White House Expands Vaccine Mandate To Cover 80 Million Workers
By Tyler Durden | Zero Hedge | November 4, 2021
The White House has just released new policies requiring all companies – big and small – to coerce their workers into accepting the vaccine, or face termination, as the Biden Administration continues to up the pressure on all working Americans to get vaccinated before Jan. 4.
According to Axios, President Biden is planning to announce Thursday that employers with more than 100 workers on their payroll must guarantee that their workers are fully vaccinated, or tested weekly, by Jan. 4, 2022. If not, they could face federal fines starting at tens of thousands of dollars per offense.
What’s more, health-care workers will face even tougher restrictions which will effectively require every health-care worker in the country to be vaccinated, or lose their job, despite the fact that millions of health-care workers have already been infected with the virus by natural means.
To be sure, managing weekly testing programs for a minority of corporate employees will be extremely costly, and the ramifications of this new policy will essentially force employees for the biggest companies in the US to accept the vaccine.
Per Axios, the new rules – formally known as the COVID-19 Vaccination and Testing Emergency Temporary Standard – will be enforced by OSHA. They will affect roughly two-thirds of America’s workforce, or roughly 80MM people. Many businesses and hospitals have already started to enforce vaccine mandates, and while Axios reports that they have seen “minimal” noncompliance, that doesn’t exactly square with the fact that less than 60% of the American population is fully vaccinated.
While corporations might be able to absorb some of these costs, small businesses will likely be left with some difficult decisions to make. However, there’s one important catch: OSHA will mostly rely on “complaints” to enforce the rule, meaning it will be up to American workers whether or not they want to hold their fellow workers accountable for defying the policy. This incentive to snitch out co-workers and neighbors has already elicited criticism from some, including Conservative Radio host Dan Bongino, who has pushed back against vaccine mandates in favor of bodily autonomy.
The strict mandate for health-care workers is already creating some problems because, while 40% of health-care businesses have purportedly already enforced the policy, the supposedly “minimal” level of noncompliance is reportedly exacerbating worker shortages at hospitals and other critical service providers.
In another indication of how companies are struggling with the mandate, some federal contractors had been expected to enforce the Biden Admin’s vaccine mandate by Dec. 8, but those expectations have now been pushed back to Jan. 4. When asked whether the pushback was due to worker shortages, or the timing of the holiday season, they refused to comment, saying only that the delay is meant to “align” with health-care facilities and US employers.
Perhaps President Biden (and VP/President-in-waiting Kamala Harris) have already forgotten the lessons of Tuesday’s “off-year” election?
Pfizer Is Calling The Shots To Jab Kids
Dr. Joseph Mercola | November 1, 2021
In late February 2021, The Bureau of Investigative Journalism reported1 that Pfizer was demanding countries put up sovereign assets as collateral for expected vaccine injury lawsuits resulting from its COVID-19 inoculation.
While at least two countries, Argentina and Brazil, initially rejected the demands, calling them abusive, many others accepted Pfizer’s terms from the start.
Public Citizen has now reviewed and published the secret contracts2,3 between Pfizer and Albania, Brazil, Colombia, Chile, Dominican Republic, the European Commission, Peru, the U.S. and the U.K. These contracts reveal nations have handed over unprecedented power to Pfizer. In virtually all scenarios, Pfizer’s interests come first.
Pfizer Is Calling The Shots
Public Citizen points out six ways in which nations are allowing Pfizer to call the shots. For example, Albania, Brazil and Colombia have handed over unilateral authority to the company for the delivery schedule and other key decisions. As reported by Public Citizen:4
“As a condition to entering into the agreement, the Colombian government is required to ‘demonstrate, in a manner satisfactory to Suppliers, that Suppliers and their affiliates will have adequate protection, as determined in Suppliers’ sole discretion’ … from liability claims.
Colombia is required to certify to Pfizer the value of the contingent obligations (i.e., potential future liability), and to start appropriating funds to cover the contingent obligations, according to a contribution program.”
Pfizer also maintains tight control over vaccine supplies, and dictates who can buy their vaccine, when, and who can give and receive vaccine donations. If there are shortages, Pfizer decides which countries get priority.
Bypassing Pfizer can be costly. For example, if Brazil were to accept vaccine donations from another country without Pfizer’s approval, the company can terminate the contract and force Brazil to pay the full prize for all remaining contracted doses. Meanwhile, Pfizer incurs no penalty if its delivery is late, even if it’s so late that the shots are no longer needed.
Some countries, including Brazil, Chile, Colombia, the Dominican Republic and Peru, also ended up agreeing to Pfizer’s demand to put up sovereign assets as collateral for vaccine injury lawsuits, including bank reserves, military bases and embassy buildings.
In short, theses governments are guaranteeing Pfizer will be compensated for any expenses resulting from injury lawsuits against it, so the company won’t lose a dime if its COVID shot injures people — even if those injuries are the result of negligent company practices, fraud or malice!
At the same time, government purchasers must acknowledge that the effectiveness and safety of the shots are completely unknown. This is the ultimate corporate maleficence, using their leverage to force the kill shot down these countries’ throats and avoiding any personal responsibility for damages.
Secret Arbitration
The contracts also dictate how contractual disputes will be settled. As reported by Public Citizen:5
“What happens if the United Kingdom cannot resolve a contractual dispute with Pfizer? A secret panel of three private arbitrators — not a U.K court — is empowered under the contract to make the final decision. The arbitration is conducted under the Rules of Arbitration of the International Chamber of Commerce (ICC). Both parties are required to keep everything secret:
‘The Parties agree to keep confidential the existence of the arbitration, the arbitral proceedings, the submissions made by the Parties and the decisions made by the arbitral tribunal, including its awards, except as required by Law and to the extent not already in the public domain.’
The Albania draft contract and Brazil, Chile, Colombia, Dominican Republic, and Peru agreements require the governments to go further, with contractual disputes subject to ICC arbitration applying New York law. While ICC arbitration involving states is not uncommon, disputes involving high-income countries and/or pharmaceuticals appear to be relatively rare
Private arbitration reflects an imbalance of power. It allows pharmaceutical corporations like Pfizer to bypass domestic legal processes. This consolidates corporate power and undermines the rule of law.”
Pfizer Secured Intellectual Property Rights
Amazingly, the contracts not only secure Pfizer’s intellectual property rights, but should Pfizer be found guilty of stealing the intellectual property rights of others, some of the contracts shift the responsibility away from Pfizer onto the government purchasers! What this means is that Pfizer can steal the intellectual property of others without consequence in at least four countries.
“For example, if another vaccine maker sued Pfizer for patent infringement in Colombia, the contract requires the Colombian government to foot the bill,” Public Citizen writes.6 “Pfizer also explicitly says that it does not guarantee that its product does not violate third-party IP, or that it needs additional licenses.
Pfizer takes no responsibility in these contracts for its potential infringement of intellectual property. In a sense, Pfizer has secured an IP waiver for itself. But internationally, Pfizer is fighting similar efforts to waive IP barriers for all manufacturers.”
Pfizer Given Right To Silence Governments
Perhaps most egregious of all, some of the contracts give Pfizer the right to muzzle government. In Brazil, government officials are prohibited from making “any public announcement concerning the existence, subject matter or terms of [the] Agreement” without the written consent of the company.
The gag order also includes commenting on the government’s relationship with Pfizer in general. Similar nondisclosure provisions are included in the contracts with the European Commission and the U.S. government. The only difference, Public Citizen notes, is that the nondisclosure rules apply to both parties.
Pfizer Can Prevent Use Of Other Remedies
Equally shocking, though, is that countries are forced to follow through on their vaccine orders even if other drugs or treatments emerge that can prevent, treat or cure COVID-19.7 Is it any wonder, then, that governments around the world have suppressed the use of drugs like hydroxychloroquine and ivermectin?
If these drugs were allowed to be used and could be proven to work, the COVID injections would be completely unnecessary, yet governments are on the hook for hundreds of millions of doses. While COVID-19 vaccines are “free” to receive in the U.S., they’re being paid for by taxpayer dollars at a rate of $19.50 per dose. In Albania, the cost of each dose is $12, and in the EU, $14.70.
In the case of the price disparity between the U.S. and the EU, Pfizer is said to have given a price break to the EU because it financially supported the development of their COVID-19 vaccine.
As noted Public Citizen, Pfizer is being allowed to profit from this self-inflicted global disaster in unprecedented ways. In many instances, a nation’s laws will not apply to Pfizer.
These secret contracts grant Pfizer total control over its product and ensures full payment, regardless of whether the shots are needed or usable, while simultaneously eliminating all liability. In short, Pfizer wins, no matter what the outcome of the vaccination campaign might be.
At the same time, Pfizer is also controlling media through its advertising dollars. As you’ve probably realized by now, media companies in most instances will not report on anything that might jeopardize the profits of its advertisers.
As illustrated in the short video above, it couldn’t be more obvious that Pfizer is bankrolling the media, which in turn will refuse to bite the hand that feeds it. You can see the wide spectrum of media programming being sponsored by Pfizer, including “Nightline,” “Making a Difference,” “CNN Tonight,” “Early Start,” “Erin Burnett Out Front,” “This Week with George Stephanopoulos,” “CBS Sports,” “Meet the Press,” “CBS This Morning” and “60 Minutes.”
The terms of these contracts are all the more disturbing when you consider how dangerous the Pfizer shot is turning out to be. No wonder the company refused to accept any liability.
According to Pfizer’s own data, one COVID death per 20,000 fully vaccinated individuals is prevented. That means 10,000 lives are saved if 200 million are fully vaccinated.
But how many lives are lost from the shots? This is the other side of the equation that simply demands to be analyzed before any governmental authority can make a decision as to whether the mass vaccination campaign is of benefit or not.
Here, we find that Pfizer’s data10 show the shots are actually killing more than they save. To look at this information yourself, click on “Supplementary Material” on the right-hand side of the paper, then, beside Supplementary Appendix, click on supplements/261159 and scroll down to page 12, Table S4.
In the vaccine group, 15 died; in the placebo group 14 died. Two people died from COVID-19 in the placebo group, while only one died from COVID pneumonia in the vaccine group. That’s how you get a net false positive impact — one life is spared from COVID. However, the all-cause mortality was actually higher in the vaccine group (15, compared to 14).
So, while the shots saved one person from dying from COVID, they also killed one extra person. So, the net effect is nil. There’s no mortality benefit at all. Other investigations using different data strongly suggest the net effect is profoundly negative, and the shots are doing FAR more harm than good.
We Face Looming Vaccine-Induced Public Health Catastrophe
For this, Kirsch cites a paper11 by Dr. Bart Classen, published in the August 2021 issue of the journal Trends in Internal Medicine. Classen points out that Pfizer, Moderna and Janssen are all using a “dangerously misleading” clinical trial design. The problem is that they’re all using a surrogate endpoint for health, namely “severe infections with COVID-19.”
Disease specific primary endpoints are no longer used in many fields of medicine, for the fact that it can hide problems. If a person dies from the treatment or is severely injured by it, even if the treatment helped block the progression of the disease they’re being treated for, the end result is still a negative one.
For this reason, the appropriate endpoint that should be used is all-cause mortality and morbidity. When Classen reexamined the clinical trial data from all three manufacturers using all-cause severe morbidity as the endpoint, a disturbing picture emerged.
As explained by Classen in his paper, “US COVID-19 Vaccines Proven to Cause More Harm than Good Based on Pivotal Clinical Trial Data Analyzed Using the Proper Scientific Endpoint, ‘All Cause Severe Morbidity’”:12
“‘All-cause severe morbidity’ in the treatment group and control group was calculated by adding all severe events reported in the clinical trials. Severe events included both severe infections with COVID-19 and all other severe adverse events in the treatment arm and control arm respectively.
This analysis gives reduction in severe COVID-19 infections the same weight as adverse events of equivalent severity. Results prove that none of the vaccines provide a health benefit and all pivotal trials show a statistically significant increase in ‘all-cause severe morbidity’ in the vaccinated group compared to the placebo group.
The Moderna immunized group suffered 3,042 more severe events than the control group. The Pfizer data was grossly incomplete but data provided showed the vaccination group suffered 90 more severe events than the control group, when only including ‘unsolicited’ adverse events.
The Janssen immunized group suffered 264 more severe events than the control group. These findings contrast the manufacturers’ inappropriate surrogate endpoints:
Janssen claims that their vaccine prevents 6 cases of severe COVID-19 requiring medical attention out of 19,630 immunized; Pfizer claims their vaccine prevents 8 cases of severe COVID-19 out of 21,720 immunized; Moderna claims its vaccine prevents 30 cases of severe COVID-19 out of 15,210 immunized.
Based on this data it is all but a certainty that mass COVID-19 immunization is hurting the health of the population in general. Scientific principles dictate that the mass immunization with COVID-19 vaccines must be halted immediately because we face a looming vaccine induced public health catastrophe.”
To make the above numbers more clear and obvious, here are the prevention stats in percentages:
- Pfizer 0.00036 percent
- Moderna 0.00125 percent
- Janssen 0.00030 percent
CDC Claims COVID Shots Lower All-Cause Mortality
Despite all of that, the U.S. Centers for Disease Control and Prevention now claims Americans “vaccinated” against COVID-19 have lower all-cause mortality rates.13 As reported by Forbes:14
“Partially and fully vaccinated people died from non-coronavirus causes at a lower rate than their unvaccinated peers, according to the study,15 which looked at millions of patients at seven U.S. health organizations from December to July.
All three vaccines approved by U.S. regulators were tied to lower non-COVID death rates, though the difference in mortality among people who took Johnson & Johnson’s vaccine was slightly smaller than for recipients of Pfizer or Moderna’s vaccines …
This result suggests the vaccines don’t increase a patient’s risk of death, which ‘reinforces the safety profile of currently approved COVID-19 vaccines,’ the study said.”
October 26, 2021, the FDA unanimously voted to grant emergency use approval of the COVID shots for children between the ages of 5 and 11.16 This despite acknowledging they have no idea what the long-term risk to children might be. As noted by one voting member, “We’re never going to learn about how safe the vaccine is until we start giving it.”17
All we have at present is two Pfizer trials, one in which 5- to 11-year-olds were followed for two months and another with just six weeks of follow-up. Both were too small to detect potential risks such as myocarditis. That won’t be studied until AFTER the shot is authorized for children. As reported by The Defender :18
“Experts raised concerns over the lack of safety and efficacy data presented by Pfizer for use of its COVID vaccine in younger children, and they pointed to increasing safety signals based on reports to the Vaccine Adverse Event Reporting System (VAERS). They also questioned the need to vaccinate children — whose risk of dying from COVID is “almost nil” — at all.
According to Dr. Meryl Nass, member of the Children’s Health Defense Scientific Advisory Panel, Pfizer once again did not use all of the children who participated in the trial in their safety study.
‘Three thousand children received Pfizer’s COVID vaccine, but only 750 children were selectively included in the company’s safety analysis,’ Nass said.
‘Studies in the 5-11 age group are essentially the same as the 12-15 group — in other words, equally brief and unsatisfying, with inadequate safety data and efficacy data, with no strong support for why this type of immuno-bridging analysis is sufficient … All serious adverse events were considered unrelated to the vaccine’
Dr. Jessica Rose, viral immunologist and biologist, told the panel EUA of biological agents requires the existence of an emergency and the nonexistence of alternate treatment. ‘There is no emergency and COVID-19 is exceedingly treatable,’ Rose said.
In a peer-reviewed study19 co-authored by Rose, myocarditis rates were significantly higher in people 13 to 23 years old within eight weeks of the COVID vaccine rollout. In 12- to15-year-olds, Rose said, reported cases of myocarditis were 19 times higher than background rates …
Rose said tens of thousands of reports have been submitted to VAERS for children ages 0 to 18. Rose explained: ‘In this age group, 60 children have died — 23 of them were less than 2 years old. It is disturbing to note that ‘product administered to patient of inappropriate age’ was filed 5,510 times in this age group. Two children were inappropriately injected, presumably by a trained medical professional, and subsequently died.’”
During the meeting, Dr. Cody Meissner noted we don’t know whether the shot is safe for this age group, and the risk of COVID is extremely low. If the shot is authorized, mandates will likely follow, which would be “bad.”
Brownstone Institute is also objecting to the authorization. In an October 20, 2021, article,20 Paul Elias Alexander, Ph.D., a former assistant professor of evidence-based medicine and research methods, called the plan to vaccinate young children “absolutely reckless” and “dangerous based on lack of safety data and poor research methodology.”
Meanwhile, data show not a single child has died from COVID-19 who did not have a serious underlying health condition. Alexander reviews a lot of that data in his article.
Staggering Conflicts Of Interest
When you look at the roster of the FDA’s committee members21 who reviewed and voted to authorize the Pfizer shot for children as young as 5, the unanimous “yes” vote becomes less of a mystery. As reported by National File,22 they have staggering conflicts of interest. Members include:
- Gregg Sylvester — A former vice president of Pfizer Vaccines
- Arnold S. Monto — A paid Pfizer consultant
- Archana Chatterjee — A recent Pfizer research grant recipient
- Myron Levine — Mentor to Raphael Simon, senior director of vaccine research and development at Pfizer
- James Hidreth — President of Meharry Medical College, which administers Pfizer vaccines
- Geeta Swamy — Chair of the Independent Data Monitoring Committee for the Pfizer Group B Streptococcus Vaccine Program
- Steven Pergam — Proudly photographed taking a Pfizer vaccine
- Several people who are already on the record supporting coronavirus vaccines for children, including Ofer Levy, Jay Portnoy and Melinda Wharton
In addition to that, former FDA commissioner Scott Gottlieb is currently on Pfizer’s board of directors.
FDA Buries Data On Seriously Injured Children
With these shots now being pushed on young children, it’s more imperative than ever to understand how data are being massaged and manipulated to support the ongoing lunacy. Of particular concern is evidence that the U.S. Food and Drug Administration is burying data on children who were seriously injured in the vaccine trials. As reported by Aaron Siri on Substack:23
“Pfizer’s clinical trial for children aged 12-15 included only 1,131 children who were vaccinated and at least one of those children suffered a devastating, life-altering injury which, despite incontrovertible proof and the cries of both the victim and her parents, has not been appropriately acknowledged by Pfizer or the FDA.
Putting aside that one serious injury in a small trial should alone raise blaring alarm bells, one must ask: what other serious adverse events have been hidden and ignored by regulators?”
Siri tells the story of 12-year-old Maddie de Garay, who along with her two brothers were enrolled by her parents in Pfizer’s clinical trial. That decision has changed the lives of the entire family, possibly forever. Within 24 hours of her second dose, Maddie suffered crippling pain and systemic injuries.
Maddie is now wheelchair-bound and requires a feeding tube. Pfizer’s principal investigator initially claimed Maddie’s injuries were unrelated to the shot and treated her as a mental patient. Eventually, her injury was listed as “functional abdominal pain” in Pfizer’s report to the FDA.
“For a virus that rarely harms children, the need to assure safety of the Covid-19 vaccine is high. A study with only 1,131 children is underpowered. It will not pick up anything but the most common adverse events.
If what Maddie suffered will occur in 1/1,000 children, that would result in 75,000 children in this country suffering this serious injury. If it happens 1/10,000 children, that is 7,500 suffering this serious injury.
“It could be that the cure is worse than the disease. But that will only be known if there is a properly powered (a.k.a., sized) clinical trial with children,” Siri writes, adding that:
“International scientists have declared that ‘inadequately powered studies should themselves be considered a breach of ethical standards.’24 Without a clinical trial of sufficient size that reviews all potential adverse events, such as that experienced by Maddie, for a sufficient duration, this potentially catastrophic result will not be identified prior to authorization or licensure …
The real lesson is not that pharmaceutical companies, or the FDA should act better or do a better job. That just won’t always be the case. The real lesson is that civil and individual rights should never be contingent upon a medical procedure. Never.
Preserving those rights to choose whether to get a medical product, without any government coercion, is the final and ultimate safeguard.
Removing that right results in dangerous authoritarianism because just as the FDA will not admit to Maddie’s serious injury after having promoted this vaccine, politicians that mandate the vaccine will not want to later admit a mistake by repealing the mandate.”
FDA Sued To Access COVID Jab Trial Data
We’re now in a position where it’s near-impossible for many to refuse the COVID jab, and if injured, they cannot sue anyone for damages. Adding insult to injury, we don’t even have access to all the data governments are supposedly relying on to mandate these hazardous products.
To address this last point, an organization called Public Health and Medical Professionals for Transparency (PHMPT) is now suing25 the FDA after the agency refused to release the data on which it based its decision to approve Comirnaty.26
The FDA denied the PHMPT request for expedited processing of its Freedom of Information Act (FOIA) request on the basis that no “imminent threat to the life or physical safety of an individual” existed. Per the complaint:27
“… in an effort to ensure that the FDA acts in furtherance of its commitment to transparency, PHMPT seeks to obtain the data and information relied upon by the FDA to license the Pfizer Vaccine.
The importance of releasing to the public this information is also recognized under federal law which provides that: ‘After a license has been issued, the following data and information in the biological product file are immediately available for public disclosure unless extraordinary circumstances are shown: (1) All safety and effectiveness data and information. (2) A protocol for a test or study …’”
‘Just Say No’ To The COVID Shot
While U.S. authorities are doing their best to hide incriminating data and manipulating the rest to show some sort of benefit, common sense, medical facts and available data all point in the opposite direction. It’s crystal clear to me that children do not need the COVID shot, as their risk of serious COVID-19 infection and death is virtually nonexistent.
On the other hand, children are quite likely to be seriously injured by these injections. The reason you’re not getting the truth from the media is explained by Dr. Peter McCullough in the video above. In short, it’s a planned propaganda campaign — “the promotion of false information by the people in charge.”
According to McCullough, anyone under the age of 50 has a less than 1 percent chance of a bad outcome if they come down with COVID-19. “Why would you take the vaccine?” he asks. “My advice,” he says, “is just say no to this [shot], especially young people who are not at risk.”
Sources and References
- 1 The Bureau of Investigative Journalism February 23, 2021
- 2, 4, 5, 6 Public Citizen October 19, 2021
- 3 Twitter Zain Rizvi October 19, 2021
- 7 COVID19up.org August 17, 2021
- 8 SKirsch.io/vaccine-resources
- 9, 10 MedRxiv July 28, 2021
- 11, 12 Trends in Internal Medicine 2021; 1(1): 1-6 (PDF)
- 13, 15 CDC Morbidity and Mortality Weekly Report October 22, 2021: 70
- 14 Forbes October 22, 2021
- 16 ZeroHedge October 26, 2021
- 17 Twitter Techno Fog October 26, 2021
- 18 The Defender October 26, 2021
- 19 Curr. Probl. Cardiol. September 30, 2021; 101011
- 20 Brownstone Institute October 20, 2021
- 21 FDA Members Office of Vaccine Research and Review Meeting Roster
- 22 National File October 26, 2021
- 23 Aaronsiri.substack.com October 22, 2021
- 24 PLOS Medicine August 2008; 5(8): e172
- 25, 27 US District Court Northern District of Texas Case 4:21-cv-01058-P
- 26 Aaronsiri.substack.com October 11, 2021
Prominent Scientists Go Public: ‘Fauci Fooled America’
By Jeremy Loffredo | The Defender | November 2, 2021
In an op-ed, “Fauci Fooled America,” published Monday in Newsweek, two scientists accused Dr. Anthony Fauci of bungling the government’s response to COVID by getting “major epidemiology and public health questions wrong.”
Martin Kulldorff, Ph.D., an epidemiologist at Harvard Medical School, and Jay Bhattacharya, M.D., Ph.D., professor of Health Policy at Stanford University School of Medicine wrote: “Reality and scientific studies have now caught up with him.”
Kulldorff and Bhattacharya, both senior scholars at the Brownstone Institute and signers of the Great Barrington Declaration, had this message for Newsweek readers:
“The evidence is in. Governors, journalists, scientists, university presidents, hospital administrators and business leaders can continue to follow Dr. Anthony Fauci or open their eyes. After 700,000-plus COVID deaths and the devastating effects of lockdowns, it is time to return to basic principles of public health.”
The authors ticked off a list of “key issues” Fauci got wrong, including failure to recognize natural immunity, protecting the elderly, school closures, masks and contact tracing.
“By pushing vaccine mandates, Dr. Fauci ignores naturally acquired immunity among the COVID-recovered, of which there are more than 45 million in the United States,” the authors wrote. “Mounting evidence indicates that natural immunity is stronger and longer lasting than vaccine-induced immunity.”
Kulldorff and Bhattacharya cited a study from Israel, which concluded the vaccinated were 27 times more likely to get symptomatic COVID than the unvaccinated who had recovered from a prior infection.
They pointed out that the scientific community has known about natural immunity from disease “at least since the Athenian Plague in 430 BC.”
On Fauci’s dictates to mandate the vaccine for healthcare workers, the two argued: “Under Fauci’s mandates, hospitals are firing heroic nurses who recovered from COVID they contracted while caring for patients. With their superior immunity, they can safely care for the oldest and frailest patients with even lower transmission risk than the vaccinated.”
On school closures they wrote: “Considering the devastating effects of school closures on children, Dr. Fauci’s advocacy for school closures may be the single biggest mistake of his career … While children do get infected, their risk for COVID death is minuscule, lower than their already low risk of dying from the flu.”
Kulldorff and Bhattacharya pointed to Sweden, noting that during the 2020 spring wave of COVID, the country kept daycare and schools open for all 1.8 million children ages 1 to 15, with no masks, testing or social distancing.
According to the authors, Sweden’s strategy resulted in “zero COVID deaths among children and a COVID risk to teachers lower than the average of other professions.”
The authors argued contact tracing “was a hopeless waste of valuable public health resources that did not stop the disease,” and that Fauci failed at protecting the vulnerable.
“After more than 700,000 reported COVID deaths in America, we now know that lockdowns failed to protect high-risk older people,” they said.
On collateral public health damage, they argued that a “fundamental public health principle is that health is multidimensional; the control of a single infectious disease is not synonymous with health.”
They wrote that Fauci: “ … failed to properly consider and weigh the disastrous effects lockdowns would have on cancer detection and treatment, cardiovascular disease outcomes, diabetes care, childhood vaccination rates, mental health and opioid overdoses, to name a few. Americans will live with — and die from — this collateral damage for many years to come.”
In private conversations, Kulldorff and Bhattacharya said, most of their scientific colleagues agree with them on these points but few have spoken up out of fear of “financial censorship.”
“Many are afraid of losing positions or research grants, aware that Dr. Fauci sits on top of the largest pile of infectious disease research money in the world,” they wrote.
In his forthcoming book, “The Real Anthony Fauci,” Robert F. Kennedy, Jr. includes a comprehensive discussion of Fauci’s influence and power over the scientific community, revealing how Fauci uses the “financial clout at his disposal to wield extraordinary influence over hospitals, universities, journals and thousands of influential doctors and scientists — whose careers and institutions he has the power to ruin, advance or reward.” Kennedy’s book is due out Nov. 16.
Jeremy Loffredo is a freelance reporter for The Defender. His investigative reporting has been featured in The Grayzone and Unlimited Hangout. Jeremy formerly produced news programs at RT America.
© 2021 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.
Biden blames Russia & OPEC for high oil and gas prices in US
RT | November 3, 2021
President Joe Biden has called out Russia and OPEC countries for causing US energy prices to rise, even as he implements policies to curtail domestic oil and natural gas production.
“If you take a look at, you know, gas prices and you take a look at oil prices, that is a consequence of, thus far, the refusal of Russia or the OPEC nations to pump more oil,” Biden told reporters on Tuesday at the COP26 climate summit in Scotland. “We’ll see what happens on that score sooner than later,” he added.
Prices for the leading US crude benchmark, West Texas Intermediate (WTI), have surged to around $84 per barrel from $48 per barrel since the beginning of 2021, contributing to the nation’s highest inflation rate in 13 years. Gasoline prices are at a seven-year high. The key natural gas benchmark, Henry Hub, is nearing $6/mmBtu in Nymex futures trading after starting the year below $2.50/mmBtu.
While the president pointed the finger at Russia and OPEC for failing to help bring down oil prices, he said that inflation more broadly is being spurred by the Covid-19 pandemic’s impact on supply chains. US Transportation Secretary Pete Buttigieg said on Sunday that the supply-chain woes will continue until the pandemic ends.
The Biden administration called on OPEC in August to help bring oil prices down, raising the ire of major US producers, who argued that he should be encouraging higher domestic supplies.
The day he took office in January, Biden revoked a federal permit for a new pipeline needed to bring more Canadian oil to US refiners. A week later, he suspended the leasing of new oil and gas properties on federal lands and waters as part of his plan to slash reliance on fossil fuels.
The US surpassed Russia and Saudi Arabia as the world’s largest crude producer in 2018 and became the third-biggest exporter of liquefied natural gas in 2019. That same year, the country achieved net energy independence for the first time since the 1950s – reaching a goal that many observers thought impossible.
But US oil and gas output stumbled last year amid the Covid-19 pandemic, and domestic volumes are projected to decline again in 2021.
CDC Advisors Unanimously Endorse Pfizer’s COVID Vaccine for Kids 5-11 Despite Expert Concerns Over Clinical Data
By Megan Redshaw | The Defender | November 2, 2021
The Centers for Disease Control and Prevention’s (CDC) vaccine advisory panel today unanimously recommended Pfizer’s COVID vaccine for children 5 to 11, despite concerns raised during the meeting about Pfizer’s clinical data, the fact that children who previously acquired natural immunity to COVID were included in clinical trials and evidence showing COVID poses little risk to children.
If Dr. Rochelle Walensky, the CDC’s director signs off on the decision, children ages 5 through 11 could start receiving COVID vaccines as early as tonight.
The younger age group will receive one-third of the dose authorized for those 12 and older in two shots at least three weeks apart. The doses will be delivered by smaller needles and stored in smaller vials to avoid a mix-up with adult doses.
The CDC’s guidelines for the vaccine’s use are not legally binding, but heavily influence the medical community’s practice.
Prior to today’s decision by the CDC’s Advisory Committee on Immunization Practices (ACIP) the Biden administration enlisted more than 20,000 pediatricians, family doctors and pharmacies to administer the vaccines — with 15 million doses already packed with dry ice, loaded into small specialized containers and shipped via airplanes and trucks to vaccination sites across the country, federal officials said on Monday.
Walensky sent a clear signal during the ACIP meeting about where she stands, CNN reported. “We have been asking when we will be able to expand this protection to our younger children,” Walensky said in opening comments to the committee.
“As you review the data today, it will be key to keep in mind the specific risks to children from this virus and the pandemic, and to put that risk into context of other vaccine-preventable diseases,” Walensky said.
Walensky noted that children are routinely vaccinated against diseases like chickenpox — which results in far fewer hospitalizations and deaths in children compared to COVID.
During today’s meeting, ACIP members reviewed and discussed the science behind the U.S. Food and Drug Administration’s (FDA) authorization last week of Pfizer’s COVID vaccine in all children 5-11 years old.
That authorization was based mostly on a Pfizer-BioNTech study of 4,600 children worldwide, of whom approximately 3,100 got the low-dose vaccine and about 1,500 got a placebo.
These studies showed the vaccine is about 91% effective against COVID. The immune system response to the vaccine, as measured by antibodies, was comparable to the response seen in 16- to 25-year-olds, NPR reported.
During the meeting, the CDC said 745 children under 18 have died of COVID since the beginning of the pandemic — although the COVID-19 team admitted 79% were confirmed to be hospitalized for COVID, while the rest were hospital admissions for other causes.
“The chance that a child will have severe COVID, require hospitalization or develop a long-term complication like MIS-C [multisystem inflammatory syndrome] remains low, but still the risk is too high and too devastating to our children, and far higher than for many other diseases for which we vaccinate children,” Walensky said.
Efficacy of Pfizer’s COVID vaccine in children
The CDC said Pfizer’s COVID vaccine was 90.9% effective against symptomatic COVID and none of the adverse events experienced during clinical trials were assessed by “the investigator” as related to the vaccine.
To determine the efficacy of the Pfizer-BioNTech COVID vaccine, Pfizer measured the blood of 264 children for antibodies.
“There were 3,000 vaccinated children in the trial. Why isn’t blood from the other 2,700-plus being measured for antibodies?” asked Dr. Meryl Nass, a member of the Children’s Health Defense Scientific Advisory Panel.
“Pfizer never explains why, when they have an important clinical trial in which over 3,000 children were injected in this age group, only a subset of less than 10% were used to assess efficacy,” Nass said.
Nass explained:
“Pfizer claims three cases of COVID in the vaccinated group versus 16 in the placebo group show efficacy of the vaccine. But the FDA did not accept this claim. Note that all cases were mild, none hospitalized or died. So are they planning to vaccinate 28 million kids to prevent colds?”
Nass noted Pfizer also enrolled kids who had prior evidence of having had COVID in the clinical trial, “which should never have been allowed.”
“Of the kids who were already immune at the start of the trials, none developed COVID,” Nass said. “About 150 kids in the placebo group were recovered and none got COVID.”
Nass said kids with preceding COVID infection did not have their antibody levels checked after the first dose, as Pfizer stated they did not collect the data because they “tried to minimize blood draws in children.”
“The real reason they did not want to collect data is because it might support the fact that kids who already had COVID might only need one vaccine dose, or none at all,” Nass said.
During the brief public comment session, Patricia Neuenschwander, a registered nurse noted there was no prevention of hospitalization, death or multisystem inflammatory syndrome in children — a condition being used to justify vaccinating younger children against COVID, despite numerous cases of MIS-C having been reported after receipt of a COVID vaccine.
Neuenschwander reminded the ACIP that vaccinations do not prevent infection or transmission. It is a mild illness in the vast majority of children, she said, and prior immunity is being ignored — the expansion group was only followed for 17 days.
David Wiseman, a research scientist with a background in pharmacy, pharmacology and experimental pathology, asked the CDC panel why the efficacy study was not validated by the FDA, and why Pfizer changed the buffer [see page 14] in the vaccine but did not test it in animals or kids — planning to use an untested version of the vaccine in 5 to 11-year-olds.
Wiseman said the FDA abandoned its responsibility, and he asked if the ACIP would do the same.
Myocarditis and COVID in 5- to 11-year-olds
One side effect that generated considerable discussion at today’s meeting was myocarditis — a form of heart inflammation.
The CDC said 1,640 cases of myocarditis have been reported to the CDC’s Vaccine Adverse Event Reporting System in people under age 30 after having received a COVID vaccine, but only 877 met the CDC’s case definition.
The CDC said there were nine reported deaths in people with myocarditis, but then the agency reduced the number to three, with two cases pending evaluation and one case without adequate information.
“I have to say that it is beyond belief that CDC could whittle down 877 cases reported in young people to three actual cases. Where did the rest go?” Nass asked.
“According to the CDC’s Vaccine Safety Datalink, 7 of 16 12- to 17-year-olds with myocarditis were still on exercise restriction three months after diagnosis — that is 44% could not exercise three months later,” Nass said. “This is huge.”
Nass further noted 25% of 250 myocarditis cases were still symptomatic at three months, and only 74% of cases were designated by cardiologists as definitely resolved at 3 months.
As it pertains to safety, some who testified during a public comment period, as well as other commentators, questioned whether the study used by the FDA to grant Emergency Use Authorization is large enough to assure parents that the vaccine is safe in young children.
“The bottom line is getting COVID, I think, is much riskier to the heart than getting this vaccine,” said Dr. Matthew Oster, a pediatric cardiologist at Children’s Hospital of Atlanta.
Dr. Tom Shimabukuro covered vaccine safety monitoring from the CDC’s surveillance system in children. Shimabukuro said COVID is getting the “most intensive vaccine monitoring program in history,” yet he did not go into detail on surveillance data.
Acknowledging that some parents are hesitant about vaccinating their children right away, Dr. Matthew Daley, a member of the ACIP said, “we hear you loud and clear and of course you only want what’s best for your child. I encourage you to talk to your family physician or pediatrician, they can walk through this with you.”
Megan Redshaw is a freelance reporter for The Defender. She has a background in political science, a law degree and extensive training in natural health.
© 2021 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.
The EU is not revealing the details of its contracts with vaccine makers. Why?
By Robert Bridge | RT | November 3, 2021
As some Europeans continue to resist mandatory vaccine measures, a group of parliamentarians have upbraided the Commission for allowing pharmaceutical companies to ‘run roughshod over democracy.’
One of the most important lessons people learn early in life is to never plunk down hard-earned cash on a product before reading all of the fine print contained in the contract. ‘Caveat emptor,’ as every subject of the Roman Empire instinctively understood.
Yet, it seems that few bureaucrats in Brussels have purchased a new home, used car or some newfangled device lately, because that’s exactly what these bumbling fools have done. In an effort to ‘protect the health of their constituents,’ they bought millions of batches of Covid vaccines from various pharmaceutical companies without letting lawmakers sneak a peek at the contracts.
As it turns out, entire pages of these documents – the few that have been made public, that is – have been heavily redacted. This has raised more than one eyebrow in the European Union, and perhaps none more conspicuously than that of Romanian MEP Cristian Terhes.
At the weekend, Terhes appeared at a press conference in Brussels with several other EU lawmakers at this side, all visibly shaken by the news that they would be required to produce, starting on November 3, a digital ‘green pass’ to gain entry into Parliament. Like many EU citizens, these lawmakers have declined to get the vaccine not because they are ‘anti-vaxxers’ but because they have been denied critical information regarding the product and procedures. Now they will be refused entry into Parliament, the place where the will of their people is (supposedly) represented.
Terhes revealed that, back in January, EU lawmakers were demanding “full access to the contracts signed between these companies that produce the vaccines and the European Union.” To say the parliamentarians were disappointed would be a gross understatement.
The Romanian MEP, who represents the Christian-Democratic National Peasants Party, quoted from a Euractiv article that reported: “The contract, signed between pharmaceutical company CureVac and the European Commission in November, was made available to MEPs [on January 12, 2021] in a redacted format after the company agreed to open the contract up to scrutiny.”
That is really putting the cart before the horse, for how can something that has been so grossly redacted be opened up to scrutiny? Terhes railed that Brussels is “imposing a medical product on European citizens without them knowing what’s in these contracts.” That’s simply inexcusable and should be easily struck down by even a third-rate lawyer.
More astonishing is that not even the EU members of Parliament know the details of the agreements.
To prove his point, the Romanian MEP held up individual pages of the CureVac contract, each one heavily redacted like some kind of imitation of artist Kazimir Malevich’s ‘Black Square.’ It doesn’t get any less concerning when we drill down to which parts of the contract were blacked out. According to an analysis conducted by Euractiv, “4.22% of the liability section and 15.38% of the indemnification section was found to be redacted, while 0% of the section on the processing of personal data was redacted.”
Meanwhile, the contract’s annexes, which delve into the nitty-gritty details of the agreement, were redacted by some 61%. In total, almost 24% of the contract was hidden. Now ask yourself this simple question: Would you sign up for a home mortgage if it was discovered that one-quarter of the agreement was missing? I’ll crawl out on a limb and guess ‘no.’ Nor would anyone think you were ‘anti-mortgage’ or ‘mortgage hesitant’ if you did so.
The truth is that you, and millions of other rational people exactly like you, are simply ‘pro-transparency.’ Yet these medical consumers are being treated like second-class citizens for simply wanting more information before they agree to be injected with something. ‘My body, my choice’ is a battle cry that no longer applies, as millions of people are quickly discovering, in the current authoritarian climate.
Keep in mind that it is on the basis of these contracts that Europeans must come to a decision, based on “informed consent,” that they will ‘voluntarily’ take the jab so as not to be ostracized from polite society. Unless they agree to take one of the available vaccines, citizens of the EU face potentially being denied the right to work, enter a store, buy medicine, take their children to school and freely travel from one country to another.
Naturally, this makes the stakes for not taking the jab incredibly high, but that only makes it worse that details are being deliberately withheld from the public. It is no secret that the pharmaceutical giants enjoy full indemnity in the event that an individual suffers death or injury after receiving a Covid shot. And although such unfortunate occurrences appear to be rare, even Pfizer-BioNTech, which has been granted approval to extend vaccinations to 12 to 15-year-olds in the EU, seems uncertain as to what the long-term effects of the vaccines may be.
“Additional adverse reactions, some of which may be serious, may become apparent with more widespread use of the Pfizer-BioNTech Covid-19 Vaccine,” it clearly states on its website.
In February, the Bureau of Investigative Journalism released a damning report on Pfizer, saying negotiators for the drug company had behaved in a “bullying” manner with several Latin American countries. In Argentina they demanded “additional indemnity” against civilians seeking legal compensation after suffering adverse effects from their vaccines. In the agreements, Pfizer takes great care to ensure that all financial responsibility for compensating citizens injured from the inoculations is that of the respective government.
The company also enjoys the protection of non-disclosure agreements with many of its nation clients, including the European Commission and the US government. With regards to the EU, Brussels is forbidden from disclosing information that would be “material to Pfizer without the consent of Pfizer,” Public Citizen reported.
In fact, CureVac was being quite generous with the EU Commission, considering it was the only pharmaceutical company that agreed to release its contract to the light of day. Of course there wasn’t much to inspect with all of the redactions, but beggars can’t be choosers, right?
In light of the steady pressure bearing down on Brussels, much of it happening behind closed doors, the European Commission has obliquely admitted – almost one year too late, and after the rights and freedoms of European citizens have been crushed underfoot – that they failed to use good judgment when ramming through these emergency vaccines.
Last week, in an overwhelmingly passed resolution (458 in favor, 149 against and 86 abstaining), the EU Parliament demanded legislation that would make “the process of researching, purchasing and distributing Covid-19 vaccines more transparent, stating:
“This would enable MEPs to effectively scrutinize EU vaccine policies. At the same time, the Commission should be discussing these policies more openly with citizens.”
This shocking statement by the EU Parliament shows how little respect Brussels had for democratic principles when it was negotiating with the vaccine makers, who have, incidentally, reaped a windfall from the pandemic. The parliamentarians, who are coming under fire at home, demanded that “the Commission discloses who negotiates vaccine purchases on its behalf. It should publish purchase agreements made with vaccine suppliers, including details of public investments and vaccine costs, and publicise any potential breaches of contract.”
Then, in what comes off as the understatement of the century, the MEPs are of the opinion that “more information could help counter vaccine hesitancy and disinformation, and pharmaceutical companies should also release extensive clinical trial data and reports.”
Oh, you think so?
The following question is not an idle one: Why are MEPs ONLY NOW talking about the total lack of transparency and democracy that occurred between the EU Commission and Big Pharma? A more cynical person would be tempted to say it’s because the draconian vaccine mandates have finally reached the very door of Parliament, where the power brokers find themselves locked out of their offices, much like thousands of people on the street. Welcome to the club.
In any case, the fact that Brussels has withheld the details of its agreements with the vaccine makers for almost a year, while at the same time casually destroying the civil liberties of its citizens, totally disqualifies them from punishing those people who are ‘hesitant’ about receiving the vaccine. ‘Informed consent’ is essential to any functioning democracy, and Europeans were clearly denied that right. Do the right thing, Brussels, and release these heavy chains from your people. The world is watching.
Robert Bridge is an American writer and journalist. He is the author of ‘Midnight in the American Empire,’ How Corporations and Their Political Servants are Destroying the American Dream.















