Shortly before Christmas, the 14 day Covid-19 infection incidence in Iceland by vaccination status started to change dramatically as the new omicron variant of the coronavirus began to gain the upper hand. By the end of the year, the 14-day incidence of infection among double-vaccinated people had increased sevenfold and was now double that of the unvaccinated, while increasing elevenfold for those with three jabs.
This information, published on the official Covid-19 information site run by the Directorate of Health, began tocirculate at the start of this year and attracted quite some attention. On January 7th, data updates on the website were temporarily halted, explained by planned restructuring of the site. The next day I published an article in Iceland‘s main newspaper, Morgunblaðið, drawing attention to this sudden change in the infection rates. Chief Epidemologist Þórólfur Guðnason responded the same day, quoting a systematic error in the numbers; many who were registered as living in Iceland did not actually live in the country, had been vaccinated abroad but were registered unvaccinated locally. Therefore, he claimed it was not possible to draw the conclusions the data clearly supported, that the double-vaccinated were more likely to become infected than the unvaccinated.
As I pointed out in another article in Morgunblaðið on January 11th, in order for his explanation to be correct, the Chief Epidemologist would have had to previously overestimate the number of unvaccinated people by 90% to get an infection rate equal to the rate for the double-vaccinated. As I explained, such a huge overestimation would hardly go undetected for over half a year.

Change in 14-day incidence of infections for unvaccinated, original vs. updated values
It was finally on the morning of January 13th that the data appeared again. However, there was a snag: While the 14-day incidence of double- and triple-vaccinated adults and children was virtually unchanged, for the unvaccinated, the previously published numbers had taken an unexplained jump, starting on December 27 with a 4% increase, 11% the next day, then 12%, 14%, 15% and ending in a 20% increase on January 4th!
What might justify such a huge and sudden change in previously published data? Either a large group of unvaccinated people would have had to disappear without a trace during the second half of December, or a large number of infections, all among the unvaccinated, would have had to be lost and then found again. But no such explanations have been made.
This sudden and significant change in official data took place immediately after the data started to show a development that was in direct contradiction to the Chief Epidemologist‘s repeated claims that the vaccines were highly effective for preventing infections. Is this a mistake, or is there a different explanation? This is something the Directorate of Health will have to answer.
January 21, 2022
Posted by aletho |
Deception, Science and Pseudo-Science | COVID-19 Vaccine, Iceland |
Leave a comment
In a January interview on Del Bigtree’s “The Highwire” —“COVID-19: Following the Money” — policy analyst A.J. DePriest, a member of the grassroots Tennessee Liberty Network, shared the group’s jaw-dropping findings about the undue influence of federal relief monies on school and hospital policies.
In this article, The Defender covers how federal money affected schools. We will cover the impact of federal money on hospitals in a separate article to follow.
In 2020 and 2021, Congress passed trillions in COVID-related stimulus through the Coronavirus Aid, Relief and Economic Security (CARES) Act, the Coronavirus Response and Relief Supplemental Appropriations (CRRSA) Act and the American Rescue Plan (ARP) Act.
Sizeable portions of those funds went to schools.
Digging into the education allotment, the Tennessee network discovered public, charter and nonprofit private schools in the U.S. received nearly $190.5 billion during three rounds of Elementary and Secondary School Emergency Relief (ESSER) funding (called ESSER I, II and III).
One of DePriest’s disquieting take-home messages is that this education lucre came with major strings attached — federal strings that are persuading ignominious school board members to adopt policies unfavorable and even dangerous to student health and well-being.
While DePriest characterized the stimulus bonanza as a “BIG carrot” for cash-strapped schools, that assessment may be too generous. If one examines the disturbing conditions attached to the U.S. Department of Education’s (DOE’s) dazzling largesse, the government billions seem closer to a godfather-like “offer they can’t refuse.”
The $190 billion ‘carrot’
The size of the federal “carrot” increased with each ESSER iteration. The $1.9 trillion ARP package alone assigned state educational agencies and school districts a whopping $122 billion (ESSER III).
On Jan. 18, the U.S. Department of Education (DOE) crowed about its disbursement of the final chunk of ESSER III monies, claiming the funds were “critical” for addressing “recent challenges” such as the putative and much-ballyhooed Omicron variant.
In Tennessee, the state’s initial take from ESSER I was nearly $260 million, but ESSER II quadrupled that amount to over $1.1 billion. By ESSER III, Tennessee’s educational haul had reached almost $2.5 billion.
The school district encompassing Memphis received roughly three-quarters of a billion dollars, DePriest noted, while Nashville schools pocketed a cool half a billion.
Schools and COVID vaccines
In DePriest’s view, there’s a catch that explains why school boards in every state have been so coldly unresponsive to parental pleas to unmask their children and abandon other COVID restrictions.
The catch is that federal generosity for state educational agencies is contingent on states proving to DOE (in reports submitted twice a year through fall 2023) they are meeting requirements synced with the Centers for Disease Control and Prevention’s (CDC’s) “safety recommendations.”
The CDC’s aggressive “recommendations” include:
- Enforcing “universal and correct wearing of masks”
- Physically modifying schools to facilitate “distancing”
- Ensuring “respiratory etiquette” and handwashing (likely with carcinogenic sanitizers)
- Implementing strenuous cleaning protocols to maintain “healthy facilities”
- Facilitating contact tracing, “in combination with isolation and quarantine”
- Conducting testing (both screening and diagnosis), helped along by additional resources from a federal-CDC-Rockefeller Foundation partnership to “ensure that all schools can access and set up screening testing programs as quickly as possible”
- Coordinating with state and local health officials
- Engaging in “efforts to provide vaccinations to school communities”
In its Jan. 18 press release, DOE took pains to emphasize that expanding access to vaccinations is “critical” for “safely reopening schools and sustaining safe operations.” And it furnished two ominous illustrations of how its stimulus monies are supporting vaccination efforts on the ground.
First, DOE noted, the Vermont Agency of Education is partnering with other statewide agencies “to vaccinate all Vermonters, including eligible students.” DOE approvingly stated that three-fourths of 12- to 17-year-olds in Vermont already received at least one dose.
DOE also considered the Hawaii Department of Education’s hosting of dozens of vaccination clinics for students, staff and “school communities” to be exemplary.
Further evidence of the feds’ hold over schools comes from the fact that some school districts have already taken steps to mandate COVID shots for some or all K-12 students, even in advance of formal U.S. Food and Drug Administration (FDA) approval.
Weaponizing HVAC systems?
More than 40% of school districts plan to spend some of their ESSER funds on “improvements” to heating, ventilation and air conditioning (HVAC) systems.
This raises a potential red flag in light of the Environmental Protection Agency’s (EPA) authorization in February 2021 — through a slippery “Public Health Emergency Exemption” — of a potentially hazardous, nanoparticle-based “air treatment” called Grignard Pure.
Dispersal of the chemical, authorized for indoor use in public spaces, occurs primarily “in-duct” via HVAC systems.
EPA’s authorization allows for Grignard Pure’s use in indoor spaces “when adherence to current public health guidelines … is impractical or difficult to maintain.”
As examples of spaces where the chemical’s use is permitted, the agency lists government facilities, healthcare facilities, food processing facilities and public transit.
EPA’s definition of “government facilities” does not appear to include schools, but the agency does admit to studying use of “air treatment technologies” on school buses.
A senior EPA scientist conceded last August, “how safe [the technologies] are, particularly for sensitive populations such as children, is not fully understood.” Given the experimental use of “air treatments” on school buses, it would behoove parents to query schools’ motives for upgrading their HVAC systems.
Moreover, though EPA initially green-lighted Grignard Pure in just two states (Georgia and Tennessee), it added four more states — Maryland, Nevada, Pennsylvania and Texas — last July.
The manufacturer’s website indicates that applications for Public Health Emergency Exemption are pending in another 15 states.
Nor does EPA’s vaguely worded list of indoor spaces seem to preclude use of the chemical in facilities not on that list. For example, Grignard Pure’s CEO is openly publicizing his product’s use in religious spaces, and a member of the company’s engineering steering committee elatedly stated last year, “There’s no limit to where we can use it!”
St. Simons Presbyterian Church in Georgia paved the way for church use, with the facility’s HVAC vents, which “run the length of both sides of the sanctuary’s ceiling,” apparently having been deemed ideal for spritzing congregants during services. This generates “a light haze [that] comes from the air vents and settles over the sanctuary.”
According to news accounts, the Georgia church’s pastor views Grignard Pure as “an added layer of safety,” a fact that the church emphasizes in its weekly bulletins. The pastor also is considering using the chemical-dispensing system during flu season.
Health risks associated with triethylene glycol
As The Defender previously reported, Grignard Pure’s supposedly virus-killing active ingredient is triethylene glycol (TEG), a chemical whose prior claim to fame was its use in theatrical fog machines.
Shortly before EPA reached its upbeat decision to approve TEG, the UK’s Scientific Advisory Group for Emergencies (SAGE) recommended against TEG’s use as a virucide due to its limited effectiveness and “potential health effects for those exposed over a long period of time.”
After WWII and in the early 1950s, there was an attempt to deploy TEG for “air disinfection” purposes in school settings. However, “wartime and post-war authors would not have had access to much of the toxicological and health data now available for this chemical,” said the UK SAGE group.
These data show “a number of potential acute health effects,” including respiratory tract irritation in case of inhalation.
A Berkeley, California lab — the Indoor Air Quality Scientific Findings Resource Bank — recently expressed multiple concerns about TEG in relation to air disinfection.
The indoor air quality experts cautioned, “careful attention should be given to dosage of triethylene glycol in indoor settings in order to minimize potential health effects caused by chemical exposure,” particularly in light of evidence of health effects with repeated exposure.
The Berkeley group also warned “TEG could react with other indoor chemicals” — including common disinfectants — “leading to additional and perhaps unexpected adverse health effects,” including toxic effects on human airway epithelial cells.
In light of these “uncertainties about TEG dosing, chemical mixtures, and health risks,” they suggested TEG should be viewed as a “lower priority” option.
In similar comments about the use of TEG “or other similar chemicals” for air disinfection (p. 23), SAGE wrote in November 2020:
“There is currently no strong evidence that using a continuous spray chemical in the air will be an effective control against SARS-CoV-2 transmission. … [T]here is no precedent for such an approach to be used as a continuous spray in an occupied space for infection control. Cleaning the air by spraying it with a chemical is a misnomer – it is simply swapping one contaminant for another.”
TEG’s cousin polyethylene glycol (PEG)
As The Defender reported a year ago, TEG is a chemical cousin to and sometime-component of polyethylene glycol (PEG), a synthetic, nondegradable polymer of questionable biocompatibility.
PEG is known to be associated with adverse immune responses, including anaphylaxis.
Both the Pfizer and Moderna COVID jabs use PEG to make their mRNA “carrier systems” work, and the compound is also present in numerous other drugs and consumer products.
Up to 72% of the U.S. population may have anti-PEG antibodies — including an estimated 8% with highly elevated levels — that could lead to life-threatening anaphylactic reactions. Research is needed to assess potential TEG-PEG cross-reactivity.
Children’s Health Defense (CHD) in August 2020 first sounded the alarm about the risks of PEG in COVID shots, pointing out that well before COVID, PEG had already been flagged, including by Moderna itself, for its potential to trigger immediate hypersensitivity reactions.
CHD was so concerned about the potential for anaphylaxis that it followed up with a letter to the FDA on Sept. 25, 2020, outlining the need for critical safeguards for Moderna clinical trial participants.
Those concerns have since been borne out by repeated reports of PEG-linked anaphylaxis that began surfacing concurrent with the two mRNA vaccines’ rollout.
Resistance is NOT futile
In mid-August, Tennessee’s governor issued an executive order giving parents ultimate decision-making authority over their children’s masking behavior at school.
U.S. Secretary of Education Miguel Cardona evinced no compunction about immediately chastising the governor and his education commissioner for taking matters into their own hands.
In a letter dated two days later, Cardona wrote that the Tennessee governor’s action was “at odds with the school district planning process embodied in the U.S. Department of Education’s. . . interim final requirements,” pointedly adding that CDC safety recommendations include “universal and correct wearing of masks.”
Meanwhile, Treasury Secretary Janet Yellen warned Arizona Gov. Doug Ducey on Jan. 14 that the Biden administration is prepared to take back Arizona’s relief funds — and also withhold future federal aid — due to the state’s active discouragement of school mask mandates.
Yellen offered no explanation as to why the Treasury Department, rather than DOE, was issuing the warning.
In response, Ducey emphasized Arizona’s focus on “things that matter” — math, not masks. Attorney General Mark Brnovich urged Yellen to rescind the threat, arguing that Treasury is “trying to overstep its constitutional bounds” by dictating how the state should run and fund its schools.
These types of intimidation tactics are also evident at the school-district level, prompting parents’ growing frustration.
Rather than continue to beg for mask lenience, DePriest reminds parents they have every right to confront school board members about the feds’ cash-in-exchange-for-obedience arrangements.
“They’re getting the money to mask your kids. It has nothing to do with health and safety,” DePriest said.
As evidenced by the quadrupling of homeschooling since the beginning of COVID, many families have simply had it. However, for parents for whom homeschooling is not an option, there is every reason to push local school boards to address their student-unfriendly behavior more transparently.
Here are a handful of possible questions and actions:
- Borrowing DePriest’s no-nonsense wording, a first step is to ask, “How much money are you taking from the federal government to commit this egregious, tyrannical behavior on our kids?” If school board members profess not to know, prepared citizens can easily present them with the financial information listed here.
- As one state describes it, “The governance of local school boards by democratically-elected individuals remains at the heart of two vital United States structures: the public education system and democracy itself.” Remind school board members that when they put politics and financial arm-twisting ahead of their relationship with the public and the students they are supposed to serve, they are engaging in a fundamental betrayal of trust and ethics.
- Emphasize to school board members that the damage caused by COVID restrictions has far outweighed any threat from the illness, turning schools into “a physically, spiritually, and emotionally unsafe place” for children. Moreover, none of the restrictions are genuinely evidence-based.
- Continue to present school board members with evidence about the experimental COVID injections’ dangers (see sample talking points here).
- Ask schools whether they are planning for or engaging in HVAC “improvements.” If yes, ask them to describe the purpose of the “improvements” and whether schools intend to use HVAC systems to disseminate unsafe chemicals. Tell them EPA is doing research on “air treatments” in school buses, and let them know about the risks — both known and hypothesized — of chemicals like TEG.
- Finally, for officials who claim that their hands are tied, A.J. DePriest has a ready solution: Tell them to “give the money back”!
© 2022 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.
January 21, 2022
Posted by aletho |
Civil Liberties, Science and Pseudo-Science | Covid-19, Human rights, United States |
Leave a comment
Here is an Announcement from the American Academy of Pediatrics website (May 4, 2021):
“Children ages 2-11 could potentially be eligible for (the still-experimental) COVID-19 vaccine this fall. Pfizer Chairman and CEO Albert Bourla, D.V.M., Ph.D. (Doctor of Veterinary Medicine), said on a quarterly earnings call Tuesday he expects to request (experimental) Emergency Use Authorization (EUA) from the Food and Drug Administration (FDA) in September. Under his plan, an EUA request for ages six months to 2 years would follow in the fourth quarter.
“Pfizer and its partner BioNTech currently are waiting for an FDA decision on an EUA for adolescents ages 12-15 years.”
And here is a list of lawsuits related to sixteen Pfizer drugs that were FDA-approved before long-term safety studies were completed:
(And the CDC Wonders Why There is Such a Thing as “Big Pharma/Big Vaccine-hesitancy”)
List Collated by Gary G. Kohls, MD – March 10, 2021 – (1041 words)
Pfizer is one of the largest multinational drug companies on the planet – and one of the five largest vaccine manufacturers (the other four are Sanofi, Merck, GlaxoSmithKline and Johnson $ Johnson. AstraZeneca is # 10). Pfizer has faced thousands of lawsuits for fraudulent marketing and medical injuries caused by some of its most profitable, drugs.
Pfizer has also set a record for the largest fine paid for a health care fraud lawsuit filed by the U.S. Department of Justice. Pfizer paid $2.3 billion in fines, penalties, and settlement for illegal marketing claims.
Here is a partial list of 13 of Pfizer’s most dangerous, most litigated, most potentially lethal drugs. (NOTE: If any reader had adverse effects to any of the following Pfizer drugs, he/she might want to consult an attorney).
Celebrex,
Bextra,
Geodon,
Zyvox,
Lyrica,
Neurontin,
Protonix,
Prempro,
Chantix,
Depo-Testosterone,
Zoloft,
Effexor,
Feldene,
Viagra,
Lipitor,
Zithromax,
Etc.
Celebrex and Bextra
Prizer promoted its two COX-2 pain relievers Celebrex and Bextra which generated 7000 lawsuits and a $894 million settlement. Both medications were me-too drugs similar to Merck’s infamous Vioxx, which caused 50,000 lawsuits because of cardiovascular deaths and injuries. Merck settled most of the cases with a $4.85 billion settlement.
Geodon, Zyvox, and Lyrica
Pfizer paid $1 billion to resolve allegations under the civil False Claims Act that the company illegally promoted four drugs – Bextra; Geodon, an anti-psychotic drug; Zyvox, an antibiotic; and Lyrica, an anti-epileptic drug – and caused false claims to be submitted to government health care programs for uses that were not medically accepted indications.
Neurontin
Pfizer paid out $142 million for committing racketeering fraud in the marketing of Neurontin.
Protonix
As part of a larger group of proton pump inhibitor lawsuits, Pfizer faced a number of Protonix lawsuits after it acquired drug company Wyeth who had been accused of marketing the drug for unapproved uses. In 2013, Pfizer agreed to pay $55 million to settle illegal marketing claims but the company may still be facing lawsuits for kidney injuries caused by the medication.
Prempro
Nearly 10,000 Prempro lawsuits were filed by women who had been diagnosed with breast cancer. The lawsuits were largely settled by 2012 for about $1 billion.
Chantix
Pfizer faced about 3,000 Chantix lawsuits filed by people who claimed they experienced suicidal thoughts and psychiatric disorders after using Chantix for smoking cessation. Pfizer set aside about $288 million and at least some of the cases were settled.
Depo-Testosterone
Thousands of cases of medical injury due to testosterone replacement therapy have been filed. Other drug companies have paid $ billions to settle their cases, however some Pfizer testosterone lawsuits were dismissed.
Zoloft
About 250 Zoloft lawsuits were filed, claiming Pfizer actively promoted the use of Zoloft to pregnant women despite knowledge of birth defect risks from their research. These cases were largely dismissed in 2016 when a judge concluded that there was not enough evidence to prove a link between birth defects and Zoloft use.
Effexor
Effexor was a medication originally produced by Wyeth which has also been the cause of multiple lawsuits. People who filed Effexor lawsuits claimed that it caused birth defects, and separately, suicidal thoughts and behaviors. In September 2015, Effexor lawsuits were dismissed but may have been eligible to refile.
Lipitor
Pfizer’s drug that lowers cholesterol (but only minimally decreases heart attack risk) but causes serious muscle damage, diabetes and other unforeseen health defects has generated billions of dollars of lawsuits.
Xeljanz
Pfizer’s arthritis and ulcerative colitis drug was only belatedly acknowledged by Pfizer to cause cancer, serious cardiovascular events and venous thromboembolism (such as pulmonary embolism or deep vein thrombosis). Many lawsuits are in progress.
Feldene; Viagra, Zithromax, etc
____________________________________________________________________________________________________________________________
Environmental Pollution
In 1971 the Environmental Protection Agency (EPA) asked Pfizer to end its long-time practice of dumping industrial wastes from its plant in Groton, Connecticut in the Long Island Sound. The company was reported to be disposing of about 1 million gallons of waste each year by that method.
In 1991 Pfizer agreed to pay $3.1 million to settle EPA charges that the company seriously damaged the Delaware River by failing to install pollution-control equipment at one of its plants in Pennsylvania.
In 1994 Pfizer agreed to pay $1.5 million as part of a consent decree with the EPA in connection with its dumping at a toxic waste site in Rhode Island.
In 1998 Pfizer agreed to pay a civil penalty of $625,000 for environmental violations discovered at its research facilities in Groton, Connecticut.
In 2002 New Jersey fined Pfizer $538,000 for failing to properly monitor wastewater discharged from its plant in Parsippany.
In 2003, shortly after Pfizer acquired Pharmacia, the company (along with Monsanto) agreed to pay some $700 million to settle a lawsuit over the dumping of known-to-be-carcinogenic PCBs in Anniston, Alabama.
In 2005 Pfizer agreed to pay $22,500 to settle EPA claims that the company failed to properly notify state and federal officials of a 2002 chemical release from its plant in Groton that seriously injured several employees and necessitated a major emergency response.
Also in 2005, Pfizer agreed to pay $46,250 to settle charges that its Pharmacia & Upjohn operation had violated federal air pollution rules at its plant in Kalamazoo, Michigan.
In 2008 Pfizer agreed to pay a $975,000 civil penalty to resolved federal charges that it violated the Clean Air Act at its former manufacturing plant in Groton, Connecticut in the period from 2002 to 2005.
Environmental groups in New Jersey have criticized as inadequate a clean-up plan devised by Pfizer and the EPA for the American Cyanamid Superfund site in Bridgewater, which is considered one of the worst toxic waste sites in the country. Pfizer inherited responsibility for the clean-up through its 2009 purchase of Wyeth.
______________________________________________________________________________________________________________________________________________________________
Dr Gary G. Kohls lives in the USA and writes articles that deal with the dangers of fascism, corporatism, totalitarianism, militarism, racism, malnutrition, and Big Pharma’s over-drugging and over-vaccinating agendas. In addition, his columns deal with cultural movements that threaten democracy, war, civility, health, freedom, the future of the children and the sustainability and livability of the planet.
January 21, 2022
Posted by aletho |
Corruption, Deception, Environmentalism, Science and Pseudo-Science, Timeless or most popular | Pfizer |
Leave a comment
Data should be fully and immediately available for public scrutiny
In the pages of The BMJ a decade ago, in the middle of a different pandemic, it came to light that governments around the world had spent billions stockpiling antivirals for influenza that had not been shown to reduce the risk of complications, hospital admissions, or death. The majority of trials that underpinned regulatory approval and government stockpiling of oseltamivir (Tamiflu) were sponsored by the manufacturer; most were unpublished, those that were published were ghostwritten by writers paid by the manufacturer, the people listed as principal authors lacked access to the raw data, and academics who requested access to the data for independent analysis were denied.1234
The Tamiflu saga heralded a decade of unprecedented attention to the importance of sharing clinical trial data.56 Public battles for drug company data,78 transparency campaigns with thousands of signatures,910 strengthened journal data sharing requirements,1112 explicit commitments from companies to share data,13 new data access website portals,8 and landmark transparency policies from medicines regulators1415 all promised a new era in data transparency.
Progress was made, but clearly not enough. The errors of the last pandemic are being repeated. Memories are short. Today, despite the global rollout of covid-19 vaccines and treatments, the anonymised participant level data underlying the trials for these new products remain inaccessible to doctors, researchers, and the public—and are likely to remain that way for years to come.16 This is morally indefensible for all trials, but especially for those involving major public health interventions.
Unacceptable delay
Pfizer’s pivotal covid vaccine trial was funded by the company and designed, run, analysed, and authored by Pfizer employees. The company and the contract research organisations that carried out the trial hold all the data.17 And Pfizer has indicated that it will not begin entertaining requests for trial data until May 2025, 24 months after the primary study completion date, which is listed on ClinicalTrials.gov as 15 May 2023 (NCT04368728).
The lack of access to data is consistent across vaccine manufacturers.16 Moderna says data “may be available … with publication of the final study results in 2022.”18 Datasets will be available “upon request and subject to review once the trial is complete,” which has an estimated primary completion date of 27 October 2022 (NCT04470427).
As of 31 December 2021, AstraZeneca may be ready to entertain requests for data from several of its large phase III trials.19 But actually obtaining data could be slow going. As its website explains, “timelines vary per request and can take up to a year upon full submission of the request.”20
Underlying data for covid-19 therapeutics are similarly hard to find. Published reports of Regeneron’s phase III trial of its monoclonal antibody therapy REGEN-COV flatly state that participant level data will not be made available to others.21 Should the drug be approved (and not just emergency authorised), sharing “will be considered.” For remdesivir, the US National Institutes of Health, which funded the trial, created a new portal to share data (https://accessclinicaldata.niaid.nih.gov/), but the dataset on offer is limited. An accompanying document explains: “The longitudinal data set only contains a small subset of the protocol and statistical analysis plan objectives.”
We are left with publications but no access to the underlying data on reasonable request. This is worrying for trial participants, researchers, clinicians, journal editors, policy makers, and the public. The journals that have published these primary studies may argue that they faced an awkward dilemma, caught between making the summary findings available quickly and upholding the best ethical values that support timely access to underlying data. In our view, there is no dilemma; the anonymised individual participant data from clinical trials must be made available for independent scrutiny.
Journal editors, systematic reviewers, and the writers of clinical practice guideline generally obtain little beyond a journal publication, but regulatory agencies receive far more granular data as part of the regulatory review process. In the words of the European Medicine Agency’s former executive director and senior medical officer, “relying solely on the publications of clinical trials in scientific journals as the basis of healthcare decisions is not a good idea … Drug regulators have been aware of this limitation for a long time and routinely obtain and assess the full documentation (rather than just publications).”22
Among regulators, the US Food and Drug Administration is believed to receive the most raw data but does not proactively release them. After a freedom of information request to the agency for Pfizer’s vaccine data, the FDA offered to release 500 pages a month, a process that would take decades to complete, arguing in court that publicly releasing data was slow owing to the need to first redact sensitive information.23 This month, however, a judge rejected the FDA’s offer and ordered the data be released at a rate of 55 000 pages a month. The data are to be made available on the requesting organisation’s website (phmpt.org).
In releasing thousands of pages of clinical trial documents, Health Canada and the EMA have also provided a degree of transparency that deserves acknowledgment.2425 Until recently, however, the data remained of limited utility, with copious redactions aimed at protecting trial blinding. But study reports with fewer redactions have been available since September 2021,2425 and missing appendices may be accessible through freedom of information requests.
Even so, anyone looking for participant level datasets may be disappointed because Health Canada and the EMA do not receive or analyse these data, and it remains to be seen how the FDA responds to the court order. Moreover, the FDA is producing data only for Pfizer’s vaccine; other manufacturers’ data cannot be requested until the vaccines are approved, which the Moderna and Johnson & Johnson vaccines are not. Industry, which holds the raw data, is not legally required to honour requests for access from independent researchers.
Like the FDA, and unlike its Canadian and European counterparts, the UK’s regulator—the Medicines and Healthcare Products Regulatory Agency—does not proactively release clinical trial documents, and it has also stopped posting information released in response to freedom of information requests on its website.26
Transparency and trust
As well as access to the underlying data, transparent decision making is essential. Regulators and public health bodies could release details27 such as why vaccine trials were not designed to test efficacy against infection and spread of SARS-CoV-2.28 Had regulators insisted on this outcome, countries would have learnt sooner about the effect of vaccines on transmission and been able to plan accordingly.29
Big pharma is the least trusted industry.30 At least three of the many companies making covid-19 vaccines have past criminal and civil settlements costing them billions of dollars.31 One pleaded guilty to fraud.31 Other companies have no pre-covid track record. Now the covid pandemic has minted many new pharma billionaires, and vaccine manufacturers have reported tens of billions in revenue.32
The BMJ supports vaccination policies based on sound evidence. As the global vaccine rollout continues, it cannot be justifiable or in the best interests of patients and the public that we are left to just trust “in the system,” with the distant hope that the underlying data may become available for independent scrutiny at some point in the future. The same applies to treatments for covid-19. Transparency is the key to building trust and an important route to answering people’s legitimate questions about the efficacy and safety of vaccines and treatments and the clinical and public health policies established for their use.
Twelve years ago we called for the immediate release of raw data from clinical trials.1 We reiterate that call now. Data must be available when trial results are announced, published, or used to justify regulatory decisions. There is no place for wholesale exemptions from good practice during a pandemic. The public has paid for covid-19 vaccines through vast public funding of research, and it is the public that takes on the balance of benefits and harms that accompany vaccination. The public, therefore, has a right and entitlement to those data, as well as to the interrogation of those data by experts.
Pharmaceutical companies are reaping vast profits without adequate independent scrutiny of their scientific claims.33 The purpose of regulators is not to dance to the tune of rich global corporations and enrich them further; it is to protect the health of their populations. We need complete data transparency for all studies, we need it in the public interest, and we need it now.
Footnotes
-
Competing interests: We have read and understood BMJ policy on declaration of interests and declare that The BMJ is a co-founder of the AllTrials campaign. PD was one of the Cochrane reviewers studying influenza antivirals beginning in 2009, who campaigned for access to data. He also helped organise the Coalition Advocating for Adequately Licensed Medicines (CAALM), which formally petitioned the FDA to refrain from fully approving any covid-19 vaccine this year (docket FDA-2021-P-0786). PD is also a member of Public Health and Medical Professionals for Transparency, which has sued the FDA to obtain the Pfizer covid-19 vaccine data. The views and opinions do not necessarily reflect the official policy or position of the University of Maryland.
-
Provenance and peer review: Commissioned; externally peer reviewed.
View Abstract
Author affiliations
Correspondence to: P Doshi Pdoshi@bmj.com
January 20, 2022
Posted by aletho |
Deception, Science and Pseudo-Science, Timeless or most popular | Covid-19, COVID-19 Vaccine, Human rights |
Leave a comment
The Chinese regime is doubling down in its “zero covid” strategy. In recent weeks, new covid cases have been detected in several cities. In a world of the more-contagious omicron variant, this is to be expected.
But what has been the Chinese state’s response? It’s more of the same. Lockdowns, travel suspensions, and more. NBC reports:
Tianjin, which detected China’s first community spread of Omicron on Saturday, is rolling out a second round of mass testing on its 14 million residents on Wednesday. …The outbreak has already spread to Anyang, a city in Henan province some 300 miles (482 kilometers) away, prompting a full lockdown …Tianjin officials said at a news conference Tuesday that all bus services to Beijing had been suspended. … On Wednesday, 425 flights were canceled at Tianjin Binhai International Airport, accounting for 95% of all scheduled flights… Tianjin authorities on Sunday ordered citizens not to leave the city unless absolutely necessary. Those who want to leave must present a negative Covid test taken within 48 hours…
It’s hard to believe that anyone still believes that covid will go away if government authorities just “lock down harder.” But China is hardly the only example of how this delusion can win many adherents among the technocrats and the expert class.
After all, let it not be forgotten that much of the world had adopted a zero covid policy early on, and this absurd policy endured for months. In Europe, of course, millions upon millions of people were virtually locked in their homes for months on end. As Philipp Bagus reported from Spain in spring of 2020, one wasn’t allowed to go outside without facing the wrath of state enforcers.
In America, the “experts” frequently spoke out in favor of zero covid, stating that lockdowns could eradicate the disease and that people would have to stay on lockdown until that time. For example, on April 2 of 2020, Anthony Fauci endorsed this idea, stating that social distancing requirements could not be relaxed until there are “essentially no new cases, no deaths for a period of time.” Hawaii explicitly embraced zero covid, and adopted a policy in 2020 based on the idea that public schools would never reopen until there was no longer any “community spread” and “no new cases” were detected over a period of four weeks.
Needless to say, those were totally unrealistic goals. They reflected only the plans of technocrats who were more concerned with living out their bizarre fetishes for lockdowns and border closures than with gaining a better grasp of the situation or with respecting basic human rights. Even Australia—an island nation that could perhaps plausibly hope to actually close its borders—has given up on the idea.
In other words, the “experts” in America wanted to recreate Chinese despotism in America. They adopted a lockdown policy that had already long been rejected. Lockdowns were already expected to bring long term side effects, such as surges in mental health problems—some of the worst of it among the young—now being reported by hospitals. The WHO even concluded that lockdowns ought to be rejected because “there is no obvious rationale for this measure.”
But perhaps the media and government officials were so successful at sowing panic in the general population in the spring of 2020 that the health technocrats saw their chance to try a new experiment in social engineering that they had previously considered unfeasible.
Fortunately, though, by the middle of 2020, it became clear that lockdowns simply weren’t going to be tolerated by much of the general public. Most state and local governments in the US abandoned zero covid rapidly, although the usual totalitarians in the media bemoaned the end of the policy, insisting that the abandonment of lockdowns would drench the non-lockdown jurisdictions in blood. This was predicted for US states like Georgia, and for countries like Sweden—where lockdowns were quickly jettisoned or not imposed at all.
As time went on, it became obvious that the non-lockdown jurisdictions did not fare significantly worse than the locked down ones. Some areas—Sweden, for instance—fared better. Some of the world’s harshest lockdown regimes—such as those in Peru, Argentina, the UK, and New York—also had some of the worst rates of deaths per million.
For the zero-covid crowd, reality got in the way.
Neo-Zero Covid: The Pivot to Vaccines
The zero covid mentality endures, however. The second wave of the zero covid mentality came with the idea that with universal vaccination, covid would disappear.
And, of course, once vaccines began to appear, it was hailed as a magic bullet that would ensure that the vaccinated would be unable to spread the disease. This ideology was expressed in a rant by Rachel Maddow who back in March 2020 harangued her viewers with the “fact” that “virus stops with every vaccinated person.” She continued: “A vaccinated person gets exposed to the virus, the virus does not infect them, the virus cannot then use that person to go anywhere else.”
This was all a complete fabrication. The vaccine never stopped the spread, and with the advent of the omicron variant, it’s now apparently the case that the vaccine doesn’t even slow the spread. The virus is quickly spreading among vaccinated.
It’s no longer possible to even pretend that vaccination prevents transmission. The only argument left to supporters of the vaccine mandate is that vaccines help against serious disease and death. That’s excellent, but it has nothing to do with public health because it’s clear the unvaccinated aren’t the reason the disease has not been eradicated.
And then there is the fact that vaccination has, in part, likely contributed to new covid mutations. This isn’t new with covid. The idea that treatments can lead to new mutations is not new, of course, and it’s long been known that under a variety of situations, leaky vaccines can produce vaccine resistant mutations.
This is also known to occur in the case of covid. For example, in an article for the Journal of Physical Chemistry (December 2021), the authors note “vaccine-breakthrough or antibody-resistant mutations provide a new mechanism of viral evolution.” And specifically on covid, they write how mutations are often more common in places with higher vaccination rates:
we reveal that the occurrence and frequency of vaccine-resistant mutations correlate strongly with the vaccination rates in Europe and America. We anticipate that as a complementary transmission pathway, vaccine-breakthrough or antibody-resistant mutations, like those in Omicron, will become a dominating mechanism of SARS-CoV-2 evolution when most of the world’s population is either vaccinated or infected.
This can make things even worse when coupled with other covid mitigation measures. As Vivek Ramaswamy and Apoorva Ramaswamy explained in the Wall Street Journal last week it’s simply not realistic to think vaccines can be constantly adjusted to keep up with new variants. And,
Meanwhile, mask mandates and social-distancing measures will have created fertile ground for new variants that evade vaccination even more effectively. Significant antigenic shifts may create new strains that are increasingly difficult to target with vaccines at all. There are no vaccines for many viruses, despite decades of effort to develop them.
That is, vaccination isn’t making covid go away. The politically correct version of the narrative also completely denies that the failure of vaccines to prevent the spread is even a significant factor in the spread of new mutations. The purveyors of the narrative still insist that only the unvaccinated have any responsibility in the continued existence of the disease. Consider, for example, a recent mainstream media report quoting a doctor who dutifully repeated the political orthodoxy that “Without a large percentage of people being vaccinated, the virus has been allowed to mutate.” Specifically, he further claimed that if “roughly 70% of the population” were vaccinated or naturally infected, this would bring the spread of the disease to a halt through “herd immunity.” But—as the doctor now intones in a forlorn voice—that can’t be achieved because there hasn’t been enough vaccination.
But given his criteria, we should expect places with at least 70% vaccination rates to have halted the spread of disease, right? Not surprisingly, this has not happened. In Portugal, for instance, the fully vaccinated rate—is at 90 percent. In Chile, it’s at 87 percent. It’s 75 percent in France. So, surely the spread of covid has been stopped in all these places? The answer is no. New cases are raging in Portugal, Chile, and France, with all these countries hitting new highs in recent days.
Whether we’re talking about vaccine mandates or lockdowns, it’s clear the zero covid strategy has been an abject failure. They’re still trying it in some places like China where government propaganda is largely unquestioned and where people practice unquestioning obedience to the regime at a scale that makes the all-too-complacent West look downright rebellious by comparison.
Don’t expect the “experts” in any country to give up on their slogans any time soon. But it is clear that reality will eventually catch up with them. Whether or not any respect for human rights remains at the end of it all is another matter.
January 20, 2022
Posted by aletho |
Civil Liberties, Science and Pseudo-Science, Timeless or most popular | China, Human rights, United States |
Leave a comment
UKHSA Vaccine Efficacy Statistics: Week 3
The UK Health Security Agency has been condemned for literally months now to report incredibly inconvenient vaccine efficacy statistics. How they have struggled. They have composed disclaimer after disclaimer. They filled a whole blog post with special pleading. They have greyed out the inconvenient numbers.
In their latest report, published just this evening, they’ve tried something new and bold. They now only calculate case, hospitalisation and death rates for the unvaccinated and the triple vaccinated. The double vaccinated have been banished entirely from Table 12. This will make the evil negative efficacy go away, right?
Ha, no:
The numbers are unadjusted, it is true; much certainty surrounds the size of the unvaccinated population and therefore case rates within that group. What is more, these are cases, not true infection statistics. Nevertheless, res ipsa loquitur. It does not look great.
In fact, the UKHSA have given us a great gift, in that they finally provide separate case and severe outcome statistics for the triple-vaccinated and the double vaccinated, allowing us to compare rates across all three groups. They don’t do that themselves, of course, but no matter. We can use the raw numbers and rates from last week’s report to derive the total number of double and triple vaccinated, and the rates in this week’s report to derive the triple vaccinated population. A little subtraction then gives us a decent estimate of how many double but not triple vaccinated people there are in each age bracket.
Here is the graph the UKHSA don’t want you to see:
This is plainly a pandemic of the vaccinated.
The double vaccinated death rate is also a problem. You can tell this just from looking at the numbers in each category:
The crucial 70+ demographic is over 90% boostered, and yet the very few double vaccinated in this cohort manage to match or exceed theeir death numbers.
The death rates have the double vaccinated worse than the unvaccinated in the 70+ cohort, and roughly matching the unvaccinated in the 60–69 group:
This isn’t all that surprising, given that Public Health Scotland data has shown across-the-board negative efficacy for the unboostered for some weeks now:
This is also true of deaths, but beware of the extremely low numbers, particularly in the singly vaccinated:
January 20, 2022
Posted by aletho |
Science and Pseudo-Science | Covid-19, COVID-19 Vaccine, UK |
Leave a comment
In 2019 Netflix in conjunction with WWF broadcast Frozen Worlds, an episode in the Our Planet series and narrated by David Attenborough. The scenes it showed shocked and horrified viewers around the world.
After a brief introduction about the recent loss of Arctic summer sea ice and the ‘inevitable’ devastation this will cause for Arctic animals, it shifts to a series of amazing shots of tens of thousands of walrus, crowded cheek-by-jowl on a beach in Siberia.
The camera pans out to a rocky cliff, which several walrus are attempting to climb. Then suddenly, one after another, the walrus are shown falling off the cliff to their deaths on the rocky shore below.The scenes are shown in slow motion and repeated in order to maximise the shock effect.
As the scenes unfold, Attenborough coolly informs viewers that the walrus would not normally be there, but out on the sea ice instead. But because of man-made global warming, the poor walrus have been forced onto land in crowded conditions, where they will inevitably suffer and die.
But was it all as simple as Attenborough portrayed?
A number of suspicions were immediately evident. Far from these beach haulouts being unusual, walrus in fact regularly use these beaches every year, in order to rest and feed while waiting for the sea ice to move south in autumn.
Walrus also invariably crowd together in these situations, both for warmth and protection from polar bears. Indeed, far from walrus being threatened by climate change, their populations have been growing in recent years, explaining why so many were hauled out that day.
And what made those walrus try to climb the cliff?
Dr Susan Crockford is a professional zoologist, who has specialised in Arctic mammals for many years, particularly polar bears and walrus. She immediately smelled a rat.
Her newly released book, Fallen Icon, tells the story of how she uncovered exactly what went on that day on the Siberian beach. Her detective work reveals how it was polar bears stalking them that forced the walrus up that cliff; how this is a common hunting tactic and how the bears then fed off the carcasses down below.
She uncovers evidence that WWF already knew about this hunting tactic at that particular location, and that was precisely why this beach was chosen for the film.
She goes on to describe how retreating sea ice actually increases the food supply for walrus and how their populations are both healthy and increasing.
And how Attenborough used this horrifying imagery to jump-start a three year campaign against human-caused global warming that included ten documentaries laden with groundless climate emergency messaging, much of it aimed at the wealthiest and most powerful people in the world. Attenborough’s relentless climate activism included a utopian vision of global changes for society eerily similar to the one proposed by the World Economic Forum.
It is hard to disagree with Crockford’s conclusions:
The public’s trust in science and medicine now appears to be at an all-time low. People who had been blind to the abuse of science rampant in the climate change narrative have had their eyes opened by the pandemic response. These things cannot be unseen.
In a worrying trend, traditional scientists struggle to be heard or have their concerns and criticisms published, both for climate change and Covid-19 related issues. Research that features testable hypotheses and reproducible studies seem to be rare birds while predictive modelling projects gobble up grant funds as well as the media attention.
Is science as we used to know it already dead? If so, how much of a role has Attenborough played in this progression? Over the last three years, he has used weaponized science presented to a trusting public in a most egregious manner.
My ultimate goal in writing this book is not to denigrate Sir David but to correct the misinformation he has deliberately or unwittingly promoted in his documentaries and public statements.
I am a traditional scientist standing up for science as it is meant to be – without activism and without politicization – because its loss to society will be incalculable.
Over the years but especially since 2018, Attenborough has shown that he lets others do his serious thinking for him and has often placed his trust where it was ill-advised, as he has done with the WWF. By that I mean he has relied on others to present information to him in an easily digestible manner rather than delving into the literature himself.
And having spent a lifetime taking this easy way out, when he decided he wanted his legacy to be something more substantial than ‘a good storyteller’, he seemed to take on the role of spokesman for others with ideological political agendas.
It appears to me that when he agreed to present the gruesome falling walrus film footage in Our Planet as evidence of climate change, Attenborough compromised his principles to achieve a specific end result. Such noble cause corruption is common in the conservation world but it was new for Attenborough.
I am convinced that what Attenborough has done with the falling walrus episode will be remembered long after he’s dead but not for the reasons he intended. It will go down as another ‘own goal’ for the climate change movement and judged as the moment Attenborough fell from grace as a trusted British icon.
Susan Crockford’s book is now available on Amazon here:
https://www.amazon.co.uk/dp/0991796691
Susan Crockford adds:
As I point out in my new book, Fallen Icon, David Attenborough devised a three year campaign on the falsehood that hundreds of Russian walrus died falling off a cliff due to climate change because he also desired what the World Economic Forum (WEF), meeting online this week, say they want: immediate and drastic changes, supposedly to mitigate an invisible ‘climate emergency’ and other societal ills.
Despite the fact that walrus and polar bears are thriving in the Arctic, this fabricated ’emergency’ seems to be the reason that its new chairman plans to make the G7 into a ‘climate club’.
January 20, 2022
Posted by aletho |
Book Review, Deception, Fake News, Mainstream Media, Warmongering, Science and Pseudo-Science, Timeless or most popular | Netflix, WWF |
Leave a comment
LAST October TCW reported on the concerning numbers of miscarriages and stillbirths reported to our drugs watchdog, the Medicines and Healthcare products Regulatory Agency (MHRA).
Pregnant women who had received a Covid jab and then lost their baby filled out Yellow Card reports in their hundreds. At that time nearly 600 mothers-to-be had suffered spontaneous abortions, as the MHRA refer to miscarriages, and felt the jab had been responsible. In just three months, that number increased by 100 to a total of 709.
Pfizer’s jab is associated with the highest casualty rate, with 425 miscarriages reported. That figure includes one premature baby death, one miscarriage-related death and 13 stillbirth/foetal deaths. Since May last year, the under-40s have not received the Oxford/AstraZeneca vaccine because it increases your risk of developing blood clots. AZ, introduced in January 2021, still has 229 reports of miscarriage with five stillbirths, while the Moderna jab, introduced in April 2021, has 51 miscarriage reports. Five mothers reported they did not know which vaccine they had received.
Since February last year, the BBC have been urging pregnant women to take the Covid vaccination despite the fact that no manufacturer was due to complete a scientific trial in expectant mothers before December. Their results are still to be released so all we have is the MHRA’s real-time data, which it seems is being ignored.
Instead, British health chiefs have relied on information from women in the US who accidentally found themselves pregnant having taken the Covid jab and reported the results of their pregnancy to the V-safe app. V-safe is hosted by the US Centers for Disease Control (CDC) but it is not a scientific study. It is a self-reporting database like the MHRA Yellow Card scheme which Reuters fact checkers like to tell us should not be relied on. So if we cannot rely on the Yellow Card, how can we rely on V-safe?
‘We cannot,’ said an obstetrician who did not want to be named, based in Scotland. ‘Frankly, it’s a mess and when you consider what is at stake, the healthy development of a baby, and the health of the mother, it’s a disgrace.’
This fact has not been acknowledged by the Royal College of Obstetricians and Gynaecologists, who updated their advice to pregnant and nursing mothers on 20 December 2021. They said: ‘Covid-19 vaccines are strongly recommended in pregnancy. Vaccination is the best way to protect against the known risks of Covid-19 in pregnancy for both women and babies, including admission of the woman to intensive care and premature birth of the baby.’
Three months ago TCW exposed how figures had been manipulated by the NHS to make unvaccinated pregnant mums think they had a higher risk of ending up in ICU than vaccinated mums. It was not true.
The chief scientific adviser to the Department of Health, Professor Lucy Chappell, has never satisfactorily addressed parents’ concerns about whether the vaccine can harm their unborn babies. Ms Chappell, who is also Professor in Obstetrics at King’s College London, tweeted last November: ‘Covid-19 vaccines have protected millions of women around the world – and are safe for pregnant women and women considering pregnancy.’ The tweet had a cool reception with just 116 likes and Dr Chappell had no data from any vaccine manufacturer to support her claim.
The same applies to MHRA chief executive Dr June Raine, who said in a statement in November: ‘We want to reassure all pregnant women that the Covid-19 vaccines are safe and effective for them to use at all stages of pregnancy. Our rigorous safety monitoring of these vaccines in pregnancy shows that the vaccines are safe and that there is no increased risk of pregnancy complications, miscarriage, or stillbirth.’
A British funeral director known only as Wesley tells another story. On camera, he says how he saw newborn baby deaths increase tenfold after vaccination began.
Wesley says: ‘There are a lot of newborn babies in fridges in mortuaries. There were 30 in one hospital. Mortuary fridges usually hold about 6-10 babies maximum and they’re never normally full. ‘Now, they’re full and (the deceased babies) are being kept in the adult section.’ He agreed with the interviewer that the number was ten times higher than normal, and went on: ‘The babies have either been miscarried or they are full term stillbirths but not a lot has been said about it.’
If anyone wants to speak out, we promise we are listening.
Latest Yellow Card scheme figures published below with 1,932 fatalities reported to January 5 2022.
Adult – Primary & Booster/Third Dose, Child Administration
Pfizer – 25.3million people – 47.2m doses – Yellow Card reporting rate – 1 in 162 people impacted
AstraZeneca – 24.9m people – 49.1m doses – Yellow Card reporting rate – 1 in 103 people impacted
Moderna – 1.6m people – 3m doses – Yellow Card reporting rate – 1 in 50 people impacted
Overall, 1 in 120 people injected experiences a Yellow Card adverse event. A significant proportion require urgent medical care, may be life changing or long-lasting in effect. This may be less than 10 per cent of actual figures according to MHRA.
Adult Booster or 3rd Doses = 34,834,288 people
Booster Yellow Card Reports – 24,402 (Pfizer) + 371 (AZ) + 13,156 (Moderna) + 121 (Unknown) = 38,050
Reactions – 446,903 (Pfizer) + 855,968 (AZ) + 106,996 (Moderna) + 4,426 (Unknown) = 1,414,293
Reports – 156,250 (Pfizer) + 241,657 (AZ) + 32,133 (Moderna) + 1,442 (Unknown) = 431,482 people impacted
Fatal – 684 (Pfizer) + 1182 (AZ) + 29 (Moderna) + 37 (Unknown) = 1,932
Spontaneous Abortions – 425 + 1 premature baby death + 1 miscarriage related death/ 13 stillbirth/foetal deaths (9 recorded as fatal) (Pfizer) + 229 + 5 stillbirth (AZ) + 51 (Moderna) + 4 (Unknown) = 709 miscarriages
Blood Disorders – 16,056 (Pfizer) + 7,728 (AZ) + 2,228 (Moderna) + 62 (Unknown) = 26,074
Pulmonary Embolism & Deep Vein Thrombosis – 801 (Pfizer) + 2,991 (AZ) + 73 (Moderna) + 25 (Unknown) = 3,890
Anaphylaxis – 615 (Pfizer) + 863 (AZ) + 76 (Moderna) + 2 (Unknown) = 1,556
Acute Cardiac – 10,703 (Pfizer) + 10,766 (AZ) + 2,408 (Moderna) + 83 (Unknown) = 23,960
Pericarditis/Myocarditis – 1,047 (Pfizer) + 414 (AZ) + 256 (Moderna) + 6 (Unknown) = 1,723
Infections – 10,568 (Pfizer) + 19,679 (AZ) + 1,861 (Moderna) + 136 (Unknown) = 32,244
Herpes – 2,048 (Pfizer) + 2,639 (AZ) + 208 (Moderna) + 20 (Unknown) = 4915
Blindness – 142 (Pfizer) + 309 (AZ) + 23 (Moderna) + 4 (Unknown) = 478
Eye Disorders – 7,310 (Pfizer) + 14,641 (AZ) + 1,276 (Moderna) + 82 (Unknown) = 23,309
Deafness – 268 (Pfizer) + 418 (AZ) + 40 (Moderna) + 4 (Unknown) = 730
Skin Disorders – 31,329 (Pfizer) + 52,749 (AZ) + 11,702 (Moderna) + 308 (Unknown) = 96,088
Psychiatric Disorders – 9,307 (Pfizer) + 18,117 (AZ) + 2,075 (Moderna) + 104 (Unknown) = 29,603
Headaches & Migraines – 33,635 (Pfizer) + 93,545 (AZ) + 8,280 (Moderna) + 323 (Unknown) = 135,783
Vomiting – 4,914 (Pfizer) + 11,594 (AZ) + 1,587 (Moderna) + 59 (Unknown) = 18,154
Nervous System Disorders – 75,192 (Pfizer) + 180,996 (AZ) + 17,398 (Moderna) + 816 (Unknown) = 274,402
Strokes and CNS haemorrhages – 707 (Pfizer) + 2,245 (AZ) + 34 (Moderna) + 13 (Unknown) = 2,999
Guillain-Barré Syndrome – 83 (Pfizer) + 483 (AZ) + 9 (Moderna) + 6 (Unknown) = 581
Facial Paralysis including Bell’s Palsy – 1,001 (Pfizer) + 978 (AZ) + 119 (Moderna) + 10 (Unknown) = 2,108
Tremor – 2,020 (Pfizer) + 9,897 (AZ) + 570 (Moderna) + 50 (Unknown) = 13,538
Seizures – 1,023 (Pfizer) + 2,028 (AZ) + 232 (Moderna) + 16 (Unknown) = 3,299
Paralysis – 463 (Pfizer) + 855 (AZ) + 81 (Moderna) + 8 (Unknown) = 1,407
Respiratory Disorders – 19,633 (Pfizer) + 29,211 (AZ) + 3,489 (Moderna) + 185 (Unknown) = 52,518
Reproductive/Breast Disorders – 27,738 (Pfizer) + 20,196 (AZ) + 4,211 (Moderna) + 177 (Unknown) = 52,322
CHILDREN & YOUNG PEOPLE SPECIAL REPORT
Suspected side effects reported in individuals under 18
Pfizer – 3,000,000 children (1st doses) plus 900,000 second doses resulting in 2,471 Yellow Cards
AZ – 11,600 children (1st doses) plus 10,000 second doses resulting in 248 Yellow Cards – Reporting rate 1 in 47
Moderna – 21,500 children (1st doses) and 16,000 second doses resulting in 16 Yellow cards
Brand Unspecified – 11 Yellow Cards
Total = 3,033,100 children injected
Total Yellow Cards Under 18s = 2,746
Full reports including 339 pages of specific reaction listings are here.
January 19, 2022
Posted by aletho |
Deception, Science and Pseudo-Science, Timeless or most popular, War Crimes | Covid-19, COVID-19 Vaccine, Royal College of Obstetricians and Gynaecologists, UK |
Leave a comment

Joe Biden introduced his “new” plan to save us from the dread coronavirus. He will provide 500 million “free” tests (paid for by taxpayers or with borrowed money); 1,000 National Guard troops to overstressed hospitals; and more pressure to get vaccinated and boosted.
According to the Kaiser Family Foundation, we would need 2.3 billion tests per month to test every person over age 12 twice per week at the recommended frequency of twice per week. What type of test, and where would we get them? Pharmacies are running out of home antigen tests. We have no data on the likelihood of false negative or false positive tests, but we do know that with any test, even very good ones, the vast majority of positive tests will be false positives if only a small percentage of the tested group is diseased. Also, tests may remain positive long after a person has recovered and is no longer infectious.
Can the tests harm? False positives lead to isolation with destruction of livelihoods and educational opportunities. We may be having an epidemic of false positive PCR tests. Using too high a cycle threshold, as some labs have routinely done, gives a meaningless result. And from your lab report, you cannot tell what cycle threshold was used.
It is possible that doing the test itself could be fatal. A few military members reportedly had infections with flesh-eating bacteria after getting swabbed, and some of the swabs were found to be contaminated. At least one patient got meningitis when a nasal swab was inserted too far.
Hospitals are indeed overstressed. According to a talk radio host, patients are dying in the halls and waiting room of a local hospital because of short staffing. Will 1,000 troops help? Mayo alone just fired 700 unvaccinated workers. An Ohio physician reported that the troops were causing chaos. They didn’t even know where supplies were kept, and after a 12-hour shift might be dispatched to another state before they had time to learn the local system. Under CMS waivers covering the declared emergency, minimally qualified personnel may be used. And now the most experienced and dedicated workers, the very ones most likely to exercise independent judgment and stand up for patients, are being culled.
Will more vaccines and boosters help? Biden asserts that it’s a “patriotic duty” to get jabbed, and more jabs are the only way to end the disaster. No matter how much respect you have for his mental abilities, he is likely quoting the American Medical Association. The jabs do not appear to be effective against the new variants, and might even be creating them. There is talk of a fourth shot—but apparently no stopping point for adverse effects such as myocarditis in children.
The U.S. has one of the worst records in the world for controlling COVID-19. Moreover, the most reliable source of statistics, insurance actuaries, shows that deaths in the prime working age group are up 40 percent, and disability claims are also up. A 10 percent increase would be the equivalent of a 200-year flood. The claims are not citing COVID-19 as a cause of death. They could be collateral damage from government policy, including poor medical care for virtually everything, or they could be from vaccination.
States are pushing back against the mandates, which are being imposed by executive order through unaccountable administrative agencies. The U.S. Supreme Court should be considering whether the administrative state has the constitutional or statutory authority to impose a medical dictatorship that overrides the states’ authority and citizens’ basic rights. Some Justices, however, seem to be taking the-end-justifies-the-means approach—and that based on egregiously erroneous information. For example, Justice Breyer asserted that there were 750 million cases (in a population of about 330 million) and Justice Sotomayor asserted that there were 100,000 hospitalized children (instead of fewer than 4,000, mostly not for COVID-19). The harms from the mandated vaccines were simply ignored.
Even if the “experts” Biden is relying upon, under the titular leadership of Anthony Fauci, were right this time, the precedent could grant unlimited power to a medical dictatorship to force disastrous policy on all Americans.
Instead of endlessly repeating failed policy, how about firing the generals who are in charge of the losing war?
January 19, 2022
Posted by aletho |
Science and Pseudo-Science | Covid-19, COVID-19 Vaccine, Joe Biden, United States |
Leave a comment
The Pfizer-sponsored CDC Foundation has teamed up with Big Tech and Big Pharma giants Facebook and Merck, among others, in order to promote Covid vaccines.
The pressure group calls itself the Alliance for Advancing Health Online and some details about its purpose and organization are revealed in an email sent to the White House and obtained and shared by the Informed Consent Action Network (ICAN).

Other than the CDC Foundation, Facebook’s partners are the World Health Organization, the World Bank, the MIT Initiative on the Digital Economy, Sabin Vaccine Institute, the Bay Area Global Health Alliance, and the Vaccine Confidence Project at the London School of Hygiene and Tropical Medicine.
During the fiscal years 2014 through 2018, the CDC Foundation reportedly received $79.6 million from companies Pfizer, Biogen, Merck, and others. Pfizer continues to be listed as a current donor.
ICAN noted that it emerges from the email – sent by Facebook’s US Public Policy head Payton Iheme – that the purpose of the initiative is to use social media and platforms “to build confidence in and drive uptake of vaccines.”
ICAN is a network whose mission is to promote putting authority over health choices in the hands of people whom these decisions affect, and parse out true medical information from that tainted by financial interest and advertising, which, they say, leads to “medical coercion” rather than tangible understanding of issues.
Now the group is suggesting there is conflict in the CDC Foundation forming an alliance to drive home the message of the need to get vaccinated as a matter of public health concern – when those selling the vaccines are members of that alliance. This is particularly pertinent as Facebook has been censoring some criticism of Pfizer vaccines.
The Centers for Disease Control and Prevention (CDC) is the US public health agency, but it is a handy technicality in this and similar instances that the CDC Foundation has been set up as a private nonprofit incorporated in Georgia, established by Congress through the Public Health Service Act.
Facebook and Merck are throwing in $40 million each to start off the operation, and the money will go towards research into “advancing public understanding of how social media and behavioral sciences can be leveraged to improve the health of communities around the world.”
The first grants will be given to researchers and organizations who are exploring ways of using social media and digital platforms to build confidence in and drive uptake of vaccines, the email said.
Facebook’s representative also wrote that the corporation and its partners in the alliance are looking to expand their work.
January 19, 2022
Posted by aletho |
Corruption, Deception, Science and Pseudo-Science | COVID-19 Vaccine |
Leave a comment
… and more bad news for “the experts”
it’s becoming a bit like beating a dead horse to keep highlighting more and more data that shows the failure of the vaccines to act as promised, but this one highlights something else i was discussing recently and provides a tangible example of the math and definitional manipulation that’s going on.
so let’s take a quick spin:
(all data from HERE)
first, cases:
as is becoming endlessly apparent and replicable, “unvaxxed” is outperforming every other category.
vaccines are not stopping spread, they are most likely (subject to the limitations of non randomized society scale data) accelerating it.
this becomes readily apparent when we calculate risk ratios. (incidence of group divided by incidence in unvaxxed control, so any number >1 = more risk)
risk in the double vaxxed is well over twice as high as in the unvaxxed. boosters seem to help, but still cannot get you back to baseline and i want to emphasize the word “seem” here because i think this data is misleading and is vastly overstating booster efficacy and likely making double vaxxed look worse than it is. (more in a minute)
we can also look at hospitalization:
what’s most interesting here is that it seems like there was some vaccine efficacy against hospitalization but that it inverted as 2022 began.
we can see the risk ratio on 2 doses rise sharply from 0.76 (24% VE) to 1.39 (-39% VE). this is an 82% jump in risk ratio and it was durable into the following week. i have emphasized this in red.
boosters seem effective (but there’s that word again) but even this seeming efficacy is rapidly dropping and risk ratio is up from 0.15 in week 3 dec to 0.38 in week 2 jan, a 150% change.
i see 2 likely explanations here and they are not mutually exclusive:
- this is omicron, the OAS/vaccine (Original Antigenic Sin) evading variant showing up and taking over. as it does, vaccine efficacy drops like a rock because you are antigenically imprinted for the wrong spike proteins. what had been a help becomes actual harm because a bad response is worse for you than making one up on the fly and omicron is the optimized output of selection by leaky vaccine for vaccine evasion and superspread. we’re now into OAS territory, just as certain gatos told you we would be…
- this is bad math and bad definitions being used to hide properties of these vaccines and shift risk. defining as “3 doses” only those 2 weeks after their 3rd jab is bayesian datacrime, especially when the jab itself is known to cause ~2 weeks of immunosuppression and higher risk. the jab itself generates a high risk cohort but then attributes that risk to the cohort before it. it’s like blaming getting hit by a car crossing the street on having stayed on the sidewalk, and the effects can be gigantic. you can hide ANYTHING in that. it’s bad definitions leading to bad math and it’s been widespread practice since pfizer ginned it up to slant their trials.
you can get a full walk through on this issue and the various forms in which is can manifest here:
the bottom line is that this is literally a card shark palming a bad card out of his hand and dropping it into yours. lumping this 2 week risk period into the group that did not get the most recent round of vaxxes is an absurd risk shifter. it will always make whatever the new round of vaccines is look like it’s working.
the examples linked about lay it out clearly: you can make a zero efficacy vaxx look like it works and this works even better if it causes a rise in risk in the 2 week period you lump into the prior group.
thus, boosters make “full vaxxed” look bad. fully vaxxed made unvaxxed look bad. so much of what has been claimed to be vaccine efficacy is just a mathematic rig job from poorly chosen definitions and there is simply no way that that was an accident.
pfizer does not make mistakes like that or like vaxxing the whole control group right when vaxx fade started to get bad. they make choices and those choices have been aided and abetted by regulators and public health agencies.
they all signed off on and adopted these misleading definitions and have been providing information and making policy based upon them.
i’m willing to believe that the CDC was too inept to spot this. it’s sad, but it’s plausible.
but the NIH should have seen it and the FDA not only should have spotted it instantly but should have disallowed a trial using such a shady tactic. it’s pure manipulation.
they both let it go because they were both involved. NIH licensed the IP for the vaccine payload to moderna. former FDA head gottlieb stepped down mid-term to join the pfizer board of directors.
this is what full blown regulatory capture looks like… Full article
January 19, 2022
Posted by aletho |
Deception, Science and Pseudo-Science, Timeless or most popular | COVID-19 Vaccine |
Leave a comment
The momentum feels to me like it is accelerating…
Some narrative pieces have been falling apart were recently brought to my attention.
Here are the four new truths:
- The vaccines make you more likely to get COVID: It was supposed to make things better, but we’re basically mandating you get a shot that makes you more likely to get infected. That is totally insane, but that’s what we are doing. Check out the graphs here. No age confounding this time: UK Government Data proves the Covid-19 Vaccines DOUBLE your chances of catching Covid-19.
- The vaccines aren’t safe: I’m now hearing a lot from prominent formerly pro-vax docs that they are turning on the vaccine. This is great news. Nobody is going public yet, but they are all pissed and realize they have been misled. It will not be pretty. This is of course great news.
- Cloth masks don’t work: The CDC finally admits that cloth masks that they said worked before and that everyone wore (including Rochelle Walensky) don’t actually work. The other mask types don’t work either, but it will take them longer to figure out the obvious. P100 respirators do work but only a small percentage of people know that. I can’t wait to see Rochelle Walensky wear a P100 respirator; after all, she should be modelling best practices.
- Kids shouldn’t have boosters shots: Top WHO scientist finally admits that kids shouldn’t get boosted!!!! Yet the US colleges and universities aren’t going to back off. Someone is very wrong here and for once it isn’t the WHO.
Here are some older truths that should have been realized by now, but are still going on:
- Remdesivir is killing patients, not saving them: RDV is standard operating procedure in the US, but everyone I talk to says it doesn’t work and is much more likely to kill patients than save them. Doctors are forced to give it by hospital policy.
- Social distancing doesn’t work: The MIT study came out in April, 2021 that showed social distancing makes no difference. 6 feet or 60 feet made no difference. People still haven’t figured this out.
January 19, 2022
Posted by aletho |
Science and Pseudo-Science | Covid-19, COVID-19 Vaccine |
Leave a comment