and death when vaccinated individuals subsequently encounter the wild viruses.

Dr. Hotez confessed to the committee that his colleagues had killed a number of children from pathogenic priming during experiments with the respiratory syncytial virus (RSV) vaccines in 1966, and recounted that during his own earlier work on coronavirus vaccines, he saw the same effect on ferrets:

We started developing coronavirus vaccines and our colleagues—we noticed in laboratory animals that they started to show some of the same immune pathology. So we said, “Oh my God, this is going to be problematic.”

Dr. Fauci’s first approach was to abort the three-year clinical trials at six months and then vaccinate the controls—a preemption that would prevent detection of long-term injuries, including pathogenic priming.

Second, as COVID czar, Dr. Fauci stubbornly refused to fix HHS’s designed-to-fail vaccine injury surveillance system (VAERS), which systematically suppresses reporting of most vaccine injuries.

Third, Dr. Fauci’s trump card was his capacity to enlist mainstream and social media companies to make reporting of injuries and deaths disappear from the airwaves, newspapers, and the Internet, and therefore from the public consciousness.

The Bill Gates-funded fact-checking organization, Politifact,18 worked with Pharma-funded fact-checkers like FactCheck, which receives, funding from the Robert Wood Johnson Foundation, and whose current CEO is Richard Besser, former acting head of the CDC,

which owns $1.8 billion in Johnson & Johnson stock19,20 to “debunk” stories and studies of vaccine injuries.

Dr. Robert Malone, the inventor of the...

“The real problem here is the damn press and the internet giants. The press and these tech players act to manufacture and reinforce ‘consensus’ around selected and approved narratives. And then this is being weaponized to attack dissenters, including highly qualified physicians.”21

Fourth, Dr. Fauci allowed CDC to discourage autopsies in deaths following vaccination.

Instead of exposing this sort of rank deception by government authorities, media and social media enablers emboldened HHS to new nadirs in regulatory malpractice. In January of 2021, baseball superstar Hank Aaron, whom I knew, died seventeen days after receiving the COVID jab at a CDC-sponsored press conference in Atlanta. I observed, in a Defender article,22 that Aaron’s death was one of a wave of deaths among the elderly following COVID jabs. This was true, but the New York Times nevertheless vilified me for spreading “misinformation” and claimed that the Fulton County Coroner had determined that Aaron’s death was “unrelated to vaccines.” USA Today, Newsweek, TIME, Daily Beast, ABC, CNN, and CBS reported the Times claim.23 But when I called to verify their claim, the Fulton County Coroner told me that the office has never seen Aaron’s body and that no autopsy was ever performed. Aaron’s family had buried the home-run hero without a postmortem. The Times’ fabrication was part of the systematic campaign of deception, propaganda, and censorship by HHS regulators in partnership with mainstream media—almost unprecedented in the American experience—that helped conceal the tsunami of vaccine injuries and fatalities.

Fifth, Dr. Fauci populated the key FDA and CDC committees with NIAID, NIH, and Gates Foundation grantees and loyalists to insure rubber-stamp approvals for his mRNA vaccines, without any long-term injury studies.

Sixth, by vaccinating the entire population, Dr. Fauci seems to be striving to eliminate the control group, to hide vaccine injuries.

Whether intentional or not, the effect of this escalation was, increasingly, to eliminate the control group—which, coincidentally, would permanently hide the evidence of vaccine injuries.

At this book’s November 2021 publication date, only Pfizer’s COVID vaccine, known as Comirnaty, had won FDA approval. Although Comirnaty is not yet given in the United States, its counterpart—the Pfizer-BioNTech, the same vaccine under a different name—is, so I will focus on the Pfizer-BioNTech vaccine.

The fact that FDA nevertheless granted Pfizer full approval, and that the medical community embraced and prescribed this intervention for their patients, is eloquent testimony to the resilience of even the most deadly and inefficacious products, and the breathtaking power of the pharmaceutical industry and its government allies to control the narrative through captive regulators, compliant physicians, and media manipulation, and to overwhelm the fundamental common sense of much of humanity.

The table shows that during the six-month trial, two people in the placebo group numbering approximately 22,000 and only one in the similarly sized vaccine group died from COVID. Believe it or not, this data point is the source of Pfizer’s claim that the vaccine is 100 percent efficacious against death.

“All-cause mortality” should be the key metric in weighing the value of any medical intervention. That measure alone tells us whether vaccinated individuals enjoy better outcomes and longer lives than the unvaccinated.

That means there were 42.8 percent more deaths in the vaccine than in the placebo groups.

This six-month safety report was so damning that it should have closed the case against this vaccine, but captured FDA officials nevertheless gave Pfizer their approval; the broken VAERS system and the mainstream and social media all conspired to conceal the evidence of the crime when vaccinated Americans began dying in droves, and CDC implemented its own retinue of enshrouding machinations to cloak the real-life carnage.

Critics suggest that the shocking and predictable rise in COVID death following vaccination is evidence of long-feared pathogenic priming.

The Johns Hopkins data, nevertheless, clearly demonstrate that COVID deaths typically spike sharply in many country after country immediately after mass vaccination.

In 1976, US regulators pulled the swine flu vaccine after it was linked to 25 deaths.

A recent peer-reviewed study in the high-gravitas Elsevier journal Toxicology Reports found that COVID-19 vaccines kill more people in each age group than they save. According to that study the “best-case scenario” is five times the number of deaths attributable to each vaccination vs. those attributable to COVID-19 in the most vulnerable 65+ demographic.

One of CDC’s bold deceptions is to hide vaccine mortalities in US data by counting all people as “unvaccinated” unless their deaths occur more than two weeks AFTER the second vaccine.

Walensky sheepishly admitted that CDC included hospitalization and mortality data from January through June 2021 in its calculation.76 The vast majority of the US population were, of course, unvaccinated during that time frame, so it makes sense that almost all hospitalizations would therefore be only among the unvaccinated.

Despite the obstacles to reporting, VAERS recorded nearly 800,000 injuries by the 9½ months between December 14, 2020 and October 2021, with 112,000 classified as “serious.” Pfizer either did not report several severe injuries—short of death—or deceptively deemphasized their severity, during clinical trials, including neurological harm, thrombocytopenia, blood clots, strokes, embolisms, aneurysms, myocarditis, Bell’s palsy, Guillain-Barré syndrome, multi-organ failure, amputation, blindness, paralysis, tinnitus, and menstrual harms. More than 30,000 women in the UK80 and 6,000 in the US have complained of the latter.

Pfizer’s clinical data predicted potentially fatal myocarditis in one in every 318 teens.

A recent study suggests that myocarditis is associated with a 50 percent mortality within five years.

In October 2021, Sweden, Denmark, and Finland announced that they will pause the use of Moderna’s COVID vaccine for children under 18 years of age, after increased reports of inflammatory diseases like myocarditis and pericarditis.

We have determined that an analysis of spontaneous postmarketing adverse events [VAERS reports] reported under section 505(k)(1) of the FDCA [Federal Food, Drug and Cosmetic Act] will not be sufficient to assess known serious risks of myocarditis and pericarditis and identify an unexpected serious risk of subclinical myocarditis. Furthermore, the pharmacovigilance system that FDA is required to maintain under section 505(k)(3) of the FDCA is not sufficient to assess these serious risks.

An October 3, 2021 study in the peer-reviewed journal BioRxiv by Stanford and Emory University scientists suggests that antibody levels generated by the Pfizer-BioNTech vaccine can suffer a ten-fold decrease seven months after the second vaccination.93 The scientists warn that the precipitous drop in antibody levels will compromise the body’s ability to defend itself against COVID-19 if the individual is exposed to COVID.

COVID-19 vaccines have caused cardiac arrest, blindness, and paralysis in American children.

Since the vaccine almost certainly causes more teen deaths and injuries than COVID-19, vaccinating this age group102 is highly unethical, and any physician who inoculates a healthy child is committing serious medical malpractice.

Illustratively, on September 10, 2021, an ABC affiliate in Detroit solicited stories on its Facebook page about unvaccinated people who had died from COVID. Instead, the network got something they did not want: more than 230,000 messages containing heartbreaking stories of injuries and deaths from vaccines. None of these communications were reporting deaths among the unvaccinated. Readers shared the post over two hundred thousand times in ten days.103

Under his watch, drug companies engineered the opioid crisis and made American citizens the globe’s most over-medicated population.

Dr. Fauci’s drug development enterprise is rife with other corrupting conflicts. Most Americans would be surprised to learn, for example, that pharmaceutical companies routinely pay extravagant royalties to Dr. Fauci and his employees and to NIAID itself.

In this document, the authors reported that the NIH has received, “up to $2 billion in royalty revenue for NIH since 1991, when FDA approved the first of these drugs. Three licenses generated more than $100 million each for the agency.”18

Dr. Fauci assigned most of these patents to universities, thereby making the ultimate commercial beneficiaries entirely opaque while binding the invaluable loyalty of American medical schools and the nation’s most influential physicians to Dr. Fauci and his policies.

Following drug approval, Dr. Fauci continues to collaborate with his pharmaceutical partners on promoting and pricing and profiting from their new product. Over the decades since Dr. Fauci took over NIAID, the agency has formalized an elaborate process of negotiating against US taxpayers to allow Pharma to extract maximum profits back from NIAID’s germinated drugs. With NIAID’s help, the lucky pharmaceutical company walks the new drug through accelerated FDA approval. The CDC then sets obscene retail prices for these collaborative products in secretive negotiations. Such sweetheart deals—at taxpayer and consumer expense—and accelerated approvals can yield direct financial benefits to NIAID, to Dr. Fauci’s favored employees, and even to Dr. Fauci himself.