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COVID-19 Vaccines Neither Safe, Nor Effective #180180
09/20/2023 09:10 AM
09/20/2023 09:10 AM
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COVID-19 Vaccines Revealed To Be ‘Neither Safe, Nor Effective’: Watchdog

Authored by Naveen Athrappully via The Epoch Times (emphasis ours),

COVID-19 vaccines were authorized in Canada during 2020 and 2021 without being subjected to the country’s safety tests as required under established drug regulations, revealed an accountability watchdog.
A medical assistant holds a tray of syringes filled with doses of Moderna COVID-19 vaccine at a vaccination site in Los Angeles on Feb. 16, 2021. (Apu Gomes/AFP via Getty Images)

An investigation into COVID vaccines found that the jabs were “neither safe nor effective,” said the nonprofit National Citizens Inquiry (NCI) in a Sept. 15 post on X. The organization published a report Thursday detailing the flawed mechanism through which the vaccines were granted “approval” in Canada.

“It is important to understand that the COVID-19 vaccines were never approved under the traditional approval process for drugs in Canada,” stated the report (pdf). Instead, Health Canada, the federal agency responsible for national health policy, approved the vaccines through an alternative authorization process—an interim order.

“Under the alternative authorization process, the necessity to establish the safety and efficacy of COVID-19 vaccines through an objective manner appears to have been set aside.”

Canada’s Food and Drug Regulations require that a drug can only be approved in the country after its safety and effectiveness are demonstrated to the Minister of Health. Then, the minister considers whether the benefits outweigh the risks, following which, approval is granted.

Instead of following regulations, the Minister of Health sanctioned an interim order on Sept. 16, 2021, which exempted all COVID-19 vaccines from normal review and approval. This provision usually allows the minister to override normal regulations in situations of “significant risk” to health, safety, or the environment.

In Canada, four COVID-19 vaccines were authorized by the health agency under an interim order—Pfizer-BioNTech, Moderna, Janssen, and AstraZeneca.

The report noted that under the order, vaccines were authorized under a “subjective test.” In this situation, authorization is granted by simply proving that the benefits of vaccination outweigh the risks.

“This cannot be an appropriate standard for approving a drug that the Government intends to administer to the entire population. It is difficult to conceive of a less-scientific test for drug authorization than that found in the Interim Order.”

Moreover, the order made sure that the authorized vaccines could not be revoked even under evidence that it was unsafe and ineffective. Once an interim order is issued, the typical Food and Drug Regulations do not apply.

The order thus exempted manufacturers from having to effectively demonstrate “objective evidence of safety and effectiveness” of their COVID-19 vaccines.

“The result was that while chief medical officers across the country repeatedly assured Canadians that the COVID-19 vaccines were ‘safe and effective’—the general Canadian population had no understanding that their authorization process had not required objective proof of safety nor efficacy.”

‘Not Safe for Human Use’

The NCI report was supported by cardiologist Dr. Peter A. McCullough. “Excellent work @Inquiry_Canada with exhaustive testimony and evidence review. Conclusion: all COVID-19 vaccines unsafe for human use and must be removed from the Canadian market immediately to protect the public,” he wrote in a Sept. 16 post on X.
DALLAS, TX—Peter McCullough, cardiologist, speaks at the Conservative Political Action Conference in Dallas at the Hilton Anatole August 5, 2022. (Bobby Sanchez for The Epoch Times)

Dr. McCullough recently asked European lawmakers to take COVID-19 vaccines off the market due to concerns about illnesses like heart inflammation, blood clots, and neurological diseases.

“COVID-19 vaccines and all of their progeny and future boosters are not safe for human use. I implore you, as a governing body, European Medicines Agency (EMA), to apply all pressure and due urgency to remove the COVID-19 vaccines from market,” Dr. McCullough said in Sept. 13 testimony to the European Parliament.

The NCI report comes as the U.S. Food and Drug Administration (FDA) approved new COVID vaccines on Sept. 11 for children as young as six months old.

“Vaccination remains critical to public health and continued protection against serious consequences of COVID-19, including hospitalization and death,” Dr. Peter Marks, a top FDA official, said in a statement.

However, many experts have questioned the push for new vaccines. Earlier this month, Florida’s Surgeon General, Dr. Joseph Ladapo, criticized the updated shots.

“We all know there’s a new vaccine that’s coming around the corner, [a] new mRNA COVID-19 vaccine. And there’s essentially no evidence ‘for it,” he said during a press conference.

“There’s been no clinical trial done in human beings showing that it benefits people, there’s been no clinical trial showing that it is a safe product for people. And not only that, but then there are a lot of red flags.”

Mr. Ladapo said that mRNA COVID-19 vaccines have “caused cardiac injury in many people."

Not Actually ‘Interim’

Canada’s interim order for COVID-19 vaccines “has become permanent,” according to the NCI report (pdf). An interim order typically only lasts for one year. In March 2022, the order was replaced with permanent regulations which codified the “subjective authorization” of the vaccine.

“Thus, under the permanent test, Health Canada no longer has to be swayed by urgency, but simply by the public health need related to COVID-19. In this way, it seems that so long as COVID-19 is a circulating virus, Health Canada must authorize any vaccine for which there is an argument to support the conclusion that its benefits outweigh its risks,” the report said.

“In effect, we fear that there will never be a need for COVID-19 vaccine manufacturers to prove [the] safety or efficacy of their products.”

NCI also alleged there was a “conflict of interests” while approving the COVID-19 vaccines, with the government being involved.

Political Interests, Letter to Trudeau

Canada usually does not allow drugs to be imported into the country unless approved by Health Canada. However, the interim order allowed the unapproved COVID-19 vaccines to be imported “as long as the Canadian Government was the purchaser,” said the report.

This pre-purchasing and distribution of COVID vaccines were done to make sure the jabs were available for dissemination as soon as they were authorized. “This created a tremendous conflict of interest.”

“Once the vaccines were purchased, imported and ready for distribution, the Government of Canada would have suffered significant political blowback if it was unable to authorize them. Thus, it needed to authorize the COVID-19 vaccines, and it needed to do it quickly.”

The administration “ordered the vaccines, imported them, created new regulations to authorize them, and then took significant measures to convince and coerce every Canadian to take multiple doses. The political stakes were high, and the federal government had every motivation to get the vaccines authorized, regardless of their actual efficacy or safety.”

On Sept. 14, the NCI sent a letter (pdf) to Canadian Prime Minister Justin Trudeau highlighting the issue of COVID-19 vaccine approval.

“Canadians are relying on representations as to the safety and effectiveness of COVID-19 vaccines,” which Health Canada has never determined, the letter said. “Some might draw the conclusion that the misrepresentation to Canadians of proven safety is intentional, made while knowing it to be false and intending it to be relied upon.”

“As a matter of common sense, the objective falsity of the ‘proven safe’ claim brings into question the basis for informed consent to the administration of the injections, creating potentially enormous liabilities.”

In the current context, the organization pointed out that the population immunity has increased along with the latest variants being “milder.”

“In the face of your government’s reported intention to promote booster injections in coming months, the urgency now lies in telling the truth to Canadians and taking corrective action.”

The NCI asked the prime minister to withdraw COVID-19 vaccines “until the normal rigorous evaluation can be completed” and to reinstate the traditional objective test for safety.

"The time for war has not yet come, but it will come and that soon, and when it does come, my advice is to draw the sword and throw away the scabbard." Gen. T.J. Jackson, March 1861
Re: COVID-19 Vaccines Neither Safe, Nor Effective [Re: ConSigCor] #180181
09/20/2023 09:13 AM
09/20/2023 09:13 AM
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‘Statistically Significant Increase’ In Myopericarditis And Single Organ Cutaneous Vasculitis Found After COVID-19 Vaccination

Authored by Megan Redshaw via The Epoch Times (emphasis ours),

A large nationwide study of more than 4 million people in New Zealand identified a statistically significant association in two adverse events following vaccination with Pfizer’s COVID-19 vaccine.
(Fit Ztudio/Shutterstock)

In the post-marketing safety study recently published in Springer, researchers examining 12 specific adverse events found an increase in myopericarditis during the 21-day period following both Pfizer vaccine doses. Myopericarditis describes two distinct inflammatory heart conditions that occur simultaneously, myocarditis and pericarditis.

The highest rate of myopericarditis was observed in the youngest participants under 39 years of age following the second vaccine dose—with an estimated five additional myopericarditis cases per 100,000 persons vaccinated regardless of age. Researchers also observed an increase following both vaccine doses in individuals aged 40 to 59.

“Our findings align with international postmarketing studies, case series reports, and cases detected through reports to New Zealand’s spontaneous system that identify an association between the BNT162b2 vaccine and myo/pericarditis, especially in younger people and after the second dose,” the researchers stated.

In addition to myopericarditis, the study found an increase in single-organ cutaneous vasculitis (SOCV) in the 20- to 39-year-old age group following the first vaccine dose. SOCV is a syndrome characterized by inflammation and damage to the skin’s blood vessels without the involvement of other organ systems.

Study Methods

To carry out their study, researchers collected data from Feb. 19, 2021, at the beginning of the vaccine rollout, to Feb. 10, 2022, among 4,114,364 individuals aged 5 and older who received a first and second primary or pediatric dose of Pfizer’s COVID-19 vaccine. During the study period, 13,597 individuals were excluded after testing positive for COVID-19.

The researchers then compared the incidence rates of each outcome of interest for 21 days—the interval between first and second vaccine doses—following vaccination with Pfizer’s COVID-19 vaccine to the expected background incidence rate from a pre-vaccination period (2014 to 2019) to detect vaccine safety signals.

Outcomes of interest were identified from New Zealand’s National Minimum Data Set—a national data collection system for all public hospitalizations connected to a National Health Index number that allows researchers to link hospitalization with Pfizer vaccination records in the National COVID Immunisation Register.

The 12 adverse events analyzed included acute kidney injury, acute liver injury, Guillain-Barré syndrome, erythema multiforme, herpes zoster, SOCV, myopericarditis (includes all events coded as myocarditis, pericarditis, and myopericarditis), arterial thrombosis, cerebral venous thrombosis, splanchnic thrombosis, venous thromboembolism, and thrombocytopenia.

Outside of myopericarditis and SOCV, researchers identified no other statistically significant associations between Pfizer’s COVID-19 vaccine and other outcomes of interest for all ages combined. Unlike myopericarditis, SOCV has not been identified as an adverse reaction to Pfizer’s COVID-19 vaccine, and only a few case reports and reviews have been published in the literature.

Potential Study Limitations

The study had several potential limitations. Although many adverse events of special interest resulted in hospitalization, some conditions, such as herpes zoster, are typically treated in the primary care setting. Diagnoses of conditions following COVID-19 vaccination in the general setting were not included in the analysis and could be underestimated.

Using ICD-10-AM codes to identify outcomes of interest without conducting clinical record assessments could lead to potential misclassification, and changing diagnostic codes before the study period could overinflate or underestimate potential adverse events.

Healthy vaccinee bias could affect results when comparing observed adverse events among the vaccinated cohort with the background population, as healthier people are more likely to get vaccinated. Additionally, a risk period of one to 21 days may exclude potential adverse events beyond the time frame, according to the study.

Researchers Conclude Benefits of Vaccines Still Outweigh Risks

Despite the increased risk of myopericarditis observed during the study, researchers said the risk of myocarditis following SARS-CoV-2 infection is “substantially greater” than after COVID-19 mRNA vaccination, leading them to conclude the benefits of vaccination still outweigh the risks from the disease.

Yet experts acknowledge that myocarditis caused by a natural viral infection differs from that triggered by mRNA COVID-19 vaccination. As previously reported by The Epoch Times, although COVID-19 can cause myocarditis, the myocarditis developed by a healthy young person post-infection is extremely mild compared to the onset of myocarditis following COVID-19 vaccination.

According to pediatric cardiologist Dr. Kirk Milhoan, myocarditis caused by the COVID-19 vaccine differs from viral myocarditis because an infection of the heart isn’t causing the damage. It’s being damaged by the “spike protein that’s cardiotoxic to the heart,” which causes inflammation in the three main vessels of the heart by a different process.

“There’s a difference between the body encountering a virus naturally that causes myocarditis and actively giving the body something we know causes harm,” Dr. Milhoan told The Epoch Times.

The New Zealand study adds to a growing body of evidence showing mRNA COVID-19 vaccination can trigger heart inflammatory conditions in young people.

"The time for war has not yet come, but it will come and that soon, and when it does come, my advice is to draw the sword and throw away the scabbard." Gen. T.J. Jackson, March 1861
Re: COVID-19 Vaccines Neither Safe, Nor Effective [Re: ConSigCor] #180217
10/04/2023 07:21 PM
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Alarming Covid Jab Contamination Shocks Scientists

By Dr. Joseph Mercola

October 4, 2023

In early April 2023, microbiologist Kevin McKernan — a former researcher and team leader for the MIT Human Genome project1 — posted a preprint paper2 detailing massive DNA contamination in Pfizer’s and Moderna’s bivalent COVID booster shots.3,4,5,6 As explained in the abstract:7

“Several methods were deployed to assess the nucleic acid composition of four expired vials of the Moderna and Pfizer bivalent mRNA vaccines. Two vials from each vendor were evaluated …

Multiple assays support DNA contamination that exceeds the European Medicines Agency (EMA) 330ng/mg requirement and the FDAs 10ng/dose requirements …”

The highest level of DNA contamination found was 30%, meaning nearly one-third of the content of certain vials was plasmid DNA, the presence of which dramatically increases the likelihood of genomic integration and cancer.

What this means, in plain English, is that the shots could potentially alter your DNA, which is something vaccine makers, health authorities and fact checkers have vehemently denied and written off as “impossible.” Yet here we are, with inconvenient facts staring us in the face yet again.

Regulatory Agencies Were Aware of the Problem

In a May 20, 2023, Substack article,8 McKernan pointed out that regulatory agencies were clearly aware of this problem early on, as Pfizer submitted documents to the European Medicines Agency (EMA) showing sampled lots had a broad range of double-stranded DNA (dsDNA) in them.

The EMA’s limit for dsDNA is 330 nanograms per milligram (ng/mg), and Pfizer’s data show sampled lots had anywhere from 1 ng/mg to 815 ng/mg of DNA. And, according to McKernan,9 the EMA’s limit may be too high to begin with, as “lower limits should be applied if the DNA is packaged in transfection ready lipid nanoparticles,” as they are in the shots.

In a sane regulatory environment, this kind of contamination would have resulted in a massive recall, considering the known and suspected dangers of dsDNA contaminants. Yet nothing was done about it.

Since McKernan’s paper was posted, others have confirmed the presence of dsDNA contaminants in the COVID shots. To be clear, DNA should not be present in a commercial product that has been made under good manufacturing practices.

Obviously, Pfizer and Moderna have not perfected their commercial process, or have taken shortcuts they shouldn’t have. As a result, countless millions have been injected with unnecessarily risky COVID shots.

DNA Contamination Confirmed

University of South Carolina professor Phillip Buckhaults has since confirmed the presence of dsDNA in the COVID shots. September 13, 2023, he testified10 to this before the South Carolina Senate Medical Affairs Ad-Hoc Committee on the Department of Health and Environmental Control (DHEC).

Buckhaults is a molecular biologist and cancer geneticist with extensive experience in DNA sequencing, and initially set out to debunk McKernan’s claims. To his shock, he replicated McKernan’s findings instead.

In his testimony, he explained how these DNA contaminants can integrate into your genome and disrupt the function of other genes, either long term or permanently, and may be passed on to offspring for generations.

He told the senators he was “alarmed about this DNA being in the vaccine,” as “there is a very real hazard” of the dsDNA integrating into a person’s genome and becoming a “permanent fixture of the cell” that can result in autoimmune problems and cancers.11

Buckhaults suspects high levels of DNA contaminants may also be causing some of the more serious side effects of the jabs, such as lethal cardiac arrest.12 Of the two lots he analyzed, he found between 5 nanograms and 20 ng of plasmid DNA — ranging from one to 200 base pairs long — per 300 microliter dose, and he points out that having a multitude of tiny fragments is far riskier than having one big piece of DNA.13

The risk of genome integration by dsDNA has been known for decades,14 so the individuals who decided to allow this contamination to remain cannot claim they didn’t know public health would be put at risk.

Buckhaults stressed that we need to collect and analyze DNA from various tissues of those who have received the COVID jabs — at least a few hundred people — to determine whether genomic integration is taking place, and what changes are occurring.

He also explained how the DNA contamination occurred in the first place. In summary, the products used during the clinical trials and the commercial products were not made in the identical way. The commercial product grew the modified RNA using a mix of DNA plasmid and E. coli, and the DNA were not properly filtered out — a clear sign of poor manufacturing processes.

COVID Shots May Cause Cancer in Several Ways

The presence of DNA isn’t the only way in which the mRNA COVID shots can cause cancer. mRNA can also reverse transcribe into DNA under the right circumstances. For example, one in vitro experiment,15,16 published in 2022, demonstrated that the modified RNA in the Pfizer jab has the ability to enter human liver cells and reverse transcribe into DNA in as little as six hours post-exposure. As reported in that peer-reviewed study:17

“… a recent study showed that SARS-CoV-2 RNA can be reverse-transcribed and integrated into the genome of human cells. In this study, we investigated the effect of BNT162b2 on the human liver cell line Huh7 in vitro. Huh7 cells were exposed to BNT162b2, and quantitative PCR was performed on RNA extracted from the cells.

We detected high levels of BNT162b2 in Huh7 cells and changes in gene expression of long interspersed nuclear element-1 (LINE-1), which is an endogenous reverse transcriptase.

Immunohistochemistry using antibody binding to LINE-1 open reading frame-1 RNA-binding protein (ORFp1) on Huh7 cells treated with BNT162b2 indicated increased nucleus distribution of LINE-1 …

Our results indicate a fast up-take of BNT162b2 into human liver cell line Huh7, leading to changes in LINE-1 expression and distribution. We also show that BNT162b2 mRNA is reverse transcribed intracellularly into DNA in as fast as 6 h upon BNT162b2 exposure.”

COVID Jab mRNA Can Enter the Cell Nucleus

According to a 2022 study,18 both the SARS-CoV-2 spike protein and the spike protein mRNA translocated into the nucleus of infected human cells. According to the authors, “the nuclear translocation of both S mRNA and S protein reveals a novel pathogenic feature of SARS-CoV-2.”

If the spike mRNA in the natural virus (and I use that term loosely, considering SARS-CoV-2 was most likely manmade) can enter human cells, might the mRNA in the COVID shots do the same? Probably.

As noted by Buckhaults,19 the lipid nanoparticles that the mRNA and DNA fragments are encased in “facilitate getting the DNA inside the cell — just inside the cell membrane. But once it’s in the cytoplasm, bits of DNA go to the nucleus just by random chance.” He told investigative journalist Maryanne Demasi:20

“We do this in the lab all the time. We take pieces of naked DNA, put them in lipofectamine which is a solution that delivers genetic material into cells, and by magic, some of the pieces integrate into the cellular DNA, and permanently modified the cells.

I’ve been doing this since I was a graduate student, so I know that this happens. The only question is, what is the frequency of this happening across a vaccinated population? …

IF genome modification is happening, It’s just a matter of time before one of these fragments hits a tumor suppressor gene and initiates the beginning of cancer in a single stem cell.

Also, there have been reports of myocarditis. I’m wondering if it’s possible that these little bits of DNA actually encode pieces of the spike protein … There’s a lot of open reading frames in these pieces of DNA that code for peptides that don’t belong in humans and are neo-antigens.

My concern is that some of these pieces of DNA could transform long lived stem cells in, maybe the myocardium, or pericardium, or maybe the liver, or lymph nodes … and now that tissue makes a long-lived expression of some neo-antigen that could be causing a long-term autoimmunity type response like myocarditis.

So, they are the two things that immediately come to mind — the small possibility of cancers in people in the next five years down the road, or the possibility of autoimmunity from the production of these peptides.”

So, the claim that the mRNA in the COVID shots — which is based on but not identical to the spike protein mRNA found in SARS-CoV-2 — cannot enter the nucleus of human cells and therefore cannot be integrated into the human genome, is simply false. Science tells us genome integration can occur in several ways.

COVID Jab Can Have Intergenerational Effects

Another 2022 study21 found that mice injected with the COVID mRNA shot passed on their acquired immune traits — both good and bad — to offspring, which not only suggests that the mRNA can enter the nucleus of the cell, but also that it can be permanently integrated into chromosomal DNA and have intergenerational effects. As reported in this study:

“Hundreds of millions of SARS-CoV-2 mRNA-LNP vaccine doses have already been administered to humans. However, we lack a comprehensive understanding of the immune effects of this platform.

The mRNA-LNP-based [mRNA-lipid nanoparticle-based] SARS-CoV-2 vaccine is highly inflammatory, and its synthetic ionizable lipid component responsible for the induction of inflammation has a long in vivo half-life.

Since chronic inflammation can lead to immune exhaustion and non-responsiveness, we sought to determine the effects of pre-exposure to the mRNA-LNP on adaptive immune responses and innate immune fitness.

We found that pre-exposure to mRNA-LNPs or LNP alone led to long-term inhibition of the adaptive immune response … On the other hand, we report that after pre-exposure to mRNA-LNPs, the resistance of mice to heterologous infections with influenza virus increased while resistance to Candida albicans decreased …

Interestingly, mice pre-exposed to the mRNA-LNP platform can pass down the acquired immune traits to their offspring …

In summary, the mRNA-LNP vaccine platform induces long-term unexpected immunological changes affecting both adaptive immune responses and heterologous protection against infections. Thus, our studies highlight the need for more research to determine this platform’s true impact on human health.”

FDA Responds to DNA Contamination Concerns

McKernan presented his findings to the FDA in June 2023. After Buckhaults confirmed the presence of dsDNA in Pfizer’s and Moderna’s shots, Demasi asked the FDA “if it had begun an investigation into the issue of DNA contamination and whether it would review its guidance to industry about residual DNA in vaccines.”22

She also asked if the agency “had instructed Pfizer and Moderna to conduct further testing to demonstrate the absence or presence of genome modification and whether it would issue new warnings to the public about the potential risks, now that DNA contamination in the vaccines had been established and replicated.” This was the FDA’s response:23

“The mRNA COVID-19 vaccines authorized or approved for use in the United States are not defined as a gene therapy. The FDA is confident in the quality, safety, and effectiveness of these vaccines. The agency’s benefit-risk assessment and ongoing safety surveillance demonstrates that the benefits of their use outweigh their risks.”

In other words, the FDA has taken no action on the matter and has no intention of doing so.

Cancer Promoter Also Found in Pfizer’s Bivalent Jab

In addition to DNA fragments that can more readily integrate into the human genome, and the possibility of mRNA reverse transcribing into chromosomal DNA, McKernan’s team also discovered simian virus 40 (SV40) promoter in the shots, which have long been suspected of causing cancer in humans.24
The SV40 promoter is a sequence used in gene therapy to drive DNA into the nucleus of cells. If the shots aren’t supposed to alter the human genome, why does it contain bits of DNA and an SV40 promoter that can drive that DNA into the nucleus?

SV40 promoter is an oncogenic piece of a virus known to drive very aggressive gene expression for cancer. Combined with pieces of DNA, the presence of SV40 promoter make the risk of cancer all the more likely. What’s more, according to McKernan,25 the SV40 promoter is a sequence used in gene therapy to drive DNA into the nucleus of cells!

If the shots aren’t supposed to alter the human genome, why do they contain bits of DNA and an SV40 promoter that can drive that DNA into the nucleus?

Considering these facts, is it not reasonable to suspect, then, that the “turbo cancers”26 oncologists around are now reporting might indeed be a side effect of the COVID jabs? “Turbo cancer” is an invented term to describe cancers that grow at such unprecedented rates that patients often die before a treatment plan can be implemented.

Repeat Dosing May Promote Cancer and Autoimmune Problems

So, that makes three ways in which some of the shots can contribute to or directly cause cancer. A fourth way the jabs may trigger cancer is simply by repeat dosing. As detailed in a May 2023 paper in the journal Vaccines:27

“To date, 72.3% of the total population has been injected at least once with a COVID-19 vaccine … [I]ncreasing evidence has shown that … they do not produce sterilizing immunity, allowing people to suffer frequent re-infections.

Additionally, recent investigations have found abnormally high levels of IgG4 in people who were administered two or more injections of the mRNA vaccines …

[E]merging evidence suggests that the reported increase in IgG4 levels detected after repeated vaccination with the mRNA vaccines … constitutes an immune tolerance mechanism to the spike protein that could promote unopposed SARS-CoV2 infection and replication by suppressing natural antiviral responses.

Increased IgG4 synthesis due to repeated mRNA vaccination with high antigen concentrations may also cause autoimmune diseases, and promote cancer growth and autoimmune myocarditis in susceptible individuals.”

SV40 Promoter Contamination Confirmed

Buckhaults has also confirmed the presence of SV40 promoter in the plasmid DNA, as has Yusuke Murakami, a professor at Tokyo University. In an interview, Murakami explained:28

“The Pfizer vaccine sequence contains part of the SV40 sequence … This sequence is known as a promoter. Roughly speaking, the promoter causes increased expression of the gene.

The problem is that the sequence is present in a well-known carcinogenic virus. The question is why such a sequence that is derived from a cancer virus is present in Pfizer’s vaccine.

There should be absolutely no need for such a carcinogenic virus sequence in the vaccine. This sequence is totally unnecessary for producing the mRNA vaccine. It is a problem that such a sequence is solidly contained in the vaccine …

If a sequence like this is present in the DNA, the DNA is easily migrated to the nucleus. So it means that the DNA can easily enter the genome. This is such an alarming problem. It is essential to remove the sequence. However, Pfizer produced the vaccine without removing the sequence. That is outrageously malicious.”

Excess Deaths in 2023

If the COVID pandemic was real, we would have seen the highest excess mortality rates in 2020, when the most problematic strain of the virus was in circulation. But that’s not the case. Instead, excess mortality rates didn’t really take off until the rollout of the experimental COVID shots — and rates are still going up, two years later.

In the video above, John Campbell, Ph.D., a retired nurse educator, reviews the latest mortality statistics from the Organization for Economic Co-Operation and Development (OECD).29 He also compares the OECD data with that from Our World in Data, and the two data sets are in agreement — excess deaths continued to be far above normal in 2023, and there’s no pandemic to blame it on.

For the U.K., there were 36,316 excess deaths during weeks 1 through 30 (January 1 through July 30, 202330). A telling trend is that deaths in private homes and “other settings” are above the five-year average, whereas deaths in hospitals and care homes are both below average.31,32

What does that mean? It means that more people than normal are dying unexpectedly, at home and in places other than a hospital. It also suggests that younger people are dying at a higher rate. The higher excess death rate is not because more elderly are dying in care homes.

In the U.S., there were 147,828.8 more deaths than expected during the first 30 weeks of 2023. Other interesting data reveal that, in Minnesota, excess deaths involving blood disorders began in 2020 but then skyrocketed in 2022, nearly doubling from the 2020 rate.33

The original Wuhan strain of SARS-CoV-2 was associated with blood disorders, but that strain had mutated into a mild cold by 2022. What we did have in 2022, however, were the COVID jabs, which are also associated with blood disorders.

Got the Jab? Take Action to Safeguard Your Health

If you already got one or more jabs and now have concerns about your health, what can you do? Well, first and foremost, never take another COVID booster, another mRNA gene therapy shot or regular vaccine. You need to end the assault on your system.

If you developed symptoms you didn’t have before your shot, I would encourage you to seek out expert help. At present, the Front Line COVID-19 Critical Care Alliance (FLCCC) seems to have one of the best treatment protocols for post-jab injuries. It’s called I-RECOVER and can be downloaded from

Dr. Pierre Kory, who cofounded the FLCCC, has transitioned to treating the vaccine injured more or less exclusively. For more information, see Dr. Peter McCullough is also investigating post-jab treatments, which you can find on

The World Health Council has also published lists of remedies that can help inhibit, neutralize and eliminate spike protein, which most experts agree is the primary culprit. I covered these in my 2021 article, “World Council for Health Reveals Spike Protein Detox.”

Sources and References

1, 5 The Healthcare Channel May 22, 2023
2, 7 OSF Preprints April 10, 2023, Edited April 11, 2023 DOI: 10.31219/
3, 28 Twitter KanekoaTheGreat May 20, 2023
4, 8, 9 Anandamide (Kevin McKernan) Substack May 20, 2023
6, 11, 12, 16, 25 Spectator Australia September 25, 2023
10 Jessica Rose Substack September 18, 2023
13, 19, 20, 22, 23 Maryanne Demasi September 21, 2023
14 Ann N Y Acad Sci November 27, 1995; 772: 140-151
15, 17 Curr Issues Mol Biol 2022; 44(3): 1115-1126
18 BioRxiv September 27, 2022 DOI: 10.1101/2022.09.27.509633
21 PLOS Pathogens September 2, 2022 DOI: 10.1371/journal.ppat.1010830
24 Expert Rev Respir Med October 2011; 5(5): 683-697
26 Makis MD Substack June 16, 2023
27 Vaccines (Basel) May 2023; 11(5): 991
29 Organization for Economic Co-Operation and Development Excess Deaths by Week, 2020-2023
30 Week Number Calendar 2023
31 Deaths Registered Weekly in England and Wales Week 36
32 Deaths Registered Weekly in England and Wales Week 37
33 Resisting the Intellectual Illiteratti Substack September 19, 2023

"The time for war has not yet come, but it will come and that soon, and when it does come, my advice is to draw the sword and throw away the scabbard." Gen. T.J. Jackson, March 1861

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