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COVID-19

Health researcher calls government promotion of Covid mRNA vaccines “confusing”

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5 minute read

From (2079) Dr. John Campbell – YouTube

British Health researcher John Campbell has uncovered sobering and disturbing statistics regarding serious adverse events connected to covid vaccines.

As Campbell outlines in this presentation, multiple previous vaccines producing far fewer adverse events, have been withdrawn from public use while governments continue to promote covid vaccines.

(Campbell is well known for his meticulous research and he always includes links to the studies he is calling attention to.  His presentation notes are below the video) 

John Campbell’s research notes and links to relevant studies

Swine flu vaccine (1976), 1 serious event per 100,000 vaccinees,

Vaccine withdrawn Rotavirus vaccine

Rotashield, (1999),1 to 2 serious events per 10,000 vaccinees,

Vaccine withdrawn

Covid mRNA vaccines, 1 serious event per 800 vaccinees,

Vaccine officially promoted

Serious adverse events of special interest following mRNA COVID-19 vaccination in randomized trials in adults https://pubmed.ncbi.nlm.nih.gov/36055…

Free full text available https://www.ncbi.nlm.nih.gov/pmc/arti…

Why We Question the Safety Profile of mRNA COVID-19 Vaccines (Robert M Kaplan and Sander Greenland) https://sensiblemed.substack.com/p/wh…

Using publicly available data from Pfizer and Moderna studies, we found one serious adverse event for each 800 vaccinees. That translates to about 1,250 serious events for each million vaccine recipients.

US, Spain, Australia

Study to evaluate serious adverse events of special interest observed in mRNA COVID-19 vaccine trials.

Secondary analysis of serious adverse events reported in the placebo-controlled, phase III randomized clinical trials, of Pfizer and Moderna mRNA COVID-19 vaccines

Results Pfizer and Moderna mRNA COVID-19 vaccines were associated with an excess risk of serious adverse events

of special interest

Pfizer

10.1 per 10,000 vaccinated over placebo baselines of 17.6

Moderna

15.1 per 10,000 vaccinated over placebo baseline of 42.2

Combined, the mRNA vaccines Associated with an excess risk of serious adverse events of special interest of 12.5 per 10,000 vaccinated

Pfizer trial

Pfizer vaccine group 52 serious AESI (27.7 per 10,000) were reported

Pfizer placebo group 33 serious AESI (17.6 per 10,000) were reported

36 % higher risk of serious adverse events in the vaccine group

Risk difference 18.0 per 10,000 vaccinated

Moderna trial

Moderna trial, vaccine group 87 serious AESI (57.3 per 10,000) were reported

Moderna trial, placebo group 64 serious AESI (42.2 per 10,000) were reported

6 % higher risk of serious adverse events in the vaccine group

Risk difference 7.1 per 10,000 vaccinated

Discussion

The excess risk of serious adverse events found in our study points to the need for formal harm-benefit analyses, particularly those that are stratified according to risk of serious COVID-19 outcomes. These analyses will require public release of participant level datasets. Full transparency of the COVID-19 vaccine clinical trial data is needed, to properly evaluate these questions.

Unfortunately, as we approach 2 years after release of COVID-19 vaccines, participant level data remain inaccessible.

Level of adverse reactions in the past

The 1976 swine flu vaccine

Small increased risk of Guillain-Barré Syndrome

The increased risk was approximately 1 additional case of GBS for every 100,000 people who got the swine flu vaccine. When over 40 million people were vaccinated against swine flu, federal health officials decided that the possibility of an association of GBS with the vaccine, however small, necessitated stopping immunization until the issue could be explored.

The Institute of Medicine (2003) https://www.ncbi.nlm.nih.gov/books/NB…

Concluded that people who received the 1976 swine influenza vaccine had an increased risk for developing GBS. Exact reason for this association remains unknown.

Rotavirus vaccine Rotashield, (1999) https://www.cdc.gov/vaccines/vpd-vac/…

The U.S. Advisory Committee on Immunization Practices (ACIP) October 22, 1999 to no longer recommend use of the RotaShield® vaccine for infants, because of an association between the vaccine and intussusception. The results of the investigations showed that RotaShield® vaccine caused intussusception in some healthy infants Within 2 weeks Intussusception increased 20 to 30 times over the expected risk (Less after the second and third dose) CDC estimated that one or two additional cases of intussusception would be caused among each 10,000 infants vaccinated with RotaShield® vaccine.

 

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COVID-19

Pfizer reportedly withheld presence of cancer-linked DNA in COVID jabs from FDA, Health Canada

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From LifeSiteNews

By Clare Marie Merkowsky

According to information released by the Epoch Times, Pfizer purposefully failed to advise drug regulators, including Health Canada, the U.S. FDA and the European Medicines Agency, that the cancer-linked SV40 DNA enhancer was present in their experimental COVID shot.

Pharmaceutical giant Pfizer reportedly “chose not to” inform Health Canada, the U.S. Food and Drug Administration and other regulatory agencies that the cancer-linked Polyomavirus Simian Virus 40 (SV40) DNA sequence was in their widely distributed COVID-19 vaccine.  

According to information released April 23 by the Epoch Times, Pfizer purposefully failed to advise drug regulators, including Health Canada, the U.S. Food and Drugs Administration, and the European Medicines Agency, that SV40 was present in their experimental COVID shot.   

“I understand that there have been internal discussions at CBER [Center for Biologics Evaluation and Research] regarding the presents [sic] of an SV40 enhancer/promoter sequence, noting that its presence is unrelated to the purpose of the Pfizer’s plasmid as a transcription template for their mRNA COVID-19 vaccine,” Dr. Dean Smith, a senior scientific evaluator in Health Canada’s Vaccine Quality Division, wrote in an email to a colleague at the FDA about SV40. 

The August email was obtained by an access to information request by the Epoch Times.  

“Pfizer has communicated to us recently, that they apparently chose not to mention this information to EMA, FDA or HC at the time of their initial or subsequent submissions,” he added. 

Smith noted that Kevin McKernan, a microbiologist and former researcher and team leader for the MIT Human Genome project, and Dr. Phillip J. Buckhaults, who is a professor of cancer genomics as well as the director of the Cancer Genetics Lab at the University of South Carolina, had raised in a public manner earlier this year how SV40 was present in the jabs. 

While Health Canada originally told Canadians it was unaware of the SV40 enhancer’s presence, the agency has since confirmed the presence of the monkey-linked DNA sequence known to cause cancer when it was used in old polio vaccines. 

SV40 is used to enhance gene transcription when the shots are made. It has been linked to the spread of turbo cancers in those who have been exposed to the virus via contaminated injections.   

According to a 2002 study published in the Lancet, there is evidence that links the older polio vaccines, which were filed with SV40 contaminants, to certain forms of cancer.  

The authors of the 2002 study claim that the SV40-contaminated polio vaccine may have caused up to half of the 55,000 cases of non-Hodgkin’s lymphoma diagnosed each year.  

SV40, according to the late vaccine developer Dr. Maurice Hilleman, was put in the polio vaccine and then put into wide circulation by Big Pharma company Merck inadvertently. 

Unfortunately, this is not the first evidence that Pfizer hid the presence of SV40 from drug regulators.  

According to Dr. Janci Lindsay, who works as the director of toxicology and molecular biology for Toxicology Support Services, Pfizer did not disclose the presence of SV40 “promoters” to both Health Canada and the U.S. Food and Drug Administration, as well as the European Medicines Agency.  

She said, as reported in The Epoch Times, that the drug company “hid them.” 

“So it’s not just the fact that they’re there, it’s the fact that they were purposefully hidden from the regulators,” she noted. 

The news of Pfizer’s purposeful withholding of information comes as adverse effects from the first round of COVID shots have resulted in a growing number of Canadians who have filed for financial compensation over alleged injuries from the jabs, via Canada’s Vaccine Injury Program (VISP). 

Thus far, some VISP has already paid over $6 million to those injured by COVID injections, with some 2,000 claims remaining to be settled. 

Additionally, a recent study done by researchers with Canada-based Correlation Research in the Public Interest showed that 17 countries have found a “definite causal link” between peaks in all-cause mortality and the fast rollouts of the COVID shots as well as boosters. 

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Alberta

Red Deer Doctor critical of Alberta’s COVID response to submit report to Danielle Smith this May

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From LifeSiteNews

By Anthony Murdoch

Leading the task force is Dr. Gary Davidson, who was skeptical of mandates at the time.

Alberta Premier Danielle Smith will soon be receiving a little-known report she commissioned which tasked an Alberta doctor who was critical of the previous administration’s handling of COVID to look into how accurate the province’s COVID data collection was, as well as the previous administration’s decision-making process and effectiveness. 

As noted in a recent Globe and Mail report, records it obtained show that just less than one month after becoming Premier of Alberta in November of 2022, Smith tasked then-health minister Jason Copping to create the COVID data task force. 

Documents show that the Alberta government under Smith gave the new task force, led by Dr. Gary Davidson – who used to work as an emergency doctor in Red Deer, Alberta – a sweeping mandate to look at whether the “right data” was obtained during COVID as well as to assess the “integrity, validity, reliability and quality of the data/information used to inform pandemic decisions” by members of Alberta Health Services (AHS).  

As reported by LifeSiteNews in 2021, Davidson said during the height of COVID that the hospital capacity crisis in his province was “created,” was not a new phenomenon, and had nothing to do with COVID.

“We have a crisis, and we have a crisis because we have no staff, because our staff quit, because they’re burned out, they’re not burnt out from COVID,” Davidson said at the time. 

Davidson also claimed that the previous United Conservative Party government under former Premier Jason Kenney had been manipulating COVID statistics.  

In comments sent to the media, Smith said that in her view it was a good idea to have a “contrarian perspective” with Davidson looking at “everything that happened with some fresh eyes.” 

“I needed somebody who was going to look at everything that happened with some fresh eyes and maybe with a little bit of a contrarian perspective because we’ve only ever been given one perspective,” she told reporters Tuesday. 

“I left it to [Davidson] to assemble the panel with the guidance that I would like to have a broad range of perspectives.” 

After assuming her role as premier, Smith promptly fired the province’s top doctor, Deena Hinshaw, and the entire AHS board of directors, all of whom oversaw the implementation of COVID mandates. 

Under Kenney, thousands of nurses, doctors, and other healthcare and government workers lost their jobs for choosing to not get the jabs, leading Smith to say – only minutes after being sworn in – that over the past year the “unvaccinated” were the “most discriminated against” group of people in her lifetime. 

As for AHS, it still is promoting the COVID shots, for babies as young as six months old, as recently reported by LifeSiteNews.  

Task force made up of doctors both for and against COVID mandates  

In addition to COVID skeptic Dr. Gary Davidson, the rather secretive COVID task force includes other health professionals who were critical of COVID mandates and health restrictions, including vaccine mandates.  

The task force was given about $2 million to conduct its review, according to The Globe and Mail, and is completely separate from another task force headed by former Canadian MP Preston Manning, who led the Reform Party for years before it merged with another party to form the modern-day Conservative Party of Canada. 

Manning’s task force, known as the Public Health Emergencies Governance Review Panel (PHEGRP), released its findings last year. It recommend that many pro-freedom policies be implemented, such as strengthening personal medical freedoms via legislation so that one does not lose their job for refusing a vaccine, as well as concluding that Albertans’ rights were indeed infringed upon. 

The Smith government task force is run through the Health Quality Council of Alberta (HQCA) which is a provincial agency involved in healthcare research.  

Last March, Davidson was given a project description and terms of reference and was told to have a final report delivered to Alberta’s Health Minister by December of 2023. 

As of now, the task force’s final report won’t be available until May, as per Andrea Smith, press secretary to Health Minister Adriana LaGrange, who noted that the goal of the task force is to look at Alberta’s COVID response compared to other provinces.  

According to the Globe and Mail report, another person working on the task force is anesthetist Blaine Achen, who was part of a group of doctors that legally challenged AHS’s now-rescinded mandatory COVID jab policy for workers. 

Some doctors on the task force, whom the Globe and Mail noted held “more conventional views regarding the pandemic,” left it only after a few meetings. 

In a seeming attempt to prevent another draconian crackdown on civil liberties, the UCP government under Smith has already taken concrete action.

The Smith government late last year passed a new law, Bill 6, or the Public Health Amendment Act, that holds politicians accountable in times of a health crisis by putting sole decision-making on them for health matters instead of unelected medical officers. 

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