Brownstone Institute
This Was Tucker Carlson’s “Greatest Public Mistake”
From the Brownstone Institute
A new biography of Tucker Carlson offers a very interesting look at the intellectual odyssey of the most popular commentator in the US if not the world. Particularly interesting is his turnabout on the pandemic response.
Today he is a mighty critic of lockdowns and forced vaccination. But it was not always so. His voice was massively influential both in inspiring the lockdowns and warming conservatives up to the idea of panic.
Most devastatingly, in the first week of March, one week before the lockdowns, Tucker flew to Mar-a-Lago – his first time there – to meet with Trump and tell him that he was completely wrong that this pandemic required no extraordinary response. Instead he needed to act now.
The book explains:
The strength of Tucker’s bond with Trump was apparent on March 7, 2020, when he went to Mar-a-Lago to press his rising concerns about Covid-19 to the president personally. At the time almost all other conservative commentators were downplaying the threat of the virus — and their liberal counterparts, in a frenzy over the first Trump impeachment, were likewise giving it short shrift — but Tucker’s sources were telling him that Beijing was lying, the devastation in China was massive, and what was coming here was going to be catastrophic.
“I told him,” Carlson acknowledges now of his meeting with the president, “he could easily lose the election over Covid.” A couple of days later, he was sounding the warning in equally blunt terms to his audience. “People you trust, people you probably voted for, have spent weeks minimizing what is clearly a very serious problem,” he said. “‘It’s just partisan politics,’ they say. ‘Calm down. In the end this was just like the flu and people die from that every year. Coronavirus will pass.”
Such people, he continued, were “wrong,” what was coming would be “major,” and “It’s definitely not just like the flu. . . . The Chinese coronavirus will get worse; its effects will be far more disruptive than they are right now. That is not a guess; it is inevitable no matter what they’re telling you. Let’s hope everyone stops lying about that, and soon.”
The timeline of events confirms Tucker’s influence on Trump but Trump surely had others leaning on him as well. Following the meeting, Trump was not fully persuaded and Tweeted out on March 9 that this would come and go like the flu.
The very next day, he had flipped in the other direction.
How much influence did Tucker have? Some and maybe much over Trump. Just as important was the way in which his show itself drove conservatives to the point of panic. Following lockdowns, and within weeks, he reversed himself.
A major part of the next two years of his show was dedicated to debunking all that he had contributed in February and half of March. The book reports that Tucker Carlson regards his panic over the virus as the “great public mistake he ever made.”
It’s not as if Tucker himself made up the idea that Covid was going to be Ebola but widespread. As this book reports, “Tucker’s sources were telling him” that this would be true.
Tucker himself elaborated on the events in an interview for Vanity Fair that appeared on March 17, 2020. He explains:
Well, in January is when we first started covering it on the show. And you know, there’ve been a number of epidemics to come out of China—the 1957 flu epidemic, which killed 100,000 people in this country. And so when these reports began to emerge, we covered it….
And then I happened to be speaking a couple of days later to someone who works in the U.S. government, a nonpolitical person with access to a lot of intelligence. He said the Chinese are lying about the extent of this. They won’t let international health inspectors in. They’re blocking WHO and this could infect millions of people, a high percentage of them. And this was a highly informed person, very informed, and again, a nonpolitical person with no reason to lie about it in either direction.
So that really got my attention.
It was at this point that he decided to tell Trump what he had heard.
I felt I had a moral obligation to be useful in whatever small way I could, and, you know, I don’t have any actual authority. I’m just a talk show host. But I felt—and my wife strongly felt—that I had a moral obligation to try and be helpful in whatever way possible. I’m not an adviser to the person or anyone else other than my children. And I mean that. And you can ask anybody in the White House or out how many times have I gone to the White House to give my opinion on things. Because I don’t do that. And in general I really disapprove of people straying too far outside their lanes and acting like just because they have solid ratings, they have a right to control public policy. I don’t believe that. I think it’s wrong.
I don’t want to be that guy, and I’m not that guy, but I felt under this circumstance that it was something small that I could do. And again, I felt a moral obligation to do it, and I kept it secret because I was embarrassed of it because I thought that it was on some level wrong.
And think about the timing of this fair and affectionate interview itself. It is from a very hostile venue but they let Tucker have his say, with no smears. That itself is suspicious. And this interview appeared the day following the lockdown edicts. It was obviously important to someone that Tucker Carlson, the hero of the right, bless this panic that led to the dismantling of the economic and social order.
At that point in the timeline, Tucker was still dedicated to his story. He even had Covid at the time. He would not go near his children. “Nope. I’m not gonna. I’m waving at them through glass right now.”
We should not underestimate Tucker’s influence on all of this. The lockdowns – the wrecking of American liberty – certainly needed bipartisan and broad ideological support. If this became a left-right issue, it simply could not work. Therefore someone or something believed it was extremely important that Tucker needed to be convinced. And it worked.
Tucker has never revealed his source. He has never said who this person is: “someone who works in the U.S. government, a nonpolitical person with access to a lot of intelligence.” It was clearly someone he trusted and perhaps someone everyone in his circles trusted. And why has Tucker not revealed the source? Most likely because it was someone with high-level security clearances who then swore him to eternal secrecy. As a man of principle, he has done that.
There is one major figure who fits this description, more than anyone else. It is Matthew Pottinger, a member of the National Security Council and a person with high-level security contacts. His role in the pandemic response is very well documented. Most famously, it was he who pulled Deborah Birx out of her work on AIDS to head Trump’s virus commission. Pottinger is a well-known figure in the DC cocktail circuit and widely trusted by the “China hawks” in Washington. His security clearances gave him access and credibility.
In September 2019, Pottinger was named Deputy National Security Advisor, second only to National Security Advisor Robert O’Brien. From late January and following, he worked to spread alarm about the virus. He says that he spoke to medical doctors in China who told him that this was nothing like SARS-1 and has more in common with 1918. He went on to argue for lockdowns, universal masking, and even promoted the use of Remdesivir though he had no background at all in medicine or pharmaceuticals.
The most comprehensive study in print on Matthew Pottinger’s role is at Brownstone and written by Michael Senger. He sums up:
Pottinger may have simply been overly-trusting of his sources, thinking they were the little people in China trying to help their American friends. But why did Pottinger push so hard for sweeping Chinese policies like mask mandates that were far outside his field of expertise? Why did he so often breach protocol? Why seek out and appoint Deborah Birx?
It’s all very interesting but we should not underestimate the importance of this turn of events and the likely role of Pottinger in convincing Tucker of the case for tremendous alarm and panic. Without that, Trump might not have caved and the base would have rallied around him.
Instead, we got a response that effectively deleted the Bill of Rights, ruined economic and civil liberty, wrecked the Trump presidency, and triggered a new era in American life in which intelligence agencies and the administrative state under Biden have completely swamped the Founders’ vision of a self-governing people.
To Tucker’s credit, he sees this as his great mistake. But there is still more to know on how precisely this happened and why.
Author
From the Brownstone Institute
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 Brownlee, published 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.
- Investigative report by Jeanne Lenzer and Shannon Brownlee at The Lever [link]
- Searchable public drug approval database [link]
- See my talk: Failure of Drug Regulation: Declining standards and institutional corruption
Republished from the author’s Substack
Author
From the Brownstone Institute
By 
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
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