Study: 70% of deaths linked to Pfizer COVID-19 vaccine in Japan were reported within 10 days of vaccination

A peer-reviewed Japanese study published in the journal Cureus has revealed that around 70 percent of people who died in Japan after receiving the Pfizer’s Wuhan coronavirus (COVID-19) vaccine passed away within the first 10 days after vaccination.

In the study, researchers examined the link between Pfizer COVID-19 vaccination and deaths within 10 days of vaccination. The research team defined the risk period as within 10 days of vaccination, with vaccination day being Day 1, and the control period defined as 11 to 180 days following vaccination.

The analysis was divided into two groups: Group 1 included volunteers aged 65 and above and Group 2 included people aged 64 and younger.

The scientists reported that there were 1,311 deaths in Group 1, which was made up of 662 adult men and 649 adult women. In Group 2, they identified 247 deaths, 155 males and 92 females.

Findings revealed that the percentage of reported cases that experienced death within 10 days after COVID-19 vaccination was “71 percent in Group 1 and 70 percent in Group 2.” In Group 1, more women than men died overall due to different medical conditions in the first 10 days of vaccination. After 10 days, there were more deaths reported among the males.

Many of the post-vaccine deaths occurred on day one, followed by the third and fourth days. (Related: COVID-19 vaccine data administrator reveals deaths related to bad batch of Pfizer shots.)

Autopsies were performed in just eight of the 239 unexplained death cases. Aside from these unknown deaths, the biggest causes of mortality in the over 65s were ischemic heart disease with 119 deaths, heart failure with 92 deaths and aspiration pneumonia or asphyxia with 72 deaths.

In Group 2, over twice the number of men died than women from different medical conditions within the first 10 days of vaccination. Overall deaths after the initial 10 days were only a little higher among the men. The highest number of post-vaccination deaths was recorded on the third day, followed by the fourth, second and fifth days.

Only nine of the 51 reported “unexplained deaths” had autopsies. After unexplained deaths, the biggest causes of death in Group 2 were ischemic heart disease with 27 deaths, cardiac arrhythmias with 24, subarachnoid hemorrhage with 20 and myocarditis or pericarditis with 17 deaths.

Findings also revealed that there was a significant difference in male and female deaths due to myocarditis or pericarditis during the “risk period,” with eight men dying compared to one woman. Additionally, heart failure resulted in the deaths of nine men compared to two women.

Researchers reported that some of the myocarditis or pericarditis cases “may be included within the unexplained deaths category,” adding that myocarditis is a complication of vaccination, especially in young adults and adolescent males.

One contributing factor for higher deaths of men during the first 10 days is believed to be the high number of myocarditis or pericarditis deaths including undiagnosed cases.

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An explosive new study describing “unintended immune responses” from mRNA injections has dropped a tactical nuke on Pfizer

Pfizer must feel like it’s been one damned thing after another these days. In a year packed with horrible news for the jabs – not to mention poor jab recipients – yesterday saw a critical new discovery of jab problems, possibly the worst and most damning yet. How bad was it? It was so bad that, even though I almost never make predictions any more, I will predict this: The FDA will be forced to withdraw the mRNA covid shots because of this study.

I’m not even joking about that.

Our investigation begins with yesterday’s Telegraph article about a new study headlined: ‘One in four who had Moderna or Pfizer Covid jabs experienced unintended immune response’.

The explosive, new, peer-reviewed, gold-standard study is already making news even though it was only published yesterday, 6 December. And it published in the well-respected journal Nature, featuring the multisyllabic, incomprehensible title, ‘N1-methylpseudouridylation of mRNA causes +1 ribosomal frameshifting’.

This study has twenty authors. There is safety in numbers.

Don’t let the mind-numbing title fool you. If Kevin McKernan’s SV40 monkey virus discovery tossed a hand grenade into Pfizer’s machine-gun bunker, this carefully-written study dropped a tactical nuke on Pfizer’s Pacific Fleet anchoring at Hawaii. The study’s implications are vast.

Since the science is a little thick – no, it’s very thick – I’ll start by telling you the end first.

Here’s how The Telegraph’s article defensively described the study’s results. Keep in mind, they were down-playing the results, as much as they possibly could:

No adverse effects were created by the error, data show, but Cambridge scientists found such vaccines were not perfect and sometimes led to nonsense proteins being made instead of the desired Covid “spike”, which mimics infection and leads to antibody production (and) an immune system flare-up.

The new study, published in Nature, found this occurred in around 25-30 per cent of people.

Hahaha! The vaccines were “not perfect!!” Oh my gosh! Please, stop! Hahahaha! It hurts to laugh! Whew. Alright, I’m okay now. Onwards.

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Pfizer ‘Knowingly Distributed’ Adulterated Drugs to Children: Lawsuit

Pfizer and one of its partners distributed a medication to children despite having knowledge that the drug was adulterated, according to legal action unsealed on Nov. 20.

Pfizer and Tris Pharma distributed Quillivant XR, a drug for children aimed at treating attention-deficit/hyperactivity disorder (ADHD), even though the companies knew the drug did not meet federal standards, the lawsuit from Texas Attorney General Ken Paxton says.

The U.S. Food and Drug Administration (FDA) approved Quillivant in 2012 but soon after its approval, the drug failed quality control tests, according to the suit.

Instead of investigating the root cause, as required by federal rules, Tris repeatedly changed testing methods allegedly to try to generate positive results, Mr. Paxton’s probe found. Tris was “under financial pressure” to “rapidly increase production” and did ramp up production but “without adequate controls,” the suit states.

Quillivant comes in powder form and is reconstituted by pharmacists with water.

The medication is a schedule II controlled dangerous substance, and suppliers are required by the FDA to ensure display of a black box warning about abuse and dependence, and the potential side effects which include nausea, vomiting, and insomnia. It was developed by Nextwave Pharmaceuticals, and was acquired by Pfizer in May 2012.

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How Pfizer Hid Nearly 80% of COVID Vaccine Trial Deaths From Regulators

Pfizer-BioNTech delayed reporting vaccine-associated deaths among BNT162b2 clinical trial participants until after the U.S. Food and Drug Administration (FDA) issued an Emergency Use Authorization (EUA) for the product.

The vaccine makers also failed to account for a large number of subjects who dropped out of the trial.

Together, these strategies kept regulators and the public ignorant of a 3.7-fold increase in cardiac deaths among subjects who received the vaccine, according to analysis in the International Journal of Vaccine Theory, Practice, and Research.

The authors of the paper described it as a “forensic analysis,” defined by the U.S. National Institute for Standards and Technology as “the use of scientific methods or expertise to investigate crimes or examine evidence that might be presented in a court of law.”

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Researchers Alarmed to Find DNA Contamination in Pfizer Vaccine

Phillip Buckhaults, a cancer genomics expert, and professor at the University of South Carolina has testified before a South Carolina Senate Medical Affairs Ad-Hoc Committee saying that Pfizer’s mRNA vaccine is contaminated with billions of tiny DNA fragments.

Buckhaults, who has a PhD in biochemistry and molecular biology, said “there is a very real hazard” that these fragments of foreign DNA can insert themselves into a person’s own genome and become a “permanent fixture of the cell.”

He said it’s a plausible mechanism for what might be “causing some of the rare but serious side effects like death from cardiac arrest” in people following mRNA vaccination.

Buckhaults is not an alarmist and has been reluctant to go public with his findings for fear of frightening people.

He himself was vaccinated three times with Pfizer’s covid vaccine and recommended it to family and friends. He described the mRNA platform technology as “revolutionary” and said the vaccine has saved many lives.

“I’m a real fan of this platform,” Buckhaults told the Senate. “I think it has the potential to treat cancers, I really believe that this platform is revolutionary. In your lifetime, there will be mRNA vaccines against antigens in your unique cancer. But they’ve got to get this problem fixed.”

Buckhaults is most concerned about the “very real theoretical risk of future cancer in some people, depending on where this foreign piece of DNA lands in the genome, it can interrupt a tumour suppressor gene or activate an oncogene.”

“I’m kind of alarmed about this DNA being in the vaccine… DNA is a long-lived information storage device. It’s what you were born with, you’re going to die with and pass on to your kids. … So alterations to the DNA…well, they stick around,” he said.

Buckhaults believes the vaccines were deployed in good faith, but given the panic and urgency of the crisis, “there were a lot of shortcuts taken.” He puts it down to incompetence not malice, quoting Hanlon’s razor

“…. which is never attribute malice to that which can be better explained by incompetence. There could be malice underneath, but I’m trying to see just incompetence to be gracious,” he told the Senate.

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Pfizer Vaccine Batches in the EU Were Placebos, Say Scientists

Scientists have uncovered startling evidence that a substantial portion of the batches of the Pfizer-BioNTech COVID-19 vaccine deployed in the European Union may in fact have consisted of placebos – and that the German regulator knew this and did not subject them to quality-control testing.

The scientists, Dr. Gerald Dyker, Professor of Organic Chemistry at the Ruhr University Bochum, and Dr. Jörg Matysik, Professor of Analytical Chemistry at the University of Leipzig, are part of a group of five German-speaking scientists who have been publicly raising questions about the quality and safety of the BioNTech vaccine (as it is known in Germany) for the last year and a half.

They recently appeared on the Punkt.Preradovic online programme of the German journalist Milena Preradovic to discuss batch variability. Their starting point was the recent Danish study showing enormous variation in the adverse events associated with different batches of the Pfizer-BioNTech vaccine, or BNT162b2 per its scientific codename. The below figure from the Danish study illustrates this variation.

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FDA Reveals Rare, Possibly Fatal Neurological Disorder Is A “Potential Risk” With New Pfizer Vaccine

People around the globe have suffered serious adverse reactions resulting from COVID vaccines, especially from the Pfizer shot.

Now the Food and Drug Administration (FDA) tells us another Pfizer vaccine can cause serious complications in recipients. After receiving Pfizer’s Respiratory Syncytial Virus (RSV) shot during a clinical trial, two older individuals contracted Guillain-Barré syndrome.

This was enough for the FDA to flag the disease as “an important potential risk” from the RSV shot. Yet Pfizer is still seeking approval for general public use.

According to the Mayo Clinic, Guillain-Barré syndrome is a rare disorder in which your body’s immune system attacks your nerves.

While most people recover from Guillain-Barre syndrome, some severe cases can be fatal. Other serious cases can result in paralysis.

There’s no known cure for Guillain-Barre syndrome.

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Secret Pfizer Documents & New Studies prove COVID ‘Vaccine Shedding’ is occurring with deadly consequences

A study conducted by scientists at the University of Colorado confirms the vast majority of humanity has had absolutely no choice in the matter of whether they wish to get the Covid-19 injection or not because the vaccinated have been transmitting antibodies generated by the injections through aerosols.

The findings should however come as no surprise because a confidential Pfizer document had already confirmed exposure to the mRNA injections was perfectly possible by skin-to-skin contact and breathing the same air as someone who had been given the Covid-19 jab.

They also, unfortunately, add weight to the claims made by Dr Phillipe van Welbergen, who demonstrated that graphene, an alleged undisclosed ingredient of the Covid-19 injections, is being transmitted from the vaccinated to the not-vaccinated and destroying red blood cells and causing dangerous blood clots.

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Startling Evidence Suggests BioNTech and Pfizer Falsified Key Data

Evidence has emerged casting serious doubt over the authenticity of tests carried out by BioNTech (Marketing Authorisation Holder) and Pfizer to prove the fidelity of their product by demonstrating that only the spike protein of SARS-CoV-2 is expressed in cells by the nucleoside-modified mRNA Pfizer-BioNTech Covid-19 vaccine (BNT162b2).

Several Western Blot tests were conducted to evaluate the protein expression of the mRNA in HEK cells transfected with the vaccine taken from different lots. Using this technique, the expressed proteins showed up as highly unusual looking ‘bands.’

Certain independent scientific experts have described these Western blots as the “smoking gun” evidence (particularly the “duplication” of the results) which suggest that BioNTech and Pfizer falsified key data as part of their submissions to the European Medicines Agency and the US Food and Drug Administration  for securing emergency use authorisation (conditional) and later marketing authorisation approval of their product.

The bombshell evidence was dropped without so much as a ripple in the sea of brewing scandals washing up on the shores of the behemoth pharmaceutical company and its partner, BioNTech. However, some in the scientific community have taken notice and written about this scandal, known on social media as #Blotgate.

The fact there could be actual evidence to prove that Pfizer and BioNTech engaged in fraud by fabricating critical data would have major ramifications. For instance, their indemnity status (protection from any legal liability resulting from deaths or injuries caused by their product) which was written into their purchasing contracts and signed by many countries, would cease to apply.

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