Back in August of 2022, I wrote a piece on Pfizer’s Paxlovid approval. I talked about how the White House awarded Pfizer billions of taxpayer dollars before producing conclusive findings of safety or efficacy to the FDA.
In approving Paxlovid, the Biden White House and the FDA also seemed to deliberately ignore hundreds of clinical trials conducted on hundreds of thousands of patients detailing the established safety and efficacy of IVM and HCQ.
Like many other things the Biden White House implements, they force through a multitude of ideas, concepts and public health mandates which “seem” like they could work, but without the requisite conclusive scientifically obtained evidence that they will work.
On top of that, the White House doesn’t seem interested in learning. They repeat their mistakes in establishing America’s policies time and time again. Emergencies or not; there is no excuse for foregoing the scientific method (or using poor testing methodologies) thereby placing the Americans at risk – especially when it comes to public health.
Paxlovid is just one of dozens of examples of public health mendacity (too many to list here) pushed by the chaotic Biden White House and its ethically pliant partisan marionettes at the FDA. In the case of Paxlovid, not only was evidence of failure deliberately ignored; prospective testing methodologies were altered mid-trial to favor a positive outcome when it became apparent that the Paxlovid trial results would not meet their original endpoints. In fact, Pfizer had already opted to stop its Paxlovid trial, but then changed their minds after the FDA intervened via the White House.
Even worse: Its not the first time the FDA has forsaken science under Biden (I warned this would be a repeating theme in early 2021). Paxlovid was a failure, but the White House had foolishly already paid Pfizer $5.3 Billion in advance. Rather than admit failure and epic waste, the FDA then stepped in and with zero transparency, altered the established clinical trial parameters mid-trial to make Paxlovid’s findings seem better than they were. Pfizer then completed the trial, declared Paxlovid a success and the White House doubled-down on its $5.3 Billion investment, spending a sickening total of $10.6 Billion on Paxlovid.
That moral and scientific decision was approved by America’s insufferable, self-righteous taxpayer-funded civil servants who proclaim the left is “the party of science” and celebrated that when Biden was elected, “the adults are back in charge.”
“Following the science” is their tired jingle, but not their actual policy.
Even more outrageous were the number of nurses, pharmacists and physicians who witnessed – and fully recognized the scientific misconduct – but remained (and continue to remain) silent, inexplicably choosing to follow clinical recommendations from politicians, bureaucratic hospital administrators, mainstream news or social media. It is impossible to overstate the cowardliness, conformism and malpractice of these professionals in betraying their oaths to protect patients.
In reality, Americans still don’t have answers form the White House, FDA or any other HHS officials on:
1) The White House’s logic of purchasing $10.6 Billion of Paxlovid, and without concrete evidence of safety and effectiveness;
2) How many unused Paxlovid doses remain that will ultimately expire and be thrown away due to non-use, milder disease making it epidemiologically unnecessary;
3) Disclosure of the real-world incidence of “rebound” Paxlovid infections (which would be hard for drug safety epidemiologists to uncover because the White House, Pfizer and FDA have every reason in the world to under-report it, plus “rebound” is not an official [MedDRA] adverse event reporting term);
4) The current/historical prescribing and rates and other Paxlovid adverse event updates;
5) A full disclosure of communications with Pfizer, the White House and FDA officials with a scientifically legitimate explanation of why altered critical parameters of the Paxlovid were made mid-trial and in lieu of starting a completely new trial;
6) An official pharmacologic, mechanistic explanation of “Paxlovid rebound” ;
7) Why the Paxlovid trial was compared to placebo only, and had no IVM / HCQ / other comparator arms.
February 28, 2023
Posted by aletho |
Deception, Science and Pseudo-Science, Timeless or most popular, War Crimes | FDA, Joe Biden, United States |
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Data continues to emerge according to which not only were the mRNA shots ineffective at preventing infection and transmission of COVID-19, but they may have caused widespread harm to persons cajoled or coerced into undergoing vaccination, despite their own relative invulnerability to the worst effects of the virus. Anecdotal cases abound, but diehard regime narrative devotees continue to dismiss such “incidents”—thousands of which are recorded in the government’s own VAERS (Vaccine Adverse Effects Reporting System) database—as purely coincidental. It is more difficult to downplay reports involving entire cohorts, such as the increased incidence of myocarditis among young males, which the CDC itself has acknowledged. Some critics have suggested that a disproportionately high percentage of pregnant women in Pfizer’s initial trial of the shots suffered miscarriages.
Back in November 2021, in the midst of the widespread and aggressive “Vaccinate everyone!” campaign, I spoke with a woman in Oregon who matter-of-factly mentioned that her (vaccinated) daughter had suffered three recent miscarriages. Recognizing that it was too late to do anything anyway, given that the daughter had already been vaccinated, I did not dare to suggest that her troubles may have been caused by the shots she had no doubt been exhorted by her doctor to take. At that time, following the lead of CDC director Rochelle Walensky, health officials everywhere were in the midst of a marketing blitz according to which COVID-19 vaccination would protect mothers and their babies alike.
I said nothing to the woman in Oregon about the dangers of introducing foreign substances into pregnant women (although I had written about it), but I did naturally wonder at the time whether there might be a causal connection between the poor daughter’s miscarriages and the shots, given the biological activity of the spike protein already known to induce blood clotting and heart troubles. The mother of the young woman—who was pregnant again, for a fourth time—seemed optimistic that somehow there was nothing to worry about, even after three failed attempts to bring a baby into the world. It is possible, I realized then and continue to own, as I must, that the woman was simply unable, for unrelated reasons, to carry a child to term. But given that the biologically active spike protein is what the original virus used to access cells, and production of lots of it was induced by the injected mRNA, it would not take a tinfoil hat conspiracy theorist to surmise that the pregnancies may have been sabotaged by the shots.
Critics such as feminist scholar Naomi Wolf, who early on in the pandemic raised questions about the shot’s safety, given many reports of irregular menstrual cycles in women who under went vaccination, were denounced as purveyors of misinformation and immediately deplatformed by the social media giants. Only recently have such “conspiracy theorists” been permitted to articulate their concerns in the public sphere once again—and only on some platforms, including Twitter, which to Elon Musk’s credit reinstated thousands of accounts shut down for the crime of deviating from the narrative favored by the pharma-government alliance. If the shots are indeed dangerous to fetuses, it is needless to say too late for all of the pregnant women tricked into believing that because the CDC insisted that there was no evidence of risk to them and their offspring, they should therefore roll up their sleeves.
That Pfizer knew all along that their mRNA shots had effects upon women’s hormonal systems was corroborated through Project Veritas’ sting operation involving a Pfizer research director, Jordon Triston Walker. In the recorded interview thought by him to be a friendly conversation with a date, Walker observed that the shots seemed somehow to be affecting the endocrine systems of women. The delicate hormonal balance needed to maintain a pregnancy suggests an immediate connection between the widely reported menstruation irregularities of women and the incidence of miscarriages in some of the initial trial subjects.
The data interpreted by some critics to imply that miscarriage was one of the many possible side effects of the Pfizer shot were made public only recently, with the release of a large trove of court-ordered documents which the company is now required by law to provide, despite its initial insistence that it would take seventy-five years to do so. Setting aside the question of whether miscarriage is in fact a side effect of the shots, the very idea that it would take so many years to make public the documents said to have served as the basis for the FDA’s (Food and Drug Administration’s) decision to grant the Pfizer product Emergency Use Authorization (EUA), so that it could forego the customarily stringent multi-year testing program required of pharmaceutical products more generally, struck many people as absurd.
To my mind, the situation constituted a classic Charybdis and Scylla. If it was humanly impossible to process and assess all of the data (all 451,000 pages of it) in the short period between the creation of the vaccines and December 11, 2020, when the EUA was granted, this could be taken to imply that the persons on the committee incompetently executed their role and indeed based their decision to approve the shots primarily on Pfizer’s obvious wish that they do so. Alternatively, it was always possible to process the documents for publication, and the company’s resistance to doing so was due to the content of the documents themselves, which might harm the ambitious sales program to vaccinate everyone on the planet with the new product.
The director of the CDC, Rochelle Walensky, encouraged pregnant women from the beginning to get the shots, quite deceptively claiming that there was no cause for worry about possible health risks to fetuses. The safety information provided with the original shots itself indicated that pregnant women had been excluded from the initial trials, as they are for most pharmaceutical products. The reason why pregnant women are not included in early stage clinical trials of products intended for the general population is because they represent a special case, given the fragile chemical environment enveloping the fetus. It is a matter of common knowledge that developing human beings are highly sensitive to and often endangered by foreign substances—alcohol and nicotine being two well-documented examples. The vulnerability of fetuses was most notoriously and unforgettably demonstrated when pregnant women were prescribed Thalidomide on the basis of clinical trials which, again, excluded pregnant women. As in the case of the COVID-19 vaccines, Thalidomide was distributed by doctors under the misleading marketing line that there was no evidence that it would harm fetuses. Thalidomide killed thousands of babies and deformed thousands more before it was finally withdrawn from the market.
We now know from Pfizer safety data recently released that some of the women in the initial trial were in fact pregnant—apparently without having known that this was the case at the time, which was why they were not excluded from the trial. The vaccines may or may not have caused their reported miscarriages, but the fact that the CDC would encourage pregnant women, on the basis of nearly no data, to undergo vaccination betrays a reckless disregard and their true goals in injecting everyone everywhere, even members of low risk cohorts, with the mRNA treatment. Ignorance is bliss for pharmaceutical companies, which can continue to market and sell products for years, reaping billions of dollars of profits, before finally halting sales on the basis of widely reported and what come eventually to be undeniable post-launch problems, as in the cases of Vioxx, Belviq, Baycol, etc.
Above and beyond the profit motive was plausibly the desire to test the newfangled mRNA technology on the largest sample of human beings possible—whether or not they actually needed any treatment whatsoever in contending with COVID-19. Of course, if the desire on the part of Pfizer CEO Albert Bourla and Moderna CEO Stéphane Bancel was to make strides ahead in the research and development of other lucrative medications, then the quest for data, too, was ultimately driven by the profit motive—albeit looking forward, to future possible blockbuster drugs.
Certainly, the steadfast resistance, indeed, the outright refusal on the part of public health authorities such as Dr. Anthony Fauci and Dr. Rochelle Walensky, for more than a year after the launch of the COVID-19 vaccines, to acknowledge the relevance of natural immunity in those persons previously infected, and to recommend appropriate adjustments to the U.S. government’s mandates—for both health care workers and military personnel—supports the hypothesis that one of the overarching aims of the aggressive, relentless vaccine campaign was not to save the lives of the small percentage of human beings vulnerable to the virus, but to amass data.
Corroborating this interpretation, according to which the companies hoped not only to reap a windfall of profits but also to collect a huge amount of data, is the explanation by many critics (including Robert F. Kennedy, Jr. and Dr. Peter McCullough) of the assiduous suppression of any and every other therapeutic which the vaccine salespersons recognized would compete with and diminish the uptake of the newly patented products. Most importantly of all, ivermectin and hydroxychloroquine were dismissed and denounced by public health authorities, and ridiculed by parroting pundits throughout the media, because EUA cannot be granted to products when alternative therapies are available.
In his conversation with a Project Veritas reporter, Dr. Jordon Triston Walker also shared the potentially explosive piece of information that Pfizer executives had floated ideas such as mutating the COVID-19 virus so as to be able to develop vaccines preemptively. It was not entirely clear from Walker’s remarks whether the intention would be to release those mutated viruses so as to direct the course of the disease in populations, or simply to predict which variants would pop up on the scene naturally, through mutations of the virus in its effort to self-propagate by evading the antibodies induced by the latest shots.
Pfizer responded to the bombshell revelation by effectively minimizing the story through suggesting that the process described by their (now former, I presume) employee was essentially part of the normal, necessary research conducted in producing, for example, the flu shot each year. Nearly everyone by now is more or less aware that the flu shot is a gamble, involving researchers predicting which strains will be most prevalent and virulent. People who undergo inoculation against those versions may still fall ill because they may or may not come in contact with the predicted dominant strains. Some individuals report anecdotally that they were never more ill than during a year when they opted for the “free” flu shot, which clearly indicates that they encountered versions of the pathogen not expected by the researchers who determined the ingredients for the products distributed during that particular flu season. Unsurprisingly, neither anecdotal reports, nor adverse effects, nor even consistently poor efficacy rates have deterred pharmaceutical firms from pushing for widespread uptake of their mediocre flu shot products in very public and misleading advertising campaigns fronted by government health authorities.
Needless to say, if the intention of Pfizer in mutating the COVID-19 virus was to release it into the human population in order to induce countless numbers of persons to seek protection by purchasing (or obtaining from their government) the “vaccine” developed in order to stop that strain, then that would constitute a flagrant violation of any decent person’s basic sense of ethics. Such a possibility would moreover, and disconcertingly, be taken by some to accrue a degree of plausibility to the conspiratorial notion according to which the original COVID-19 virus was not only a gain-of-function product, created by researchers in a lab, but also intentionally released into the world in order to initiate The Great Reset being promoted by members of the World Economic Forum (WEF), led by Klaus Schwab.
More plausible, I believe, is that Pfizer and Moderna, et al., are primarily focused on the future of their other new mRNA products in the works. It is not at all far-fetched to surmise that the relentless, divisive push to vaccinate everyone everywhere with the first mRNA treatment ever tested on a population of human beings, made possible only by the FDA’s EUA, was spearheaded by companies with much broader goals in mind. The CEOs of these companies have publicly vaunted their plans to use mRNA to cure cancer and other intractable diseases, which in fact best explains their manifest fervor to acquire as much data as possible, by all means necessary. Such a program, albeit less explicitly heinous than creating illnesses in order to be able to sell patented cures for the symptoms caused by them, nonetheless involved using all of the people coerced into undergoing treatments for which they had no need as the means to the companies’ mercenary ends.
Further evidence for this admittedly unsavory interpretation can be seen in the push to vaccinate children, even infants, despite the minimal danger posed to them by the COVID-19 virus. If, in reality, the chances of a child dying from COVID-19 is less than the chance of their being hit by a bolt of lightning, then it is hard to see why anyone would push for uptake under a public health pretext. Yet those who wish to foist the product on young persons, including infants, have continued to press the line according to which the virus poses a serious health risk to everyone, and the vaccine will help to protect children along with their parents, this despite data according to which the protection provided by the shots, even to the vulnerable persons who might be said to benefit, plummets to nothing after only a few months. (Preposterously enough, according to one recent study at the Cleveland Clinic, in the longterm, the more shots one has received, the greater become one’s chances of contracting COVID-19!)
A second reason why children have been important for the product companies is peculiar to the United States, where the PREP Act (Public Readiness and Emergency Preparedness Act) protecting companies from liability in the event of adverse effects covers any product approved as a part of the child immunization schedule. Demonstrating their complete capture by pharmaceutical industry forces, on February 9, 2023, the CDC added the COVID-19 shots to the long list of those recommended in the childhood vaccination schedule (which now includes dozens of shots), thus ensuring the product companies massive profits for years to come through the inoculation of persons not at significant risk from the virus, using a product whose already nearly negligible protective capacity for invulnerable persons (a risk reduction of ~1%—or less) spans less than a few months.
Unbelievably enough, the new CDC recommendation for children (beginning at six months) includes the original COVID-19 vaccine, though the wild strain of the virus may no longer exist, along with booster shots, for which the only clinical trial on human beings is currently underway—on the millions of persons who rolled up their sleeves on the basis of safety data gathered from only animal trials. The results are trickling in on the first-round of “bivalent” booster shots, which have so far been demonstrated to have only middling (30%) efficacy in preventing infection by the variant they are attended to address. But the virus will continue to mutate, thus serving as the pretext for producing new booster formulas. This implies that, under the CDC’s immunization guidelines, each new booster shot will of necessity constitute yet another experimental trial, to be conducted, shockingly enough, upon children throughout the years of their development into adults. In other words, children have been set up to serve as test subjects (i.e., human guinea pigs) for each newly developed “booster” to follow in the future as the virus continues to mutate, despite the fact that they make up the least vulnerable cohort of them all.
Why should “vaccines” which do not offer longterm immunity to anyone and are not even necessary for children—the CDC itself explicitly claims that most children will experience only mild symptoms from COVID-19—be included in the battery of time-tested vaccines such as those against polio, measles, etc.? Along with the desire to sell products, and to be able to test new products on children, is, again, scandalously enough, the fact that the CDC’s addition of the mRNA shots to the children’s immunization schedule protects the manufacturers in perpetuity from lawsuits, even after the State of Emergency has ended. President Biden has announced that the State of Emergency will be lifted on May 11, 2023, two months after the CDC added the COVID-19 shots to the children’s immunization schedule.
Because state and local officials follow the cues of the CDC, we can expect to see its recommendation for childhood inoculation by the COVID-19 shots swiftly transformed into mandates for public school children in states throughout the country. This will likely happen in places such as Massachusetts, California, and New York, where health authorities have persisted in retaining laws which restrict the behavior of residents even as new data continues to refute the erroneous premises widely embraced by officials in the spring of 2020 regarding masks, social distancing, etc. Although states such as Florida rescinded the COVID-19 emergency laws, and have passed legislation to protect children, the fact remains: with the federal level CDC recommendation in place, the product companies will retain their protection from future litigation arising from adverse effects, even if the data currently being collected and analyzed eventually demonstrate widespread harm to either children or adults.
It would be a mistake to judge corporations by the moral standards appropriate to individual persons. Corporations are beholden only to their stockholders, and their sole goal is to maximize profit. But the spokespersons for such companies are themselves individual human beings, as are all of the authorities representing public health organizations whose ostensible raison d’être is to protect members of society, not to maximize the profits of their sponsors. When institutions such as the FDA are coopted by mercenary forces, they cease to perform the function which citizens are depending upon them to execute. Because this already happened in the case of the opioid crisis, the fact that people fell for the trick once again in the case of the COVID-19 “vaccines” is best and perhaps only explained by the fearmongering campaign used to psychologically traumatize them to the point where they lost all critical bearings and agreed to undergo an experimental treatment of which most of them had no need.
Every healthy, nonobese person under the age of seventy who underwent COVID-19 vaccination was deceived into serving as a pro bono experimental subject in a pharmaceutical product trial. That millions of well-meaning parents, believing that they are doing the right thing, will on the basis of the CDC’s addition of the COVID-19 shots to the children’s immunization schedule, enroll their progeny in an entire series of such experimental trials, using substances never before tested on human beings, is nothing less than tragic.
Laurie Calhoun is the author of We Kill Because We Can: From Soldiering to Assassination in the Drone Age, War and Delusion: A Critical Examination, Theodicy: A Metaphilosophical Investigation, You Can Leave, Laminated Souls, and Philosophy Unmasked: A Skeptic’s Critique, in addition to many essays and book chapters.
February 27, 2023
Posted by aletho |
Corruption, Deception, Science and Pseudo-Science, Timeless or most popular, War Crimes | Covid-19, COVID-19 Vaccine, FDA, Moderna, Pfizer, United States, WEF |
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The agency must have told some truths, but it’s hard to identify those statements.
Substack All-Star Igor Chudov just published another important article. This article asks if the CDC was lying all along about “vaccine effectiveness?”
My question (and it’s a serious one) is this: Can someone name ONE pronouncement of CDC officials that either wasn’t a lie or of highly-dubious veracity?
Per my assessment, the CDC and other national public health agencies and their key experts …
Lied about there being no evidence of early cases in America.
Lied when they said there was no possibility this virus leaked from a lab.
Lied about the effectiveness of masks.
Lied when they said the virus could be spread on physical surfaces.
Lied when they said it would take only two weeks to “flatten the curve.”
Lied when they said that virus transmission could easily happen outside.
Lied about the stats of “cases” and “deaths.”
Lied about the mortality risk to children and healthy young adults.
Lied about ivermectin and HCQ being worthless drugs for treatment.
Lied about remdesivir being a safe drug.
Lied about the vaccines being “safe and effective.”
Lied when they labeled these shots as “vaccines.”
Lied about the “vaccines” and boosters preventing “severe” cases and deaths.
Lied about the necessity or importance of testing people (including the asymptomatic) over and over.
Lied when they attacked and sought to censor people who were telling the truth.
Lied when they “adjusted” estimates of ILI in the Flu Season of 2019-2020 … to make it seem this flu season did not produce “widespread” and “severe” ILI (Covid?) outbreaks.
Before Covid, lied about the effectiveness of the flu vaccines.
Do liars continue to lie? Will liars lie again?
Do liars often try to cover-up their lies?
Do liars in positions of great power often attack people who try to expose their lies?
Is it smart to continue to trust proven or known liars?
How many lies does some person or agency have to tell before people start to realize they are listening to a liar?
February 27, 2023
Posted by aletho |
Deception, Science and Pseudo-Science, Timeless or most popular | CDC, Covid-19, COVID-19 Vaccine, United States |
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Author Ed Dowd joins ‘Tucker Carlson Today’ to discuss the ‘very large’ measurable increases in excess deaths across the Western world
https://www.foxnews.com/video/6321006774112
February 27, 2023
Posted by aletho |
Deception, Video, War Crimes | COVID-19 Vaccine, United States |
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Judicial Watch has filed a Freedom of Information Act (FOIA) lawsuit against the Department of Homeland Security (DHS) after the agency refused to provide records of communications related to election misinformation flagged by its Election Integrity Partnership (EIP).
Judicial Watch filed the lawsuit after another agency under the DHS, the Cybersecurity and Information Security Agency (CISA) failed to comply with an FOIA request filed last October.
We obtained a copy of the complaint for you here.
Judicial Watch had requested all communications related to EIP’s work sent via Atlassian’s Jira platform between employees and CISA employees and social media companies and other organizations that flagged election misinformation including The Center for Internet Security, the National Association of State Election Directors, and the Atlantic Council’s Digital Forensics Research Laboratory.
Numerous organizations privately communicated through Jira, according to the lawsuit.
“The Elon Musk ‘Twitter Files’ are the tip of the iceberg, as the federal government ran a massive, secret censorship op against the American people,” said Judicial Watch President Tom Fitton. “That the DHS is hiding these censorship records in violation of FOIA law shows the agency still has something to hide.”
In a separate lawsuit, Judicial Watch is suing the DHS for all communications between CISA and EIP, alleging that the agencies were actively flagging content in last year’s midterms. EIP flagged right-leaning news websites, including The Epoch Times, Breitbart, Fox News, The Washington Times, the New York Post, and Just the News.
February 26, 2023
Posted by aletho |
Civil Liberties, Deception, Full Spectrum Dominance | DHS, United States |
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Studies, trials by Pfizer Biontech were “seriously flawed” and fraught with “many irregularities” German journalist finds. It’s all beginning to dawn on the media…
Emergency approval based on sloppy and deceptive trials and studies?
At Germany’s flagship daily Die Welt, journalist Elke Bodderas recently penned an investigative article: The Many Irregularities In The Pfizer Approval Study
Until recently, Germany’s mainstream media had refused to report on the glaring number of side effects of the COVID 19 mRNA vaccines, dismissing them has disinformation spread by rightwing crackpots. But now there’s no denying something has gone terribly awry, and that the “crackpots” had been right all along.
Cover-up?
In her article, Bodderas concedes that the Biontech/Pfizer’s mRNA vaccine appears to have been “based on incorrect documentation”, that there is “growing doubt about the data from the pivotal Phase 3 trial” and that “Pfizer is dodging the accusations and refusing to be scrutinized.”
The metropolis Buenos Aires was a key area for test phase with almost 6000 of the 43,548 test subjects worldwide, and things there, according to Die Welt’s Bodderas, “did not go as they should have”.
The “significant, consequential irregularities” that arose during the trials “cast the entire study of the efficacy and side effects of the Biontech/Pfizer vaccine in a different light.”
No one believes “safe and effective”, not even the media
In Germany, the days of believing the new mRNA vaccines by Biontech and Pfizer are “safe and effective” are finally disappearing as a reluctant mainstream media begins to report on the glaring adverse effects and the now well-known inadequately conducted trials.
In other parts of the world, it’s been long known that these new experimental vaccines not only did not work like they once had been claimed to do, but that they also never prevented the transmission of the virus and had numerous, dangerous side effects. Only now, months later, are these now well-known facts beginning to dawn on Germany’s mainstream media.
Shoddily conducted trials
Die Welt reports on how Argentine test candidate Augusto Roux, a 36-year old lawyer, felt unwell after having received his second dose in the trials, then “experienced shortness of breath, burning chest pain, nausea, and fever” and that “his urine turned black like cola” before passing out. After having been admitted to a hospital, physician Gisela di Stilio suspected an “adverse reaction to coronavirus vaccine (high probability).” But Roux was simply dropped from the December 2020 study, and never appeared in subsequent evaluations. Instead he was counted as having suffered from COVID-19.
Suppression of unwelcome results?
In total, “In one fell swoop, the test administration [in Buenos Aires] had said goodbye to 53 subjects on August 31, 2020. The test candidates had been ‘unblinded.’” reports Die Welt’s Bodderas.
Die Welt adds: “A total of 302 subjects of the vaccine group were deleted from the study after the second vaccination and thus not included in the evaluation. 200 of them came from Buenos Aires. Have unwelcome results been suppressed here?”
According to Bodderas, “Deaths were concealed, serious side effects were not registered, and the study protocol was violated several times.”
“The case casts a bad light on Pfizer, a company that has often been plagued by scandal in the past, but also on the regulatory agencies EMA and FDA.”
Bodderas also appeared on Bild’s Viertel Nach Acht: “Serious Flaws in Pfizer BioNTech Vaccine Study.”
February 26, 2023
Posted by aletho |
Deception, Science and Pseudo-Science, Timeless or most popular | COVID-19 Vaccine, EMA, FDA, Germany, Pfizer |
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I have used the trick of trying to think like the enemy and it has been a successful strategy for me. So here are a few thoughts to help focus on what might come and what the other side might be up to, but what might also stand in their way.
I’d be thrilled that my psychological warfare worked so well on a huge chunk of people. At first, anyway. I’d be wondering if it would work again.
I’d be worried that at least half the population (mostly blue collar) is no longer completely brainwashed. They are silent, but they are not buying the narrative. Only 15% got that bivalent booster.
I would not give a d**m about nation states (except for destroying them and diluting their people and cultures) and I would have no allegiance to any jurisdiction.
I would be a bit nervous about what those other globalists are doing, messing with MY air, water and soil.
I’d be very mad that Fauci and his buds promised me a deadly pandemic and it didn’t really make the cut, and now it is so mild no one is frightened of it any more.
I’d be mad that the same crowd promised me a severe monkeypox pandemic, and that didn’t work out so well, either. I can’t really trust them to get me the types of pandemics I wanted, can I?
I’d be nervous about how the people will respond to the next one that Bill Gates promised would be coming soon. They might just go after us for creating it and unleashing it. How do Bill Gates or Jeff Bezos ever show their face in public? I don’t want to be unable to go wherever I please.
I’d be nervous about the fact the COVID shots started killing people off too soon—too many people have figured it out, and getting them to take another shot is not going to be easy. This could be a huge problem, since the plan seems to have entailed giving everyone ten shots.
The vaccine passport plan failed, since the vaccines didn’t protect and Americans won’t go for it now. While we may be able to install them in some European countries, the plan was to get everyone to pay for their own tracker and control system. Now people are starting to ditch their phones, or keep them in Faraday bags. And the population is getting wary of politicians and public health officials.
We could pull out all the stops and kill or maim the majority of the population, but when people understand what’s happening, and they have nothing left to lose by fighting, they fight back. And we don’t have enough police and armies on our side to control them yet. We don’t have robot armies yet, either.
Will we dare to keep destroying food storage and production facilities? Won’t we make a mistake and it could be traced back to us?
How much can we squeeze the public over energy before they take matters into their own hands?
Our hardware infrastructure, till it is up on satellites, is vulnerable. But once it’s up on satellites, how do we fix it when it breaks? What if we kill off all the competent tech guys, almost all of whom in the US and Israel took the shots?
Small cells (5G) are easy to knock down. Tractors can knock down towers. I can build underground, but I don’t want to have to live in an underground bunker.
We can sink economies everywhere, whenever we choose. But if we starve enough people, there will be too many people with nothing left to lose.
What happens when the people find out who we are?
No one better start using any nukes on MY planet.
What happens when the people decide the governments aren’t legitimate because of the vote scams, and they turn off the money spigot? Do you expect me to spend my own billions on this world takeover? Fuggedaboudit.
____________________________
Thanks to the commenter who identified this piece in Brownstone: Technocratic Dystopia Is Impossible by Robert Blumen. His thesis is that it is physically not possible for elites to produce the desired utopia/dystopia. He mentions various descriptors of the dystopia below. Worth a read of his whole piece.
The WEF – an infinite source of technocratic malapropisms – says that you will “own nothing” and be happy (the happiness perhaps will be a drug-induced state as Yuval Hariri suggests). Many independent researchers who have looked into the WEF’s plans have reported similar findings. For example – see James Corbett, Patrick Wood, Whitney Webb 2, Tessa Lena 2, Jay Dyer, and Catherine Austin Fitts.
Aaron Kheriaty, who says much the same in his book The New Abnormal, calls the oncoming system “communist capitalism.” Jeffrey Tucker calls it “techno-primitivism.”
February 26, 2023
Posted by aletho |
Civil Liberties, Deception, Malthusian Ideology, Phony Scarcity, Supremacism, Social Darwinism, Timeless or most popular, War Crimes | COVID-19 Vaccine, Human rights, United States |
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Hobbled US Turns to War to Preserve its Waning Primacy
The future of humanity will be decided on a battlefield in Ukraine. That’s no exaggeration. The conflict between the United States and Russia will determine whether global economic integration will expand within an evolving multi-polar system or if the “rules-based order” will succeed in crushing any opponent to its Western-centric model. This is what’s taking place in Ukraine today, in fact, all of the recent government-prepared documents related to national security identify Russia and China as the greatest threats to US hegemony. For example, take a look at this brief clip from the 2021 Congressional Research Service Report titled Renewed Great Power Competition: Implications for Defense—Issues for Congress:
The U.S. goal of preventing the emergence of regional hegemons in Eurasia… is a policy choice reflecting two judgments: (1) that given the amount of people, resources, and economic activity in Eurasia, a regional hegemon in Eurasia would represent a concentration of power large enough to be able to threaten vital U.S. interests….
From a U.S. perspective on grand strategy and geopolitics, it can be noted that most of the world’s people, resources, and economic activity are located not in the Western Hemisphere, but in the other hemisphere, particularly Eurasia. In response to this basic feature of world geography, U.S. policymakers for the last several decades have chosen to pursue, as a key element of U.S. national strategy, a goal of preventing the emergence of regional hegemons in Eurasia.” (“Renewed Great Power Competition: Implications for Defense—Issues for Congress”, US Congress)
That sums up US foreign policy in a nutshell; “prevent the emergence of a regional hegemon” at all cost. Now check out this summary of the 2022 US National Defense Strategy by Andre Damon at the World Socialist Web Site :
These documents, which were not seriously discussed in the US media, make clear the fundamental falsehood that the massive US military buildup this year is a response to “Russian aggression.” In reality, in the thinking of the White House and Pentagon war planners, the massive increases in military spending and plans for war with China are created by “dramatic changes in geopolitics, technology, economics, and our environment.”
These documents make clear that the United States sees the economic rise of China as an existential threat, to be responded to with the threat of military force. The United States sees the subjugation of Russia as a critical stepping stone toward the conflict with China.” (“Pentagon national strategy document targets China”, Andre Damon, World Socialist Web Site )
These two excerpts are by no means a comprehensive summary of US foreign policy objectives, but they are a pretty effective thumbnail sketch. Bottom line: The war in Ukraine is not about Ukraine. America’s clearly articulated strategic objectives are as follows: To weaken Russia, topple its leader, take control of its vast natural resources and move on to containing China. Simply put, Washington’s escalating aggression in Ukraine is a Hail Mary pass aimed at containing emerging centers of economic power in order to preserve its waning position in the global order.
This is the geopolitical chess match that is being played behind the cover of “a war against Russia’s unprovoked aggression.” People should not be hoodwinked by that absurd deception. This war was concocted as a desperate attempt for the United States to defend its flickering global hegemony. That’s what Ukraine is really all about. It’s a clash between the warmongering western oligarchs who have a stranglehold on the US media and political establishment and the emerging economies that are using the market system to link their resources and manufactured goods to countries around the world through “high-speed” infrastructure and cooperative development.
So, the question everyone must ask themselves is this: Do you want to see more economic integration, lower prices, more shared prosperity and less war or another 80 years of onerous and arbitrary sanctions, color-coded revolutions, regime change operations, genocidal interventions and bioweapon warfare (Covid-19)? Which do you want?
Perhaps, you are one of the millions of Americans who believe that China is an enemy of the United States. Perhaps, you are also unaware of the role the US played in creating modern China. Here’s a question for you: Did the US and western corporations move their operations en masse to China to escape the high costs of production in the US?
answer– Yes, they did.
And, did they betray US workers because they didn’t want a fair wage to interfere with their excessive profit-making?
answer– Yep.
And, did they offshore their businesses, outsource their product manufacturing and do everything in their power to make themselves winners while robbing American workers of the opportunity of making a decent wage so they could put food on the table?
answer– They sure did.
Then who is actually responsible for the rise of China?
answer– Western corporations are responsible. If Americans want to blame someone, blame them!
But now the corporate mandarins and other elites are unhappy with China because China will not allow them to take control over their markets, financial system and currency as they have in America. So now these same cutthroat corporations want us to fight a war with the monster that they created?
Can you see that? Can you see that the relentless provocations against China have nothing to do with US national security or US interests. We are being led by the nose to fight and die for the cadres of voracious western oligarchs who have settled on China as the next target of their grand looting operation.
But let’s forget the past for a minute and focus on the future, after all, that’s what really matters, right?
Well then, which country has a more “positive vision” for the future: China or the United States?
Have you ever heard of China’s Belt and Road Initiative, the massive, multi trillion-dollar infrastructure plan that is the centerpiece of China’s foreign policy? It is the biggest infrastructure program in history and more 150 countries have invested in the plan already. It is a development-oriented project aimed at increasing connectivity through high-speed rail, shipping lanes and ports, skyscrapers, railroads, roads, bridges, airports, dams, power stations, and railroad tunnels. By increasing the speed of travel, China’s products and merchandise will get to markets faster generating greater prosperity for itself and for the other countries involved. And, keep in mind, the BRI will link countries around the world in a high-speed system that will not require its participants to follow a specific economic model dictated by Beijing. In other words, the Belt and Road Initiative is free market economics without the politics. It’s a “win-win” situation for everyone, a guarantee of mutual prosperity absent political manipulation, coercion or exploitation.
The venal oligarchs that run the US can’t even imagine a project of this scale or potential. In fact, they can’t even pony-up enough money to keep the trains on the rails in America. The profits these billionaire parasites extract from their activities invariably come from stock buybacks, tax evasion, and other sleight-of-hand, debt-layering ponzi-scams that benefit no one and merely shift more of the nation’s wealth into their own bulging bank accounts. Of course, ripping off the country would be bad enough, but now we see how this same class of miscreants have settled on public health as a means for amplifying their political power so they can impose repressive, police-state measures that greatly curtail the freedom of the entire population. In short, they want absolute social control and they aren’t going to let-up until they get it.
Where is the “positive vision” in this behavior?
There isn’t one. America used to be a country of ideas, ideals and vision. Now it is an oligarch-run detension center in which all hope for the future has been ruthlessly extinguished by a handful of mercenary billionaires.
At least, in the case of China, we can imagine a better, more prosperous world that is interconnected and more accessible to everyone. But what about the United States? Are we supposed to believe that fighting a war in eastern Europe is going to improve our lives? Are we supposed to believe that the only way “we can stay on top” is by pushing everyone else down? Are we expected to hate China and Russia even while our own government demonizes 80 million of us for voting for the wrong presidential candidate or for not supporting the terrorists who burn and loot our cities or for believing that the people in East Palestine are more deserving of our support and assistance than the Nazi stormtroopers in Kiev?
The fact is, our leaders cannot imagine devoting public resources to a giant interconnected infrastructure project like BRI, because that would mean less lucre for themselves. So, they’ve decided to destroy it just like they destroyed Nord Stream. Just read the press reviews on this groundbreaking project. Western journalists can’t find a ‘good word’ to say about it. A vast area in the center of America was fiendishly nuked with vinyl chloride, butyl acrylate and isobutylene, but the western media would rather criticize China’s ambitious BRI project than hold their paymasters accountable. Go figure.
The same rule applies to Russia. The Biden team and their wealthy allies don’t want closer relations between Germany and Russia because closer relations mean more prosperity for both countries, and Washington can’t have that, which is why they blew up the pipeline that was Germany’s lifeline to cheap fuel. That’s how Washington solved the problem. It pushed Germany and Russia down so the US could remain on top. Who doesn’t see this?
In contrast, the Belt and Road Initiative provides a positive vision for the future, which is an idea that the majority of the world supports. It puts us on a path to an interconnected world in which people can raise their standards of living, make a meaningful contribution to their communities, and enjoy their own culture and traditions without fear of being sanctioned, incarcerated or bombed to death. This is an excerpt from China’s Global Times :
The China-proposed Belt and Road Initiative (BRI) has already become a well-received international public good and an important platform for international cooperation…
“BRI transcends the outdated mentality of geopolitical games, and created a new model of international cooperation. It is not an exclusive group that excludes other participants but an open and inclusive cooperation platform. It is not just China’s solo effort, but a symphony performed by all participating countries….
Since the Belt and Road Initiative (BRI) was proposed in 2013, the initiative has always been development-oriented, and consistent efforts have been made to ensure that it is high-standard, sustainable and people-centered….
By August, China’s goods trade with countries participating in the BRI had reached around $12 trillion and the country’s non-financial direct investment in those countries surpassed $140 billion. … By the end of 2021, Chinese enterprises had invested $43 billion in the construction of economic and trade cooperation zones in BRI countries, creating more than 340,000 local jobs, official data showed…
China is open to other countries’ and regions’ participation in the BRI and is considering connecting with infrastructure initiatives proposed by other nations to provide more good-quality public goods for the world…. China hopes to join hands with all partners to advance the high-quality development … stressing that China aims to strive for global connection rather than fragmentation, for mutual opening-up rather than shutting doors, for mutual integration rather than zero-sum games. (“BRI remains open, inclusive for all, transcends the outdated mentality of geopolitical games“, Global Times )
What is the American-led project that rivals the Belt and Road Initiative?
There isn’t one. The US allocates over $1 trillion per year for lethal weaponry and war-making, and trillions more to bail out the Wall Street banksters, and trillions more to shut down all the businesses across the country that were forced to comply with the diktats of billionaire elites who wanted to inject the population with their toxic slurry, but zero for any global infrastructure project that would peacefully bring the world’s people closer together through commerce and recreation.
No one is saying that China is perfect, at least, I’m not. Nor do I want to live in China. I don’t. I’m an American and I plan to die here.
But I’m not blind. It’s easy to see that this war with Russia has nothing to do with “unprovoked aggression.” That is merely a smokescreen that’s being used to conceal the real objective, which is to preserve America’s global hegemony. What we need to do now, is honestly analyze ‘what is happening’; try to understand ‘why it is happening’, and, then, figure out what the outcome will be if the United States prevails. In other words, do we want to perpetuate an oligarch-controlled system that crushes Russia, contains China, starves Europe of the energy it needs, sabotages the Belt and Road infrastructure plan and reinforces the same failed policies that brought us Afghanistan, Libya, Syria and Iraq?
Do we want that? Do YOU want that?
The American people want their government to cooperate with other nations in order to create a more prosperous and peaceful world. They don’t want a new world order and they certainly don’t want a Third World War.
February 26, 2023
Posted by aletho |
Deception, Economics, Militarism | China, United States |
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In an interview with CNBC News in September 2020, Dr. Albert Bourla, the veterinarian Chief Executive Officer of Pfizer — the second largest pharmaceutical company in the world by revenue — said that anyone refusing to take the BioNTech vaccine will become “the weak link that will allow the virus to replicate”, and assured the public that “we will develop our product, develop our vaccine using the highest ethical standards”.
It was a dangerous claim to make, even for a CEO and investor making billions out of the experimental mRNA gene therapy product. Pfizer has a long history of paying out vast sums in out-of-court settlements to avoid not only claims in civil cases but also prosecution on criminal charges resulting from the fraudulent promotion, unapproved prescription and injury, including death, from use of its products. It has also offered millions in payments to doctors and scientists to prescribe, test, approve and recommend them to the public. So let’s have a look at what Dr. Albert Bourla means by Pfizer’s ‘ethical standards’.
- In 1992, Pfizer agreed to pay between $165 million and $215 million to settle lawsuits arising from the fracturing of the Bjork-Shiley Convexo-Concave heart valve, which by 2012 has resulted in 663 deaths.
- In 1996, Pfizer conducted an unapproved clinical trial on 200 Nigerian children with its experimental anti-meningitis drug, Trovafloxacin, without the consent of their parents and which led to the death of 11 children from kidney failure and left dozens more disabled. In 2011, Pfizer paid just $700,000 to four families who had lost a child and set up a $35 million fund for the disabled. This cover-up was the basis of the John Le Carré book and film The Constant Gardener.
- In 2004, Pfizer’s subsidiary Warner-Lambert was fined $430 million to resolve criminal charges and civil liabilities for the fraudulent promotion of its epilepsy drug, Neurontin, paying doctors to prescribe it for uses not approved by the Food and Drug Administration.
- In 2009, Pfizer spent $25.8 million lobbying Congressional lawmakers and federal agencies like the Department of Health and Human Services. Its expenditure on federal lobbying between 2006 and 2014 came to $89.89 million. In 2019 it spent $11 million lobbying the federal Government.
- In 2009, Pfizer set a record for the largest health care fraud settlement and the largest criminal fine of any kind, paying $2.3 billion to avoid criminal and civil liability for fraudulently marketing its anti-inflammatory drug, Bextra, which had been refused approval by the FDA due to safety concerns.
- In 2009, Pfizer paid $750 million to settle 35,000 claims that its diabetes drug, Rezulin, was responsible for 63 deaths and dozens of liver failures. In 1999, a senior epidemiologist at the Food and Drug Administration warned that Rezulin was “one of the most dangerous drugs on the market”.
- In 2010, Pfizer was ordered to pay $142.1 million in damages for violating a federal anti-racketeering law by its fraudulent sale and marketing of Neurontin for uses not approved by the FDA, including for migraines and bi-polar disorder.
- In 2010, Pfizer admitted that, in the last six months of 2009 alone, it had paid $20 million to 4,500 doctors in the U.S. for consulting and speaking on its behalf, and $15.3 million to 250 academic medical centres for clinical trials.
- In 2012, Pfizer paid $45 million to settle charges of bribing doctors and other health-care professionals employed by foreign Governments in order to win business. The Chief of the Securities and Exchange Commission Enforcement Division’s Foreign Corrupt Practices Act Unit said: “Pfizer subsidiaries in several countries had bribery so entwined in their sales culture that they offered points and bonus programs to improperly reward foreign officials who proved to be their best customers.”
- By 2012, Pfizer had paid $1.226 billion to settle claims by nearly 10,000 women that its hormone replacement therapy drug, Prempro, caused breast cancer.
- In 2013, Pfizer agreed to pay $55 million to settle criminal charges of failing to warn patients and doctors about the risks of kidney disease, kidney injury, kidney failure and acute interstitial nephritis caused by its proton pump inhibitor, Protonix.
- In 2013, Pfizer set aside $288 million to settle claims by 2,700 people that its smoking cessation drug, Chantix, caused suicidal thoughts and severe psychological disorders. The Food and Drug Administration subsequently determined that Chantix is probably associated with a higher risk of heart attack.
- In 2013, Pfizer absolved itself of claims that its antidepressant, Effexor, caused congenital heart defects in the children of pregnant woman by arguing that the prescribing obstetrician was responsible for advising the patient about the medication’s use.
- In 2014, Pfizer paid a further $325 million to settle a lawsuit brought by health-care benefit providers who claimed the company marketed its epilepsy drug, Neurontin, for purposes unapproved by the FDA.
- In 2014, Pfizer paid $35 million to settle a law suit accusing its subsidiary of promoting the kidney transplant drug, Rapamune, for unapproved uses, including bribing doctors to prescribe it to patients.
- In 2016, Pfizer was fined a record £84.2 million for overcharging the NHS for its rebranded and deregulated anti-epilepsy drug Phenytoin by 2,600% (from £2.83 to £67.50 a capsule), increasing the cost to U.K. taxpayers from £2 million in 2012 to about £50 million in 2013.
- In May 2018, Pfizer still had 6,000 lawsuits pending against claims that its testosterone replacement therapy products cause strokes, heart attacks, pulmonary embolism and deep vein thrombosis, and were fraudulently marketed at healthy men for uses not approved by the FDA.
- In June-August 2020, the U.S. Securities and Exchange Commission and the Department of Justice said they were looking at Pfizer’s activities in China and Russia under the Foreign Corrupt Practices Act, which forbids U.S. firms from bribing foreign officials.
- In November 2021, the British Medical Journal revealed that the Ventavia Research Group had falsified data, unblinded patients, employed inadequately trained vaccinators, and was slow to follow up on adverse events reported in the phase 3 trial for Pfizer’s ‘vaccine’.
- Since 2000, Pfizer has incurred $10.268 billion in penalties, including $5.637 billion for safety-related offences; $3.373 billion for unapproved promotion of medical products; $1.148 billion for government contract-related offences; $60 million under the Foreign Corrupt Practices Act; and $34.7 million for ‘kickbacks and bribery’.
Given this record of ongoing corruption and malpractice from, which only its enormous profits have saved it from criminal prosecution by means of out-of-court settlements, it seems extraordinary that Pfizer Inc. is still permitted to manufacture and sell any health-care products. Yet this is the pharmaceutical company we were asked by the U.K. Government, the Scientific Advisory Group for Emergencies, the Joint Committee on Vaccination and Immunisation, the U.K. Health Security Agency and the National Health Service to trust with the mass vaccination of 68 million people with a product that was rushed through clinical trials in seven months, employing experimental mRNA biotechnology whose clinical trials are not due to be completed until March 2023, for a disease with the infection fatality rate not much above seasonal influenza, which statistically is no threat to those under 50 years old, and for which there is no evidence that it prevents infection by the virus.
That was three years ago, during which the British people have paid with their freedoms, their health and their lives for believing the lies of their Government, their National Health Service and international pharmaceutical companies. Subsequent retractions by Pfizer, however, are an opportunity to revisit its claims in more detail.
On December 10th 2020, the U.S. Vaccines and Related Biological Products Advisory Committee met to evaluate the trial data on the efficacy and safety of Pfizer/BioNTech’s mRNA COVID-19 vaccine contained in the briefing document produced by Pfizer itself titled ‘Pfizer-BioNTech COVID-19 Vaccine (BNT162, PF-07302048) Vaccines and Related Biological Products Advisory Committee Briefing Document‘. It was on the basis of this evaluation that, on December 11th, the Food and Drug Administration (FDA) granted Emergency Use Authorisation to its mRNA gene therapy product. And given the subsequent debate about what Pfizer claimed its ‘vaccine’ would do, it might be useful to review the contents of this document.
The FDA’s Emergency Use Authorisation, which requires less data than standard approvals and is based on a lower standard of proof, was issued for a vaccine “intended to prevent Coronavirus Disease 2019 (COVID-19) caused by SARS-CoV-2”. It was issued for prevention, therefore, not for reduction of the severity of symptoms, as was claimed when it became clear the gene therapy product did not prevent infection. Pfizer’s claim was that its product had a ‘vaccine efficacy’ of 95% protection against COVID-19 occurring after second days from injection with the second dose. In its clinical trials, a ‘case’ of COVID-19 was defined as a positive RT-PCR test for SARS-CoV-2 and the presence of at least one of the following symptoms: fever, cough, shortness of breath, chills, muscle pain, loss of taste or smell, sore throat, diarrhoea or vomiting. Nothing was said about asymptomatic ‘cases’ of COVID-19, or claimed about the ability of the gene therapy product to stop ‘asymptomatic transmission’ of the virus.
Pfizer’s benefit assessment was that its mRNA vaccine may be able to induce “herd immunity”, induces strong “immune responses”, and “confers strong protection against COVID-19”. This clearly indicates protection against both infection with the virus and the disease. Since transmission of a virus from person to person requires prior infection, Pfizer’s claim that its vaccine protects against infection, and the suggestion that sufficient injections will induce ‘herd immunity’, is also, by extension, a claim that it stops transmission from the injected.
The subsequent claim by Janine Small, Pfizer’s President of International Developed Markets, during her testimony before the European Union Parliament in October 2022, that Pfizer never tested whether its ‘vaccine’ stopped transmission appears, therefore, to rest on the myth of ‘asymptomatic transmission’. The implication of her statement was that Pfizer’s product only stops infection with SARS-CoV-2 and symptoms of COVID-19. However, the FDA’s Emergency Use Authorisation for Pfizer’s vaccine was based on prevention of both infection and disease. Pfizer’s claim is not evidence, as many afterwards claimed, for the lack of justification for making injection a condition of lifting lockdown or imposing vaccine passports, but rather an attempt to deny responsibility for the failure of its product (from which it has made $69 billion) to meet either of its claims.
An indication of just how unscientific was the FDA’s Emergency Use Authorisation of Pfizer’s vaccine is that it was granted on the basis of protection from infection and disease, while conceding there is no evidence that the vaccine “prevents transmission from person to person“. This is the way the ‘Science’ we mustn’t question or deny but blindly follow is conducted in what I call the global biosecurity state. Indeed, three years after it announced the pandemic in March 2020, the World Health Organisation can still only offer the following justifications for the four vaccines authorised for use in the U.K.
- Pfizer/BioNTech: “There is modest vaccine impact on transmission.”
- AstraZeneca/Oxford: “No substantive data are available related to impact of the vaccine on transmission or viral shedding.”
- Moderna: “There is only modest impact on preventing mild infections and transmission.”
- Novavax: “There is not currently sufficient evidence to date to evaluate the impact of the vaccine on transmission.” (See World Health Organisation, ‘COVID-19 advice for the public: Getting vaccinated’.)
Failure to offer protection against infection or transmission, however, are the least of the failings of Pfizer’s ‘vaccine’. As the evidence of the harms and deaths caused by this experimental gene therapy product injected into the U.K. public becomes too overwhelming for all but the Covid-faithful, the British press, the U.K. Parliament and our Government to ignore, there have been no end of doctors, nurses and medical professionals protesting they thought Pfizer’s biotechnology was ‘safe and effective’. But aren’t they trained to spot when something is going medically very wrong?
As of January 25th 2023, the Medicines and Healthcare Products Regulatory Agency, responsible for authorising the injection of the Pfizer/BioNTech vaccine into U.K. citizens, has received 180,005 reports of 517,779 adverse reactions to the injections, over 70% of which reports (127,405) have been classified as ‘serious’, including 884 deaths following injection. Including AstraZeneca’s viral-vector gene therapy product and Moderna’s mRNA gene therapy, the MHRA has received a total of 477,553 reports of 1,555,433 adverse reactions to the COVID-19 gene therapies, 74 per cent of which (355,052 reports) are categorised as ‘serious’, including 2,436 deaths following injection.
By the MHRA’s own estimation, only 10% of serious adverse reactions and 2-4% of non-serious reactions are reported, so the actual tally of injuries, autoimmune disease, reproductive and breast disorders, miscarriages and premature births, facial paralysis, blood clotting, amputations, myocarditis, pericarditis, heart attacks and deaths — all of which were recorded in Pfizer’s own analysis of post-authorisation adverse events as early as February 2021 — is far higher, undoubtedly many times higher. Indeed, this — and not the risible excuses with which the U.K. public has been fobbed off by the U.K. media — is likely a major cause of the huge increase in mortality in the U.K. since the ‘vaccine’ programme was implemented, contributing to the more than 60,000 excess deaths in 2022.
Given which, it is my contention that any medical professional that authorised or administered the injection of U.K. citizens with the Pfizer/BioNTech gene therapy product is at risk of being found guilty in a court of law for failure to give sufficient warning of adverse effects and obtain informed consent.
Simon Elmer is the author of two new volumes of articles on the U.K. biosecurity state, Virtue and Terror and The New Normal, which are available in hardback, paperback and as an ebook. This article is an extract from an article in Volume 2, ‘Bowling for Pfizer’. Please click on these links for the contents page and purchase options. On March 11th, to mark the third anniversary since the declaration of the pandemic by the World Health Organisation, he will be holding a book launch at the Star & Garter, 62 Poland Street, W1F 7NX, upstairs in the William Blake room from 6-8pm. Entry is free, with book signings, a reading and open-mic discussion.
February 25, 2023
Posted by aletho |
Corruption, Deception, Science and Pseudo-Science, Timeless or most popular, War Crimes | COVID-19 Vaccine, FDA, Pfizer, UK |
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The Counter Measures Injury Compensation Program (CICP) is a string of words most Americans have never heard of. A program described as a ‘black hole’ where people disappear alternatively called ‘the payer of last resort.’
Its existence, and its negligence, is the biggest story left to be told throughout the failed Covid response. A ‘safety net’ only activated during emergencies to compensate Americans for injuries and deaths experienced from the use of countermeasures such as vaccines and anti-virals.
A broken promise of transparency from federal agencies during a rushed vaccine development and rollout sans any real semblance of safety testing gave way to a billion-dollar full-court pressure campaign from every conceivable angle. Get the shots in arms at any cost, double down on mistakes along the way was the unofficial motto of agencies like the CDC and FDA.
“Take the shot” commanded Biden through his trademark whisper and distressed face struggling to read his loaded teleprompter.
262,908,216 million Americans have walked blindly into another medical experiment unlikely to ever have full knowledge or informed consent to the medical procedure they agreed to.
Their only redress is at the mercy of an admittedly antiquated Vaccine Adverse Event Reporting System (VAERS) well-known for over a decade to vastly underreport true injuries and deaths from vaccination. In fact, HHS has known from an analysis by Harvard Pilgrim that less than 1% of adverse events occurring after vaccination are reported to VAERS.
The statute of limitations to file an injury or death claim is one year for CICP. Harms from the vaccines are still being discovered years after the first shot went into an American arm. Doesn’t matter in the CICP. Another barrier to claim fulfillment is stated on HRSA’s website:
“Temporal association between the administration or use of the covered countermeasure and onset of the injury (i.e., the injury occurs a certain time after the administration or use) is not sufficient, by itself, to prove that an injury is the direct result of a covered countermeasure.”
You read that right. Having an injury after the shot isn’t enough. What other obstacle is one up against when filing a claim? Aaron Siri, lead lawyer for the Informed Consent Action Network told Reuters :
“The CICP is not a court,” he said, noting that it’s part of the “same federal health department that licensed, recommended, and mandated Covid-19 vaccines, and then sits as an investigator and ‘judge’ of any CICP claim. That is a mockery of the term justice.”
Simply put, it’s a place you don’t want to find yourself. You versus the government – no courts, no public attention, and no transparency. Up against the very same well-funded bureaucratic apparatus that has only doubled down on warp-speeding shots into bodies as the science to justify it evaporates and the safety signal compound.
Now let’s investigate CICP’s funding. Keep in mind that a total of $11 trillion has been distributed in the form of federal spending, tax cuts, loans, grants, and subsidies authorized in the wake of the coronavirus pandemic and economic crisis. A Freedom of Information Act Request (FOIA) from author and researcher Wayne Rohde uncovered these numbers regarding CICP’s funding:
A total of $20M was set aside for claim compensation and budget when it was all said and done for the fiscal year 2023 or 0.00018% of government spending during the failed COVID response. For an unproven product rushed through safety testing and aggressively targeting, often through unconstitutional mandates, every adult, adolescent, child, and infant.
Rohde’s FOIA also uncovered that the CICP estimated that the allotted $15M would “be used to initiate the review of an estimated 1,500 medical reviews of claims and provide compensation to eligible individuals for injuries and deaths directly resulting from the use of covered countermeasures.” In other words, they expected 1,500 injury claims. What did they actually receive?
The latest update from the U.S. Health Resources & Services Administration, which administers the CICP, shows the following numbers:
Expected 1,500 claims…received 11,196…in an underreported system. Yet that’s not the most shocking piece of information. For nearly 3 years, HRSA has paid out zero claims. Not a penny to Covid vaccine-injured Americans waiting for assistance.
To get an idea of the potential backlog we are talking about, we go to VAERS where the first records of possible vaccine injuries are recorded before potentially moving onto a CICP claim. Here are the most recent number and types of reports filed after Covid shots:
From past behavior and current trajectory, the U.S. government will try at all costs to avoid taking accountability, financially, ethically, and legally, for the vast amounts and types of injuries caused by the rushed Covid shots. It is up to the media, politicians, and people everywhere to keep this story front and center in an effort to seek justice for those harmed.
February 25, 2023
Posted by aletho |
Civil Liberties, Deception | COVID-19 Vaccine, United States |
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