Author Topic: 42.8% greater all-cause mortality in Pfizer's vaccine group than placebo group  (Read 1792 times)

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There is much more to be found on this subject at:
https://childrenshealthdefense.org/

Kennedy's book is a stunning read, and by the time you read just the outrageous content on this page, I've no doubt you will order your copy too.

"The Pfizer Vaccine: A Cold Look at the Shocking Data

(skipping down)

     The final summary of the Pfizer's six-month clinical trial data - the document that Pfizer submitted to FDA to win approval - revealed one key data point that should have killed that intervention forever. Far more people died in the vaccine group than in the placebo group during Pfizer's clinical trials. The fact that FDA nevertheless granted Pfizer full approval, and that the medical community embraced and prescribed this intervention for their patients, is eloquent testimony to the resilience of even the most deadly and inefficacious products, and the breathtaking power of the pharmaceutical industry and its government allies to control the narrative through captive regulators, compliant physicians, and media manipulation, and to overwhelm the fundamental common sense of much of humanity."

"Mathematical Chicanery: Relative Risk vs. Absolute Risk

     On the next page is Pfizer's table S4 that summarized death data from Pfizer's six-month clinical trial. This was Pfizer's final report to FDA; the study by then was unblinded and over. As anyone can see, Pfizer won FDA's approval despite the rather pathetic showing that its vaccine might prevent one COVID death in every 22,000 vaccine recipients.
     So, how did Pfizer transform its unimpressive record of eliminating a single COVID fatality among 22,000 vaccinated subjects into a $5 billion/year success story? By gulling the public with a deceptive measure called "relative risk," instead of the presumptive and far more useful measure of "absolute risk."
     The table shows that during the six-month trial, two people in the placebo group numbering approximately 22,000 and only one in the similarly sized vaccine group died from COVID. Believe it or not, this data point is the source of Pfizer's claim that the vaccine is 100 percent efficacious against death. Since only one person died from COVID in the vaccine group and two died in the placebo group, Pfizer can technically represent that  the vaccine is a 100 percent improvement over the placebo. After all, the number "2" is 100 percent greater than the number "1," right? The media winked at this canard, obligingly reporting Pfizer's extraordinary 100 percent efficacy claim. At least some reporters must have understood that most Americans hearing this statistic would naturally believe that the vaccine would prevent 100 percent of deaths. A more honest - and helpful - way of thinking about the Pfizer vaccine's efficacy is to consider that 22,000 vaccines must be given to save a single life from COVID. Equally concerning, every virologist and infectious disease expert knew that the true reduction in risk of 1/22,000 - or about 0.01 percent, as the BMJ reported - was far too insignificant to make the vaccine even a minor barrier against the spread of COVID. It's axiomatic that any vaccine that does not prevent transmission and that spares only 1 in 22,000 from death from the target contagion has no ability to stop a pandemic. "Because the clinical trial showed that vaccines reduce absolute risk less than 1 percent (See: Brown R. and colleagues from Waterloo in Canada), those vaccines can't possibly influence epidemic curves. It's mathematically impossible," explains Peter McCullough. Nevertheless, Dr. Fauci continued to promote the vaccine as the ultimate panacea.
     The entire justification that Gates and Dr. Fauci had been trumpeting for a year - that their vaccines would end the pandemic - was now so much exploded shrapnel. Nevertheless, Dr. Fauci continued to claim that full vaccination of the entire population was the only way to end the pandemic. He thereby justified his insistence that Americans submit to mass vaccination.
     But the story gets even worse. As table S4 shows, this entire meager advantage of preventing a single COVID death in every 22,000 vaccinated individuals (1/22,000) is entirely cancelled out by a fivefold increase in excess fatal cardiac arrests and congestive heart failures in vaccinated individuals (5/22,000). Pfizer and its regulatory magician, Dr. Fauci, used smoke and mirrors to divert public attention from this all-important question of all-cause mortality.

All-Cause Mortality

"All-cause mortality" should be the key metric in weighing the value of any medical intervention. That measure alone tells us whether vaccinated individuals enjoy better outcomes and longer lives than the unvaccinated. Drugs and vaccines that appear, at first glance, effective against the target disease may, over longer terms, trigger deaths from unexpected causes: accidents, cancers, heart attacks, seizures, even depression and suicide - or from pathogenic priming - which cancel out the short-term benefits of the intervention. As we shall see in the next two chapters, Dr. Fauci learned, at the outset of his career, to find excuses for abbreviating clinical trials of toxic medications to keep long-term mortalities invisible and to cloud overall cost/benefit assessments.
     Pfizer's six-month clinical data for its COVID vaccine trials suggested that, while the vaccine would avert a single death from COVID-19, the vaccinated group suffered 4X the number of lethal heart attacks as the unvaccinated. In other words, there was no mortality benefit from the vaccines; for every life saved from COVID, there were four excess heart attack fatalities. Twenty people died of "all-cause mortality" among the 22,000 recipients in Pfizer's vaccine group, versus only fourteen in the numerically comparable placebo group. (Pfizer was evidently so alarmed by the total number of deaths in its vaccine cohort that it omitted five of them from table S4, and only disclosed them in fine print buried in the body of its report.) That means there were 42.8 percent more deaths in the vaccine than in the placebo groups. Under FDA guidelines, researchers must attribute all injuries and deaths among the study group during clinical trials to the intervention (the vaccine) unless proven otherwise. Under this rule, the FDA must assume people who take the vaccine have a 42.8 percent increased risk of dying.
     This six-month safety report was so damning that it should have closed the case against this vaccine
, but captured FDA officials nevertheless gave Pfizer their approval; the broken VAERS system and the mainstream and social media all conspired to conceal the evidence of the crime when vaccinated Americans began dying in droves, and CDC implemented its own retinue of enshrouding machinations to cloak the real-life carnage."


4:50:50 - Dr. Peter McCullough:  "The vaccines, all the vaccines in use in the United States and predominantly across the world, use genetic technologies that harness the body's own cells to produce the protein on the surface of the virus - the spike protein - which is acknowledged to be dangerous. This is the first time in human medicine that we have an uncontrolled exposure for an uncontrolled duration and quantity in the human body in a mosaic of cells and to make matters worse, the vehicle that carries these genetic products into the human body goes into vital organs. And it's unprecedented that we've ever exposed a single human, let alone hundreds of millions of people to this form of technology. And I published an op-ed before these were ever released saying it was a gamble, I knew it was a gamble, I knew as a clinician and expert in clinical trials in safety that this had a dangerous mechanism of action. It's biologically dangerous and we have seen a large signal on safety, unprecedented numbers of deaths and non-fatal injuries after exposure - we see unprecedented non-fatal injuries in the same data system. And then when we look outside and we look in the yellow card system in the U.K. we see the same thing, and we look in the Eudra system in the E.U., we have just fulfilled the Bradford Hill Tenants of Causality. Meaning, I am telling you as an epidemiologist the vaccines are causing these fatal and non-fatal events to a large degree and many of those around the table I'm sure would agree."

Much more in this stunning read at:
https://childrenshealthdefense.org/

Order your copy of this expose on unbridled evil at your favorite bookseller, or for your convenience at this moment:
"The Real Anthony Fauci: Bill Gates, Big Pharma, and the Global War on Democracy and Public Health (Children’s Health Defense) Hardcover – November 16, 2021"

Kindle version for just $2.99

https://www.amazon.com/Real-Anthony-Fauci-Democracy-Childrens/dp/1510766804/ref=sr_1_1?crid=SKRRZ3I4NVH7&keywords=the+real+anthony+fauci&qid=1643921451&sprefix=the+real+anthony+fauc%2Caps%2C809&sr=8-1
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[edit add 2-21-22] Even the CDC admitted to higher all-cause mortality in Pfizer's vaxx group than placebo, but of course with the standard denial they were vaccine related:

"FDA report finds all-cause mortality higher among vaccinated
FDA report shows Pfizer's clinical trials found 24% higher all-cause mortality rate among the vaccinated compared to placebo group. Report emphasizes that "None of the deaths were considered related to vaccination."
https://www.israelnationalnews.com/news/317091?s=09

Do we have to wonder why the FDA made a request to delay release of Pfizer data until the year 2076?
https://www.covid-19forum.org/index.php?topic=1174.0 [end edit]

Since when were "vaccine" makers allowed relief from the pharmaceutical industry's normal burden of proving that a side effect, injury or death WAS NOT the fault of a drug or vaccine that someone took, but instead their normal burden is transferred to the permanently disabled and survivors of the dead to prove that it was the toxic clot shots that are responsible.
This in spite of the conspicuous volume of vaccine injury, blood clots, myocarditis and exponentially increasing all-cause mortality as evidenced by 2021 life insurance death benefits compared to 2020, are the fault of the clot shots. While even though less than 1% of vaccine injuries are reported to VAERS, these toxic jabs have resulted in triple reports of injury and death than all other vaccine injuries combined since 1990.


« Last Edit: October 26, 2023, 11:14:22 AM by admin »
Over a million Americans have died completely unnecessary, horrific, deaths from COVID-19. Do you have a plan in place to help your family dodge the average $73,300 COVID hospital bill, through prevention and a $20 EARLY treatment protocol? https://www.covidtreatmentoptions.com/

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"Covid-19: Researcher blows the whistle on data integrity issues in Pfizer’s vaccine trial"
https://www.bmj.com/content/375/bmj.n2635

"Pfizer admits in Confidential Documents that its Covid-19 Vaccine may cause Vaccine-Associated Enhanced Disease; and real-world data now proves it definitely does"
https://liputan6.nanyamulu.com/ext-https-dailyexpose.uk/2022/02/03/pfizer-admits-covid-vaccine-causes-ade/

https://duckduckgo.com/?q=pfizer+manipulated+its+vaccine+trial&t=h_&ia=news&iai=https%3A%2F%2Fwww.politico.eu%2Farticle%2Feuropean-medicines-agency-ema-cyberattack-coronavirus-vaccine-data%2F&pn=1

https://peckford42.wordpress.com/2021/08/07/surprise-pfizer-untruthful-berenson/
Surprise—Pfizer Untruthful—Berenson
August 7, 2021 / brianpeckford   

From Alex Berenson now writing on substack

On July 28, Pfizer researchers offered updated results from the company’s pivotal Covid vaccine clinical trial – the 44,000-person study providing the key data supporting use of the vaccine worldwide.

Last week’s report is the final clean update we will ever have on the vaccine’s safety and efficacy. Unless Pfizer is convinced or forced to run another big trial, we will never again have the chance to compare how a large group of people who received the vaccine fared against a matched group who instead received a placebo (no treatment).

Pfizer is responsible for the fact we won’t have good updated data going forward.

It destroyed the chance for longer-term results by offering the vaccine to people who had received the placebo in the trial only days after regulators authorized its use.


In general, to provide useful data, a clinical trial needs two “arms” – people who have gotten a drug or vaccine, and people who haven’t. Only by comparing the arms can we see the differences the treatment has caused.

Pfizer’s trial now has only one arm. Going forward, we will have no way of knowing what we see in terms of infections and side effects – good or bad – comes from the vaccine, broader changes in the epidemic, or other factors.

So the July 28 paper is worth a close read.
https://peckford42.wordpress.com/2021/08/07/surprise-pfizer-untruthful-berenson/
« Last Edit: February 16, 2022, 03:09:55 PM by admin »
Over a million Americans have died completely unnecessary, horrific, deaths from COVID-19. Do you have a plan in place to help your family dodge the average $73,300 COVID hospital bill, through prevention and a $20 EARLY treatment protocol? https://www.covidtreatmentoptions.com/

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https://www.israelnationalnews.com/news/317091?s=09

"FDA report finds all-cause mortality higher among vaccinated
FDA report shows Pfizer's clinical trials found 24% higher all-cause mortality rate among the vaccinated compared to placebo group.
Report emphasizes that "None of the deaths were considered related to vaccination.
David Rosenberg  17.11.21 13:51

The clinical trials of Pfizer’s coronavirus vaccine found that the all-cause mortality rate of the vaccinated group was higher than that of the control group, months after the trials were launched, according to a recently released FDA report.

According to the report, which was released by the US Food and Drug Administration to provide background information on its August 2021 decision to grant full approval for the Pfizer-BioNTech coronavirus vaccine after offering limited emergency authorization of use in last December, six months after the vaccine’s clinical trial began, the total number of deaths reported in the vaccinated group was nearly one-quarter higher than the number of deaths in the placebo group.

Is there extra panic regarding the new Covid strain? Read the latest Op-ed.

The report emphasized that "None of the deaths were considered related to vaccination."

Just under 22,000 participants were included in each group, with half receiving the coronavirus vaccine, and half receiving a saline solution injection.

The initial results of the clinical trials suggested a high-level of efficacy for the vaccine in preventing symptomatic cases of COVID-19, an in particular, serious illness from COVID – but lacked significant data on all-cause mortality, due to the short time-frame and small number of total deaths.

A follow-up assessment of participants completed on March 13th of this year looked at the overall health outcomes of the trial participants, six months after they received either the COVID vaccine or the saline solution injection.

While Pfizer in July released partial data on the outcomes from the six-month assessment ending March 13th, the new FDA report includes more comprehensive data, and shows a significantly higher number of all-cause fatalities among the vaccinated cohort.

The Pfizer report in late July of this year showed effectively equal all-cause fatality rates between the vaccine and placebo cohorts six months after the tests were conducted, with 15 deaths among the nearly 22,000 vaccine recipients, versus 14 deaths among the nearly 22,000 placebo recipients.

Most of the total 29 deaths in both groups were not related to the coronavirus; of the deaths in both groups, three fatalities were listed as being related to the virus; two in the placebo group and one in the vaccinated group.

The FDA report, however, revealed a larger number of deaths by all causes in both groups, with 17 deaths among the control group and 21 in the vaccinated cohort.

The relative difference in all-cause deaths between the two cohorts amounts to 23.5%, though the absolute number of deaths was small – 38 total for all participants in the trial.

However, the FDA justifying its August 2021 approval for the vaccine did not find a link between the vaccine and increased mortality risk, noting that the majority of side-effects, and all common side effects (any reported by more than 10% of recipients) were mild, ranging from fatigue and headache to muscle pain, chills, joint pain, fever, and swelling.

The total number of serious adverse events reported among the placebo and vaccine group were comparable, with 103 events reported among the vaccine group and 117 among the control group, though a break-down and comparison of serious adverse events was not provided.

The FDA report also said that during its initial assessment of the vaccine, no notable patterns linking the vaccine in a 'causal relationship' to specific adverse outcomes were found.

However, the report did say that following the issuance of the emergency use authorization in December 2020, a number of cases of rare heart conditions, including myocarditis and pericarditis, were reported following vaccination, leading the FDA and CDC to identify "serious risks for myocarditis and pericarditis following administration of" the Pfizer vaccine. The risk factor appears to be higher in males under 40, the report added, with boys ages 12 to 17 being especially at risk."
« Last Edit: February 16, 2022, 03:06:24 PM by admin »
Over a million Americans have died completely unnecessary, horrific, deaths from COVID-19. Do you have a plan in place to help your family dodge the average $73,300 COVID hospital bill, through prevention and a $20 EARLY treatment protocol? https://www.covidtreatmentoptions.com/

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"Edward Dowd: Pfizer’s Covid-19 vaccine should have been “dead on arrival” because it failed “all-cause mortality endpoint.”
https://ragnarforseti.substack.com/p/edward-dowd-pfizers-covid-19-vaccine?s=r

"Edward Dowd: COVID Vaccines Are "The Greatest Fraud In History"
https://rumble.com/embed/vv3cy4/?pub=4
https://rumble.com/vxpj02-edward-dowd-covid-vaccines-are-the-greatest-fraud-in-history.html

British Medical Journal:  "BMJ Investigation
Covid-19: Researcher blows the whistle on data integrity issues in Pfizer’s vaccine trial
"
https://www.bmj.com/content/375/bmj.n2635
_________________________________

"Pfizer Whistleblower Brook Jackson Sues Pfizer For $2 Billion Over Falsified mRNA Data Submitted To Obtain FDA Authorization For COVID-19 'Vaccines'

Defendants Pfizer Inc, Ventavia Research Group & ICON "deliberately withheld crucial information from the United States that calls the safety and efficacy of their vaccine into question."
ragnar_forseti
Feb 19

A former clinical trial overseer for a contractor holding trials of Pfizer’s COVID-19 vaccine is pressing forward with a lawsuit against Pfizer and her former company despite the U.S. government declining to side with her.

Brook Jackson was fired by the contractor, Ventavia Research Group, in 2020. She came forward as a whistleblower in 2021."

"A former clinical trial overseer for a contractor holding trials of Pfizer’s COVID-19 vaccine is pressing forward with a lawsuit against Pfizer and her former company despite the U.S. government declining to side with her.

Brook Jackson was fired by the contractor, Ventavia Research Group, in 2020. She came forward as a whistleblower in 2021."

"Government lawyers did not explain the choice not to intervene and the Food and Drug Administration (FDA), which investigates alleged clinical trial fraud, did not respond to a request for comment.

The choice, though, has not deterred the whistleblower.

“We’re going to pursue the case without the help of the government,” Jackson told The Epoch Times.

She said she wasn’t surprised but felt “total disappointment” when, after over a year of putting off a decision, the government declined to intervene.

The odds of success aren’t good but “it’s just a chance I have to take,” Jackson said. “I just feel like somebody has to be held accountable.”

Jackson set off a firestorm when the British Medical Journal in November 2021 published a piece, based on documents, recordings, and other materials from Jackson, that outlined repeated failures by Ventavia to properly run sites for Pfizer’s COVID-19 vaccine trial before it received emergency clearance from U.S. drug regulators."
https://www.bmj.com/content/375/bmj.n2635
______________________________________________

"Who is Brook Jackson? Whistleblower Leaves 20% Dent on BioNTech Shares on Single Day"
https://www.ibtimes.sg/who-brook-jackson-whistleblower-leaves-20-dent-biontech-shares-single-day-61120
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« Last Edit: May 25, 2022, 01:11:17 PM by admin »
Over a million Americans have died completely unnecessary, horrific, deaths from COVID-19. Do you have a plan in place to help your family dodge the average $73,300 COVID hospital bill, through prevention and a $20 EARLY treatment protocol? https://www.covidtreatmentoptions.com/

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So no surprise to learn that:

"Oh what a tangled web pharma weaves with its arbiters of vaccine safety. Appointed in secret, meeting in secret, identities kept secret, and all paid by the companies they are supposed to oversee. What could possibly go wrong?!

ICAN’s attorneys have done some more digging since we warned in 2020 that the Data and Safety Monitoring Boards (DSMBs) overseeing vaccine trials were compromised by financial ties to Big Pharma. Now, thanks to the dogged FOIA efforts of ICAN’s attorneys to research documents produced from Pfizer’s biological product file, we see just how deep the corruption goes.

Among the latest cache of documents extracted from the FDA is a 61-page document, entitled Investigational BNT162 Vaccine Program, which describes Pfizer’s internal-review mechanism for the Covid-19 vaccine trials it conducted in 2020 and 2021. Pages 51 and 52 list five original members of Pfizer’s ‘External Data Monitoring Committee’ (EDMC), its own DSMB, with two more members added in February 2021. (Interestingly, these two members are both Maternal Fetal Medicine doctors).

Of the original five members, we knew of one early on because a CBS article revealed in September 2020, apparently by mistake, the inclusion of Kathryn Edwards, MD, a professor at Vanderbilt University. In case you missed our earlier briefing about her, here’s a brief recap: She was a paid advisor to Pfizer directly before joining the DSMB. She has also received payments, speaking fees, or funding from numerous pharmaceutical companies, including Moderna, Merck, and Smith-Kline Beecham, while Sanofi provided her with trips to Paris, Dublin, Amsterdam, and Cancun, among other destinations. Nice work if you can get it!

But surely she would be forthcoming about all such connections, right? Well, in her July 2020 presentation to the Advisory Committee on Immunization Practices (ACIP), titled COVID'19 Vaccine Safety Considerations, the conflict conveniently was never disclosed despite the fact that she had been on a COVID-19 DSMB for over 3 months at that point!

Now, we finally have the names of the other DSMB members too. But before we look at them, here’s a reminder of what NIAID director Anthony Fauci, told an interviewer in September 2020. The DSMBs, he said, are “beholden to no one, not to the president, not to the vaccine companies, not to the FDA. Not to me.”

Well, this certainly doesn’t stand up in the case of Kathryn Edwards, but how accurate is Fauci’s pronouncement when it comes to the other members of Pfizer’s DSMB reviewing vaccine trial data? Here’s a thumbnail sketch:

Jonathan Zenilman, MD, of Johns Hopkins University, was the chair of the committee. He received consulting fees from Pfizer in every year from 2014 to 2020 to the tune of $78,279 ($28,168 in 2020 alone). Beyond that, he received $6,045.09 in compensation from being wined and dined, and travelling at Pfizer’s expense between 2014 and 2019. His other Big Pharma patrons over these years include GSK, Merck, Smith & Nephew, Cubist, Siemens Medical Solutions, Cipla, Tetraphase Pharma, The Medicines Company, K2M, Becton, Dickinson and Company, Perrigo, and Theravance. Between 2014 and 2020, Dr. Zenilman received an astonishing $91,257.69 from these pharmaceutical companies (including Pfizer) excluding research funding. In addition, Zenilman has received NIH funding.

Robert Belshe, MD, founder of the Center for Vaccine Development at Saint Louis University School of Medicine, received various consulting fees and compensation from Pfizer, GSK, Dermira, Sanofi, AstraZeneca, Merck, Emergent Biosolutions, Comsort, Seqirus, Novartis, and Viiv Healthcare during every year from 2014 to 2020, and from AstraZeneca every year from 2014 to 2018. “How much” you ask? An incredible total of $452,794.26, excluding research funding. Pfizer was especially forthcoming with consulting fees, speaking fees, and generous helpings of “Food and Beverage” and “Travel and Lodging,” compensating him $36,225 in 2020 alone. Dr. Belshe disclosed his own conflicts in a 2019 article: Belshe has been a consultant and/or speaker for GSK, Medimmune, Sanofi, Flugen, Novavax, Merck, and Moderna; owns stock/stock options in Flugen; is a scientific board member for Flugen; and has served on data safety monitoring board for GSK, MedImmune, Vical, and Vaxart.

Lawrence Stanberry, MD, of Columbia University, received more than $23,000 from Pfizer in 2020, as well as research funding from the NIH, CDC, and the Bill and Melinda Gates Foundation.   He reports consulting fees from Janssen, GSK, and Novartis and is a member of the scientific advisory board of Abivax. Nothing to see here!

Robert Philips Heine, MD, of Wake Forest Baptist Health in Winston-Salem, NC, received $27,450.28 in payments from pharmaceutical companies between 2014 and 2020 for travel and lodging, food and beverage, and consulting fees. Pfizer provided the bulk of these payments with $4,812.50 for consulting fees in 2020 alone. Heine has been a consultant and speaker for GSK and Merck and has received research funding from GSK. His work has been funded by the Bill and Melinda Gates Foundation.

Heather S. Lipkind, MS, MS, of Yale School of Medicine, accepted consulting fees and research funding from Pfizer during 2019 and 2020, for a total of $21,660.

Steve Self, PhD, a statistician at the Fred Hutchinson Cancer Research Center, is also a board member of Health Stream Analytics, an organization developing “novel easy-to-use biometric sensors.”

We’ve said it before, but now we’re saying it again, and louder: the individuals involved with overseeing and green-lighting Covid-19 injections are a cozy club of insiders whose pockets are now further richly lined with Big Pharma spoils.

To share this legal update, please use this link: https://www.icandecide.org/ican_press/conflicts-of-interest-in-pfizer-vaccine-trial/
« Last Edit: October 03, 2022, 03:20:06 PM by admin »
Over a million Americans have died completely unnecessary, horrific, deaths from COVID-19. Do you have a plan in place to help your family dodge the average $73,300 COVID hospital bill, through prevention and a $20 EARLY treatment protocol? https://www.covidtreatmentoptions.com/

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https://grandsolarminimum.com/2022/12/01/covid-19-vaccine-harm-evidence/#_Toc121035137

"Open Letter & Evidentiary Document sent to the New Zealand Prime Minister and Ministers

by Carlton Brown | Dec 1, 2022 | 3 comments

Download a copy of the: (1) evidentiary document referred to in this Open Letter (PDF: EvidentiaryDocument_COVID19NationalLevelHarm_01122022, MS Word (clickable citations): EvidentiaryDocument_COVID19NationalLevelHarm_01122022), (2) associated study results and graphics (ADE_VAED_Vaccine-failure), (Toxic COVID-19 vaccine Lots (VEARS, USA))"

Dear Rt Hon Jacinda Ardern, Prime Minister, Hon Andrew Little, Minister of Health, Hon Dr. Ayesha Verrall, Minister of COVID-19 Response, and Hon Peeni Henare and Hon Aupito William Sio, Associate Ministers of Health

In this Open Letter and evidentiary document, I share my research results on overseas government and Ministry of Health (MoH) COVID-19 vaccine surveillance and pharmacovigilance data indicating irreparable vaccine-induced harm. Furthermore, I share important evidence that SARS-CoV-2 originated from gain-of-function research, remind you that no evidence exists for an animal-to-human origin, and highlight that its potential source lay beyond Wuhan, China. A series of requests for investigations are made below linked to this evidence, including the statistical biases evident in the Ministry of Health and other healthcare agencies’ calculable unvaccinated COVID-19 case rates. These biases essentially eliminated the negative vaccine effectiveness harm signal from ready public view. This evidentiary document is provided by a former European corporate venture capital-funded CEO/vaccine innovator (“Vaccines for Mutating Viruses”), veterinarian with 36 years of vaccine use experience, and a private researcher. It is supported by 525 unique data, scientific, and other citations.

According to New Zealand, England, Scotland, and Canada healthcare agencies and Global surveillance data (77 nations), these vaccines failed to prevent SARS-CoV-2 infection as initially touted. Significant negative vaccine effectiveness and vaccine failure were evident with the emergence of antigenically distinct strains (i.e., Delta, Omicron). The vaccine industry experienced antibody-dependent enhancement of virus infection (ADE) and vaccine-associated enhanced disease (VAED) with three other different coronaviruses and their spike protein vaccine prototypes in the last 30 years, giving my study results a predictable context. Furthermore, one year of US lot-numbered COVID-19 vaccine-associated deaths and hospitalizations equaled 32x (Comirnaty 15.4x) and 20x (Comirnaty 10.5x) of all US vaccine-associated deaths and hospitalizations, respectively. These adverse outcomes were highly skewed and peaked across vaccine lots and were associated with a minority of lots sent to a larger number of US States. This data highlights that there was an urgent need for investigation by the US and other regulatory and healthcare agencies before expanded population use.

A vast chasm exists between the vaccine safety and efficacy experienced in 2021-2022 and the falsifiable 95% vaccine efficacy and safety proclaimed by governments with Comirnaty’s first Emergency Use Authorization in 2020 (USA). This document reviews critical pharmacotoxicology and clinical safety package deficiencies evident in overseas regulatory reviews. This helps explain why Pfizer then struggled to cope with the sheer volume of Comirnaty adverse event reports in the first 90 days post-launch. This was uncharacteristic of a safe vaccine. Numerous vaccine-associated enhanced disease mechanisms are evident by which vaccine spike proteins can cause disease or exacerbate comorbidities common to severe COVID-19 outcomes. These mechanisms place upregulated furin and angiotensin-converting enzyme-2 receptors (ACE2) and prevalent comorbidities in tissues and organs common to all three center-stage. At the same time, SARS-CoV-2’s spike protein provides its uniquely encoded furin cleavage site for the furin to cleave its S1 and S2 sub-units and activate its ACE2-receptor-mediated infectivity and pathogenicity.

Of grave concern for global public health is a gain-of-function origin to SARS-CoV-2 is indicated by its spike protein incorporating human infectivity and pathogenicity enhancing features unprecedented in nature while synthetic biology left its fingerprints. Furthermore, there is no evidence supporting a Wuhan Huanan market zoonosis because no virus progenitor or animal host was ever identified. There are two reasons for detailing a coronavirus gain-of-function origin to SARS-CoV-2. Firstly, the negative vaccine effectiveness evident in governments’ COVID-19 surveillance data could have been enhanced by a genetically modified SARS-CoV-2. Secondly, the world will be left vulnerable to future pandemics if there was no accidental release from the Wuhan Institute of Virology. At least two other potential SARS-CoV-2 origins exist beyond Wuhan, with one of these potentially involving a WHO, Five Eyes, and NATO-spearhead member nation connected with Ukraine.

The US Department of Defense (DoD) and National Institutes of Health (NIH) funding of EcoHealth Alliance (EHA, $69 million) and its connections one-degree-removed were scrutinized because EHA’s leader led a failed attempt to cover up SARS-CoV-2’s gain-of-function origin. EHA directed research that genetically modified bat SARSr-CoVs that could not infect humans so that they could. EHA’s $14.2 million funding application to the DoD in 2018 showed its intent to insert a codon-optimized furin cleavage site (FCS) into bat SARSr-CoVs. A uniquely encoded Arginine-doublet containing FCS now sits between SARS-CoV-2’s spike protein S1 and S2 sub-units, which has no precedent in known viruses and may have infringed patents. Besides EHA’s long-standing collaborations with two coronavirus gain-of-function research epicenters in the USA and China, it had another with Metabiota. Metabiota’s Series-A lead investor was a Hunter Biden part-owned investment firm. The DoD-funded Metabiota operated in Pentagon Biolabs in Ukraine and US-funded Biolabs in Cameroon and researched corona-, monkeypox-, influenza-, and Ebola viruses. Metabiota has implemented major DoD and Homeland Security contracts across Central Africa while its surveillance role in Sierra Leone’s Ebola outbreak in 2014 created significant controversies.

You are requested to investigate: (1) this New Zealand and overseas evidence for negative vaccine effectiveness, vaccine failure, and toxic vaccine lots, (2) the statistical biases evident in the MoH and other healthcare agencies’ calculable unvaccinated COVID-19 case rates, which essentially eliminated the negative vaccine effectiveness signal, (3) the role of COVID-19 vaccination in exacerbating comorbidities most frequently associated with serious-severe COVID-19 outcomes, (4) SARS-CoV-2’s gain-of-function origin while internationally championing a punitive global ban on gain-of-function R&D, and (5) the conduct of the WHO during COVID-19 linked to seven critical points detailed in section 2.7. Would you please ensure New Zealanders are updated on their recently acquired life-long health risks and that informed consent guidelines associated with COVID-19 vaccination be urgently amended? Would government please prioritize clinical research into COVID-19 antibody-dependent enhancement of virus infection, vaccine-associated enhanced disease, and antigenic imprinting in the New Zealand population? Thank you.

Yours sincerely

Dr. Carlton Brown BVSc (1986, Massey University), MBA (1997, London Business School).

Former CEO and co-innovator at Immune Targeting Systems Ltd (UK), “Vaccines for Mutating Viruses.”

Raising awareness for antibody-dependent enhancement of virus infection (ADE), vaccine-associated enhanced disease (VAED), and antigenic imprinting.

https://www.linkedin.com/in/carlton-brown-13b66232/, https://orcid.org/0000-0003-4871-7521, https://gettr.com/user/covid19_ade_vaed.

Download the Open Letter and Evidentiary Document: https://grandsolarminimum.com/2022/12/01/covid-19-vaccine-harm-evidence/."
https://grandsolarminimum.com/2022/12/01/covid-19-vaccine-harm-evidence/#_Toc121035137
« Last Edit: December 07, 2022, 07:47:25 AM by admin »
Over a million Americans have died completely unnecessary, horrific, deaths from COVID-19. Do you have a plan in place to help your family dodge the average $73,300 COVID hospital bill, through prevention and a $20 EARLY treatment protocol? https://www.covidtreatmentoptions.com/

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https://www.lifesitenews.com/news/fda-quietly-discloses-that-21-not-15-people-died-during-pfizers-jab-trials/

"FDA quietly discloses that 21, not 15, people died during Pfizer’s jab trials
The new data shows that those who received Pfizer’s treatment during the clinical trial died in greater numbers than those who received a placebo.

 Mon Nov 22, 2021 - 12:36 pm EST

Help Angelia recover from Vax Injury: LifeFunder.com

SILVER SPRING, Maryland (LifeSiteNews) – The FDA has quietly released a statement stating that 21 people died during Pfizer’s COVID-19 vaccine clinical trial, significantly more than the company publicly reported.

On November 8, the Food and Drug Administration (FDA) released a 30-page statement entitled “Summary Basis for Regulatory Action” to explain the rationale behind approving the Pfizer COVID-19 so-called vaccine. The report stated that 21 people in the vaccine recipient group died between November 2020 and March 2021, but the pharmaceutical company told the public in July that only 15 people had died during that period. 

“Pfizer said publicly in July it had found 15 deaths among vaccine recipients by mid-March. But it told the FDA there were 21 – at the same data cutoff end date, March 13,” wrote Alex Berenson, a former New York Times reporter and bestselling author, in his analysis of the latest information. 

“Could the discrepancy result from some odd data lag? Maybe, but the FDA briefing book also contains the number of Covid cases that Pfizer found in vaccine recipients in the trial. Those figures are EXACTLY the same as those Pfizer posted publicly in July. Yet the death counts were different,” he added. 

“Pfizer somehow miscounted – or publicly misreported, or both – the number of deaths in one of the most important clinical trials in the history of medicine.”

To make matters worse for the FDA’s safety claims, with 21 deaths in the group of 22,000 who received the shot, and only 17 deaths in the placebo group of 22,000 who received a benign saline shot instead, the new data shows that those who received Pfizer’s treatment died in greater numbers than those who did not. Nevertheless, the experimental injections were still approved for widespread use."
« Last Edit: February 19, 2023, 11:30:24 AM by admin »
Over a million Americans have died completely unnecessary, horrific, deaths from COVID-19. Do you have a plan in place to help your family dodge the average $73,300 COVID hospital bill, through prevention and a $20 EARLY treatment protocol? https://www.covidtreatmentoptions.com/

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Even worse, the vaccine rolled out was not the same as the one from the trials, because it has been grown on bacteria.
https://twitter.com/i/status/1706653151439507954
« Last Edit: October 03, 2023, 12:56:06 PM by admin »
Over a million Americans have died completely unnecessary, horrific, deaths from COVID-19. Do you have a plan in place to help your family dodge the average $73,300 COVID hospital bill, through prevention and a $20 EARLY treatment protocol? https://www.covidtreatmentoptions.com/