Brownstone Institute
Congressional Committee Condemns (Nearly) Every Feature of the Covid Response
From the Brownstone Institute
The conclusion of the report: nothing worked and everything tried resulted in more damage than the pandemic could ever have achieved on its own. In this sense, and given the low bar of expectations for all such political commissions, every champion of truth, honesty, and freedom should celebrate this report.
Are there words in the English language that fully describe what happened during the Covid years that are not already overused? Calamity comes to mind. Disaster. Cataclysm. Ruin, devastation, catastrophe, unprecedented debacle, fiasco, and utter wreckage – all fine words and phrases but nothing quite captures it.
Given that, there is probably no report on the thing that can properly characterize the whole of it. On the other hand, it’s worth trying.
Meanwhile, the results of Covid commissions of governments around the world have become unbearably predictable. So far they have mostly said their government failed because they didn’t act fast enough, did not enforce lockdowns hard enough, did not communicate and coordinate well enough, and so on.
Everyone in the corporate world knows that when a committee reduces all problems to “communication and coordination” you are being fed a load of bull.
So far, it’s been almost entirely bureaucratic blather, and that helps account for the global loss of confidence in political systems. They cannot even be honest about the most catastrophic policies in our lifetimes or several.
The amount of corruption, waste, and destruction from this period of our lives, lasting from 2020 until 2023 but with remnants of bad policies all around us, is so unspeakable that not one report has yet been fully honest about what happened, why it happened, who really won and lost, and what this period implies for how vast swaths of the public see the world.
Among other astonishing revelations to come from this period was a full presentation of just how many institutions have been corrupted. It was not just governments and certainly not just the elected leaders and career bureaucrats. The problems are very deep and reach more deeply to intelligence agencies, military-based bioweapons systems, and preparedness agencies that guard their activities under the cloak of what is called classified.
This is a major reason why so many questions are being left unasked and unanswered. Then we have the ancillary failures in a whole series of additional sectors. The media went along with the nonsense as if they are wholly owned and controlled by government and industry. Industry mostly went along too, at least the highest reaches of it, even as small business was crushed.
The tech companies cooperated in a massive censorship operation. The retail end of the pharmaceutical companies enforced the government’s edicts, denying people basic medicines, as did the whole of the medical systems, which heavily enforced mandates on an experimental and failed product mistakenly called a vaccine. Academics were largely silent and public intellectuals fell in line. Most mainline religions cooperated in locking worshippers out. Banks were in on it too. And advertisers.
In fact, it’s hard to think of any institution in society that leaves this period untarnished. It’s probably not possible for a government report on the subject to be fully honest. Maybe it is too soon, plus the hooks that created the whole problem are still embedded too deeply.
All that said, we’ve got a solid start with the highest-level government report produced to date: After Action Review of the Covid-19 Pandemic: The Lessons Learned and a Path Forward, by the Select Subcommittee on the Coronavirus Pandemic as assembled by the US House of Representatives. The report was written by the majority and it shows.
Coming in at 550 pages with 2,000-plus footnotes (we have made a physical version available here), the preparation involved hearing from hundreds of witnesses, reading thousands of documents, listening to thousands of reports and interviews, and working at a furious pace for two years. Based on the outline and breadcrumbs of the Norfolk Group, while adding in additional material based on critiques of media and economic policy, it is a comprehensive blast against the public-health features of the pandemic response.
The conclusion of the report: nothing worked and everything tried resulted in more damage than the pandemic could ever have achieved on its own. In this sense, and given the low bar of expectations for all such political commissions, every champion of truth, honesty, and freedom should celebrate this report. It is an excellent breaking of the ice around the topic. Note that this report has received very little press attention, which only further underscores the problem.
Coming in for heavy criticism: gain-of-function research, the deference to the WHO, the lab-leak coverup, the funding of pharma cutouts, business and school closures, mask mandates, the lack of serious attention to disease monitoring, vaccine mandates, the sloppy approval process, the vaccine injury system, the banning of off-the-shelf therapeutics, social distancing, the rampant fraud in business loans, the effects of monetary policy, and more.
The report contains nuggets that we cannot help but praise:
Ignored in the report: the rental moratorium, the frenzy of Plexiglas and air filtration, the push for sanitizing all things, the reopening racket designed to prolong lockdowns, domestic capacity restrictions, the division of the workforce between essential and nonessential, the role of CISA and the intelligence agencies, the CDC’s push for mail-in ballots that might have been decisive in the national election, and the astonishing gibberish over the infection fatality and case fatality rates.
There is so much more to chronicle and criticize that the report could have been 10 or 100 times as long.
To be sure, the report has plenty of problems aside from these exclusions. Operation Warp Speed comes in for praise for saving “millions” of lives but the citation is to a modeling exercise that assumes what it is trying to prove. Look at the footnote: It’s bad science.
The real trouble with this section is not even its incorrect claim that the vaccine saved lives. The core issue is that the whole point of the lockdowns and all that followed was to create conditions for the release of the countermeasure. The plan from the beginning was: lockdown until vaccination. Praising the goal while criticizing the ineffective means diverts the point.
This is precisely what was explained to me in the early days in a phone call from a member of George W. Bush’s biosecurity team, a man who now runs a vaccine company. He said we would stay locked down until the world’s population got a shot in the arm. This phone call happened in April 2020.
Quite simply, I thought he had lost his mind and hung up. I did not believe that 1) the plan was always to stay in lockdowns until vaccination, and that 2) anyone seriously believed that governments could vaccinate their way out of a wave of respiratory infections insofar as the pathogen had a zoonotic reservoir.
The very idea struck me as so preposterous that I was incredulous that an educated and responsible adult could ever advance it. And yet that was precisely the plan all along. Sometime in the last week of February 2020, a global cabal decided to pull the trigger on a worldwide campaign of shock and awe – tapping every asset in civil society for assistance – to bring about worldwide forced medicalization with a new technology.
This was never really a public health response. That was only the cover story. This was a coup against science and against democracy, for purposes of industrial and political reset, not just in one nation but all nations at once. I get it: that is an ominous statement and hard to wrap one’s brain around the whole of it. In completely ignoring this point, the Select Subcommittee has missed the forest for the trees.
Let’s attempt a different metaphor. Let’s say your car is hijacked in Manhattan and you are thrown in the backseat. The goal is to drive all the way to Los Angeles for a drug deal. You could object to the means and goal but instead you spend the entire trip complaining about potholes, reckless driving, warning of the need for an oil change, and complaining about the bad music playing on the car radio.
At the end of the trip, you put out a report to this effect. Do you think that would be strange, to wholly ignore the theft of your car and the destination and purpose of the hijacking and instead focus on all the ways in which the grand larceny could have been smoother and happier for everyone involved?
In that spirit, the Subcommittee’s separate recommendations list is weak, leaving governments wholly in charge of anything labeled a pandemic while only suggesting a more cautionary approach that takes into consideration all costs and benefits. For example, it says on travel restrictions: “It is far easier to undo the restrictions that may have been unneeded than it is to take a ‘wait and see’ approach once the unknown virus of concern has entered our borders and thoroughly spread.”
It seems like the core lesson – governments cannot be masters of the microbial kingdom and allowing them to pretend otherwise for purposes of an industrial and political reset cues up a moral hazard that is an ongoing threat to freedom and rights – is not yet learned, or even so much as admitted. We are still being invited to believe that the same people and institutions who created calamity last time should be trusted again next time.
And keep in mind: this is the best report yet issued!
My friends, we have a very long way to go to absorb the fullness of the reality of what was done to individuals, families, communities, societies, and the whole world. Nor is it truly possible to move on without a full accounting of this disaster. Has it begun? Yes, but there is a very long way to go.
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
The Quiet Invasion: How Transnational Crime and Chinese State Actors Infiltrated Vancouver and Eroded Canada’s Sovereignty
Boxing authority says allegedly male competitor should return Olympic medal won against women
Canada’s euthanasia regime is not health care, but a death machine for the unwanted
Alberta’s government is investing $5 million to help launch the world’s first direct air capture centre at Innisfail
-
Alberta8 hours agoAlberta Independence Seekers Take First Step: Citizen Initiative Application Approved, Notice of Initiative Petition Issued
-
Automotive1 day agoElectric vehicle sales are falling hard in BC, and it is time to recognize reality.
-
Automotive1 day agoPower Struggle: Electric vehicles and reality
-
Business10 hours agoCanada Caves: Carney ditches digital services tax after criticism from Trump
-
Crime10 hours agoSuspected ambush leaves two firefighters dead in Idaho
-
Business1 day agoTrump on Canada tariff deadline: ‘We can do whatever we want’
-
Alberta8 hours agoWhy the West’s separatists could be just as big a threat as Quebec’s
-
Brownstone Institute2 days ago
FDA Exposed: Hundreds of Drugs Approved without Proof They Work