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Brownstone Institute

The Great Game of Let’s Pretend

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11 minute read

From the Brownstone Institute

BY Jeffrey A. TuckerJEFFREY A. TUCKER  

Two nights ago was supposed to be a night of reckoning and truth. The intrepid and independent journalist Tucker Carlson was to grill Donald Trump, who skipped the GOP debates because he is already the hands-down frontrunner and doesn’t want anything to do with conventional politics.

Tucker had spent the last three years on Fox correctly denouncing lockdowns, censorship, vaccine mandates, and medical segregation, plus the attacks on American liberty. He certainly knows what’s what. One might have supposed that the issues that tanked the Trump presidency and nearly the whole of American society and liberty would be front and center. Now was the time!

Oddly, none of it came up in his interview with Trump. The interview answered none of our questions about why Trump did what he did, which not only wrecked the American economy but arguably lost him the election. Even if you think the election was stolen, it was only through the mail-in ballots that the Covid controls unleashed. Tucker drilled down into none of this. It was as if 2020 did not happen at all.

The simultaneous GOP debate was even worse. Ron DeSantis started with a bang and spoke about lockdowns but the topic fizzled quickly. Following a flurry of pharma ads – indeed the entire event was funded by FDA-approved drug sales – the moderators briefly asked former vice president Mike Pence if he thought his administration bore any responsibility for learning loss because the Trump administration urged school closures.

Pence – who spent 2020 running cover for Anthony Fauci and Deborah Birx – wholly ignored the question and said something else. The topic was never revisited again.

There was not one word said about tech censorship, the millions displaced and harmed by vaccine mandates, the dictatorial reach of the administrative state, the vast flurry of litigation against everything and everybody, the mass loss of trust in government and media, the foundational attack on the Bill of Rights, or the very real threat that it could happen again.

On the same day as the debate, we already saw mask mandates being reimposed. But no one spoke about it.

You surely see what’s going on here. The biggest issues in American life, which everyone experienced with vast tragedy and death all around, and about which everyone knows, are suddenly too sensitive to bring up. It’s something of which multitudes are aware but because all official institutions were involved, all official institutions are quiet about it. As a result, the great reckoning we need for renewal is farther off than ever.

Meanwhile, we’ve got Robert F. Kennedy, Jr., out there on countless public interviews, as a presidential candidate, saying remarkable things like 1) the CIA in 1963 killed his uncle who was president, 2) the intelligence community works with Big Pharma on gain-of-function research to create and cure new killer viruses, 3) they germ-gamed the lockdowns since 2001, 4) the lockdowns of March 2020 was a coup d’etat against representative democracy, 5) right now we have industry-captured Deep-State agencies that are ruling America who have no regard whatsoever for the US Constitution or the idea of freedom.

He says all of this without any shyness and with a great deal with knowledge and detail. He provides the receipts. Indeed, he has written several books on these themes. People listen and think “Oh that’s very interesting” and go hear him speak, without any presumption that he stands any chance to be President despite his wild popularity because, essentially, the fix is in.

Biden has already been selected to get the nomination, which rather demonstrates RFK’s point. Meanwhile, I’ve never once heard any reporter or read any article that challenges him on any of the facts. It’s as if everyone knows that what he is saying is true but we cannot do anything about it anyway. So he is tolerated as a wayward eccentric from a noble lineage but best ignored if we know what’s good for us.

It’s a very strange time in American political history, no doubt. We have one line of thinking sweeping through the population – which is based on mass incredulity and fury – and then another which is a veneer of normalcy that is slathered on top of our anger by all official institutions, which work hard to keep all these topics out of respectable conversations. Meanwhile, the whole of academic, mainstream social media, major mainstream media, and all of government seems to agree that all these obvious topics are too incendiary to be raised in polite company.

So everyone in the top layer of this manufactured consent is glad to play along with this great game of pretend. Meanwhile, people are fully aware now that the intelligence community is deeply involved in areas of life we previously thought were independent. And we suspect this is true even of organizations and publications we once thought were more-or-less trustworthy. How else to explain their silence and/or lies on all the crucial issues of our time?

As regards all the institutions that locked down the population just a few years ago, nothing has changed. Sure, there are a few court decisions extant that said they went too far but those are all being challenged and await appeals to the Supreme Court. But while these grueling processes play themselves out, Google, YouTube, Facebook, LinkedIn, and all the rest of our formerly free social-media platforms are more brutally censorial than ever. YouTube even announced that it will tolerate no content that contradicts the World Health Organization, which only three years ago recommended to the entire world the lockdowns pioneered by the CCP in Wuhan.

In the last few days, my own phone has blown up with people terrified of a new lockdown. They worry about leaving the country for fear of new travel restrictions. They worry about new vaccine mandates for their kids in school. They are thinking of moving to Florida and away from the big cities on the coasts where crime worsens by the day and skyscrapers are still mostly empty because workers won’t come back. And the #1 song in the world wails about the cruelty of this new world and how it is sending people to an early death.

Who would have imagined that a collapse on this level would happen in plain sight and everyone would see it and yet the entirety of the culture planners would in effect impose a fatwa on anyone who speaks about it?

Certainly I never imagined this scenario. Our whole lives we’ve sung about the “land of the free and the home of the brave” but here we are unfree and not brave. Because of facial-recognition technology, we cannot even hit the streets anymore. That was the real point of the post-January 6 crackdown: to serve as a lesson that if we resist in person, we will be recognized and dealt with severely.

The silence about the truth is utterly deafening. It’s not just that we aren’t getting answers to our questions; we aren’t even getting questions outside a handful of venues including this one.

Meanwhile, the highest hopes for saving the country from ruin are being placed in the hands of the very chief executive under whom all this began. And why? Because people believe that he was tricked and betrayed into greenlighting this wreckage even though he has never actually said anything like this. It’s the only hope people have. It’s a thin hope indeed.

When I first read Orwell’s 1984, it seemed like a dark and implausible fantasy and warning. I never imagined that it was really a reductio ad absurdum of a reality that he saw unfolding before him in the rising totalitarianism of his time. It turns out that he was a prophet of just how corrupt a highly politicized society with overweening bureaucracy can be in practice when careerism trumps courage and the cash nexus spreads the coercive mindset throughout all the commanding heights of the social order.

We are finding out now. The soundtrack of the end times is not Mahler or Wagner. It is gaming music with dance numbers on TikTok, with darkly distant echoes of a simple country singer in Virginia decrying the rich men north of Richmond.

Author

  • Jeffrey A. Tucker

    Jeffrey A. Tucker is Founder and President of the Brownstone Institute. He is also Senior Economics Columnist for Epoch Times, author of 10 books, including Liberty or Lockdown, and thousands of articles in the scholarly and popular press. He speaks widely on topics of economics, technology, social philosophy, and culture.

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Brownstone Institute

FDA Exposed: Hundreds of Drugs Approved without Proof They Work

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From the Brownstone Institute

By Maryanne Demasi

The US Food and Drug Administration (FDA) has approved hundreds of drugs without proof that they work—and in some cases, despite evidence that they cause harm.

That’s the finding of a blistering two-year investigation by medical journalists Jeanne Lenzer and Shannon Brownleepublished by The Lever.

Reviewing more than 400 drug approvals between 2013 and 2022, the authors found the agency repeatedly ignored its own scientific standards.

One expert put it bluntly—the FDA’s threshold for evidence “can’t go any lower because it’s already in the dirt.”

A System Built on Weak Evidence

The findings were damning—73% of drugs approved by the FDA during the study period failed to meet all four basic criteria for demonstrating “substantial evidence” of effectiveness.

Those four criteria—presence of a control group, replication in two well-conducted trials, blinding of participants and investigators, and the use of clinical endpoints like symptom relief or extended survival—are supposed to be the bedrock of drug evaluation.

Yet only 28% of drugs met all four criteria—40 drugs met none.

These aren’t obscure technicalities—they are the most basic safeguards to protect patients from ineffective or dangerous treatments.

But under political and industry pressure, the FDA has increasingly abandoned them in favour of speed and so-called “regulatory flexibility.”

Since the early 1990s, the agency has relied heavily on expedited pathways that fast-track drugs to market.

In theory, this balances urgency with scientific rigour. In practice, it has flipped the process. Companies can now get drugs approved before proving that they work, with the promise of follow-up trials later.

But, as Lenzer and Brownlee revealed, “Nearly half of the required follow-up studies are never completed—and those that are often fail to show the drugs work, even while they remain on the market.”

“This represents a seismic shift in FDA regulation that has been quietly accomplished with virtually no awareness by doctors or the public,” they added.

More than half the approvals examined relied on preliminary data—not solid evidence that patients lived longer, felt better, or functioned more effectively.

And even when follow-up studies are conducted, many rely on the same flawed surrogate measures rather than hard clinical outcomes.

The result: a regulatory system where the FDA no longer acts as a gatekeeper—but as a passive observer.

Cancer Drugs: High Stakes, Low Standards

Nowhere is this failure more visible than in oncology.

Only 3 out of 123 cancer drugs approved between 2013 and 2022 met all four of the FDA’s basic scientific standards.

Most—81%—were approved based on surrogate endpoints like tumour shrinkage, without any evidence that they improved survival or quality of life.

Take Copiktra, for example—a drug approved in 2018 for blood cancers. The FDA gave it the green light based on improved “progression-free survival,” a measure of how long a tumour stays stable.

But a review of post-marketing data showed that patients taking Copiktra died 11 months earlier than those on a comparator drug.

It took six years after those studies showed the drug reduced patients’ survival for the FDA to warn the public that Copiktra should not be used as a first- or second-line treatment for certain types of leukaemia and lymphoma, citing “an increased risk of treatment-related mortality.”

Elmiron: Ineffective, Dangerous—And Still on the Market

Another striking case is Elmiron, approved in 1996 for interstitial cystitis—a painful bladder condition.

The FDA authorized it based on “close to zero data,” on the condition that the company conduct a follow-up study to determine whether it actually worked.

That study wasn’t completed for 18 years—and when it was, it showed Elmiron was no better than placebo.

In the meantime, hundreds of patients suffered vision loss or blindness. Others were hospitalized with colitis. Some died.

Yet Elmiron is still on the market today. Doctors continue to prescribe it.

“Hundreds of thousands of patients have been exposed to the drug, and the American Urological Association lists it as the only FDA-approved medication for interstitial cystitis,” Lenzer and Brownlee reported.

“Dangling Approvals” and Regulatory Paralysis

The FDA even has a term—”dangling approvals”—for drugs that remain on the market despite failed or missing follow-up trials.

One notorious case is Avastin, approved in 2008 for metastatic breast cancer.

It was fast-tracked, again, based on ‘progression-free survival.’ But after five clinical trials showed no improvement in overall survival—and raised serious safety concerns—the FDA moved to revoke its approval for metastatic breast cancer.

The backlash was intense.

Drug companies and patient advocacy groups launched a campaign to keep Avastin on the market. FDA staff received violent threats. Police were posted outside the agency’s building.

The fallout was so severe that for more than two decades afterwards, the FDA did not initiate another involuntary drug withdrawal in the face of industry opposition.

Billions Wasted, Thousands Harmed

Between 2018 and 2021, US taxpayers—through Medicare and Medicaid—paid $18 billion for drugs approved under the condition that follow-up studies would be conducted. Many never were.

The cost in lives is even higher.

A 2015 study found that 86% of cancer drugs approved between 2008 and 2012 based on surrogate outcomes showed no evidence that they helped patients live longer.

An estimated 128,000 Americans die each year from the effects of properly prescribed medications—excluding opioid overdoses. That’s more than all deaths from illegal drugs combined.

A 2024 analysis by Danish physician Peter Gøtzsche found that adverse effects from prescription medicines now rank among the top three causes of death globally.

Doctors Misled by the Drug Labels

Despite the scale of the problem, most patients—and most doctors—have no idea.

A 2016 survey published in JAMA asked practising physicians a simple question—what does FDA approval actually mean?

Only 6% got it right.

The rest assumed that it meant the drug had shown clear, clinically meaningful benefits—such as helping patients live longer or feel better—and that the data was statistically sound.

But the FDA requires none of that.

Drugs can be approved based on a single small study, a surrogate endpoint, or marginal statistical findings. Labels are often based on limited data, yet many doctors take them at face value.

Harvard researcher Aaron Kesselheim, who led the survey, said the results were “disappointing, but not entirely surprising,” noting that few doctors are taught about how the FDA’s regulatory process actually works.

Instead, physicians often rely on labels, marketing, or assumptions—believing that if the FDA has authorized a drug, it must be both safe and effective.

But as The Lever investigation shows, that is not a safe assumption.

And without that knowledge, even well-meaning physicians may prescribe drugs that do little good—and cause real harm.

Who Is the FDA Working for?

In interviews with more than 100 experts, patients, and former regulators, Lenzer and Brownlee found widespread concern that the FDA has lost its way.

Many pointed to the agency’s dependence on industry money. A BMJ investigation in 2022 found that user fees now fund two-thirds of the FDA’s drug review budget—raising serious questions about independence.

Yale physician and regulatory expert Reshma Ramachandran said the system is in urgent need of reform.

“We need an agency that’s independent from the industry it regulates and that uses high-quality science to assess the safety and efficacy of new drugs,” she told The Lever. “Without that, we might as well go back to the days of snake oil and patent medicines.”

For now, patients remain unwitting participants in a vast, unspoken experiment—taking drugs that may never have been properly tested, trusting a regulator that too often fails to protect them.

And as Lenzer and Brownlee conclude, that trust is increasingly misplaced.

Republished from the author’s Substack

 

Author

Maryanne Demasi, 2023 Brownstone Fellow, is an investigative medical reporter with a PhD in rheumatology, who writes for online media and top tiered medical journals. For over a decade, she produced TV documentaries for the Australian Broadcasting Corporation (ABC) and has worked as a speechwriter and political advisor for the South Australian Science Minister.

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Brownstone Institute

Anthony Fauci Gets Demolished by White House in New Covid Update

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From the Brownstone Institute

By  Ian Miller 

Anthony Fauci must be furious.

He spent years proudly being the public face of the country’s response to the Covid-19 pandemic. He did, however, flip-flop on almost every major issue, seamlessly managing to shift his guidance based on current political whims and an enormous desire to coerce behavior.

Nowhere was this more obvious than his dictates on masks. If you recall, in February 2020, Fauci infamously stated on 60 Minutes that masks didn’t work. That they didn’t provide the protection people thought they did, there were gaps in the fit, and wearing masks could actually make things worse by encouraging wearers to touch their face.

Just a few months later, he did a 180, then backtracked by making up a post-hoc justification for his initial remarks. Laughably, Fauci said that he recommended against masks to protect supply for healthcare workers, as if hospitals would ever buy cloth masks on Amazon like the general public.

Later in interviews, he guaranteed that cities or states that listened to his advice would fare better than those that didn’t. Masks would limit Covid transmission so effectively, he believed, that it would be immediately obvious which states had mandates and which didn’t. It was obvious, but not in the way he expected.

And now, finally, after years of being proven wrong, the White House has officially and thoroughly rebuked Fauci in every conceivable way.

White House Covid Page Points Out Fauci’s Duplicitous Guidance

A new White House official page points out, in detail, exactly where Fauci and the public health expert class went wrong on Covid.

It starts by laying out the case for the lab-leak origin of the coronavirus, with explanations of how Fauci and his partners misled the public by obscuring information and evidence. How they used the “FOIA lady” to hide emails, used private communications to avoid scrutiny, and downplayed the conduct of EcoHealth Alliance because they helped fund it.

They roast the World Health Organization for caving to China and attempting to broaden its powers in the aftermath of “abject failure.”

“The WHO’s response to the COVID-19 pandemic was an abject failure because it caved to pressure from the Chinese Communist Party and placed China’s political interests ahead of its international duties. Further, the WHO’s newest effort to solve the problems exacerbated by the COVID-19 pandemic — via a “Pandemic Treaty” — may harm the United States,” the site reads.

Social distancing is criticized, correctly pointing out that Fauci testified that there was no scientific data or evidence to support their specific recommendations.

“The ‘6 feet apart’ social distancing recommendation — which shut down schools and small business across the country — was arbitrary and not based on science. During closed door testimony, Dr. Fauci testified that the guidance ‘sort of just appeared.’”

There’s another section demolishing the extended lockdowns that came into effect in blue states like California, Illinois, and New York. Even the initial lockdown, the “15 Days to Slow the Spread,” was a poorly reasoned policy that had no chance of working; extended closures were immensely harmful with no demonstrable benefit.

“Prolonged lockdowns caused immeasurable harm to not only the American economy, but also to the mental and physical health of Americans, with a particularly negative effect on younger citizens. Rather than prioritizing the protection of the most vulnerable populations, federal and state government policies forced millions of Americans to forgo crucial elements of a healthy and financially sound life,” it says.

Then there’s the good stuff: mask mandates. While there’s plenty more detail that could be added, it’s immensely rewarding to see, finally, the truth on an official White House website. Masks don’t work. There’s no evidence supporting mandates, and public health, especially Fauci, flip-flopped without supporting data.

“There was no conclusive evidence that masks effectively protected Americans from COVID-19. Public health officials flipped-flopped on the efficacy of masks without providing Americans scientific data — causing a massive uptick in public distrust.”

This is inarguably true. There were no new studies or data justifying the flip-flop, just wishful thinking and guessing based on results in Asia. It was an inexcusable, world-changing policy that had no basis in evidence, but was treated as equivalent to gospel truth by a willing media and left-wing politicians.

Over time, the CDC and Fauci relied on ridiculous “studies” that were quickly debunked, anecdotes, and ever-shifting goal posts. Wear one cloth mask turned to wear a surgical mask. That turned into “wear two masks,” then wear an N95, then wear two N95s.

All the while ignoring that jurisdictions that tried “high-quality” mask mandates also failed in spectacular fashion.

And that the only high-quality evidence review on masking confirmed no masks worked, even N95s, to prevent Covid transmission, as well as hearing that the CDC knew masks didn’t work anyway.

The website ends with a complete and thorough rebuke of the public health establishment and the Biden administration’s disastrous efforts to censor those who disagreed.

“Public health officials often mislead the American people through conflicting messaging, knee-jerk reactions, and a lack of transparency. Most egregiously, the federal government demonized alternative treatments and disfavored narratives, such as the lab-leak theory, in a shameful effort to coerce and control the American people’s health decisions.

When those efforts failed, the Biden Administration resorted to ‘outright censorship—coercing and colluding with the world’s largest social media companies to censor all COVID-19-related dissent.’”

About time these truths are acknowledged in a public, authoritative manner. Masks don’t work. Lockdowns don’t work. Fauci lied and helped cover up damning evidence.

If only this website had been available years ago.

Though, of course, knowing the media’s political beliefs, they’d have ignored it then, too.

Republished from the author’s Substack

Author

Ian Miller is the author of “Unmasked: The Global Failure of COVID Mask Mandates.” His work has been featured on national television broadcasts, national and international news publications and referenced in multiple best selling books covering the pandemic. He writes a Substack newsletter, also titled “Unmasked.”

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