Endotoxin in Pfizer Jabs causes Huge Range of Diseases with upregulation of IL-15, IFN-γ and IP10/CXCL10 among other things

The paper I discuss is from the Greek Clinical Trial NCT04743388 studying the Cytokine Storm in Pfizer Jabbees after their 1st and 2nd Jabs.12

I had this paper brought to my attention by Walter Chesnut in his recent article where his focus is on the Inflammatory effects of the GMO Spike Protein and mine will predictably be on the effects of the Endotoxin that is known to be present in every Lot as the completely uncontrolled preferred “adjuvant” obtained free from the toxic E. coli soup of Process 2 poojabs.34

Here is the Figure from the Greek Pfizer Trial paper.5

Notice the primary Target Lymph Nodes.

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DNA Contamination in Pfizer COVID Shot 500 Times Permissible Level: New Study

Genetic impurities in the Pfizer mRNA COVID vaccine could be as high as 500 times the permissible limit, according to a new study.

In the study, published in Methods and Protocols, two German researchers raise worrying questions about the reliability of the quantitative PCR technique used by Pfizer-BioNTech to measure DNA contamination in the vaccine.

Using their own tests on the vaccine’s lipid nanoparticles, they discovered levels that were between 360 and 534 times higher than the 10 nanogram per dose limit set by regulators.

The researchers argued that the methods used by Pfizer-BioNTech test for only 1% of the original DNA template used to make the vaccine, meaning that 99% of the genetical material from the template therefore goes untested and potentially undetected.

Similar concerns have been raised by other researchers.

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Pfizer’s Covid Gene Therapy Shots Have Over 500 Times Allowable Levels of DNA Contamination — Study

study published this month has found that the Pfizer mRNA Covid ‘vaccine’ gene therapy injections contain DNA contamination at over 500 times allowable levels, raising fears that the DNA may integrate into the vaccinated person’s own DNA, causing mutations that can lead to diseases such as cancer.

“The available information and data indicate that the ready-to-use mRNA vaccine Comirnaty contains DNA impurities that exceed the permitted limit value by several hundred times and, in some cases, even more than 500 times,” the study said in the ‘Conclusions’ section.

Modified messenger RNA (mRNA) vaccines work by encapsulating the RNA sequence of the Covid spike protein (the dangerous part of Covid, linked to HIV) into lipid nanoparticles which are able to deliver the RNA payload into the body’s cells. The RNA is then integrated into the person’s genetics so they will produce the Covid spike protein, which the body can then develop an immune response to.

However, according to the study, mRNA is not the only genetic information being injected into people.

“…in addition to the mRNA active ingredient, DNA impurities are also encased in lipid nanoparticles and are therefore difficult to quantify,” the study said in the ‘Abstract’ section.

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Whistleblower Exposes Internal Email Suggesting Pfizer Offered “Separate and Distinct” COVID-19 Vaccines to Employees

A whistleblower from Pfizer has leaked an internal email indicating that the pharmaceutical giant offered a “separate and distinct” COVID-19 vaccine to employees at its Pearl River research site in Rockland County, New York, InfoWars reported.

The email, dated January 2021, reassures  Pfizer employees that the vaccine supply for this internal program would not affect the doses committed to national governments worldwide.

According to the leaked document, site-essential workers were identified to receive these exclusive vaccinations.

According to the whistleblower, there was a widespread belief among employees that they were receiving vaccines that were different from those distributed to the public.

“I know we employees at Pfizer were receiving different vaccines and/or placebos, and this was the word around my site when I worked there,” the whistleblower told Infowars.

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Pfizer To Bypass Doctors, Pharmacies By Selling Drugs Online Directly To Consumers: Report

Pfizer is forging ahead with plans to introduce a direct-to-consumer platform for online sales of some of its medications, including Paxlovid and a migraine nasal spray.

The Defender reports that this initiative marks the latest maneuver by major pharmaceutical companies to circumvent conventional routes of distribution through primary care physicians and brick-and-mortar pharmacies. 

Pfizer is set to roll out its platform before the year’s end. 

Its website will enable patients in the U.S. to consult independent telehealth professionals for prescriptions, with an online pharmacy partner handling the fulfillment and shipping of orders, per the Financial Times.

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Toddler Dies in Pfizer Gene Therapy Trial

Yesterday I republished a video and article entitled, “What Happened to Their Babies,” describing the lack of ethics and grossly inhumane experimentation that Pfizer conducted on babies and toddlers with their COVID-19 mRNA gene-editing injections.

Just a few hours ago, multiple industry outlets began breaking this official statement from Pfizer that a toddler died of a cardiac arrest in an investigational trial of boys, aged 2 to 4 year olds, to treat a rare form of muscular dystrophy with a recombinant adenovirus gene editing technology.

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Pfizer agrees to settle 10,000 lawsuits accusing pharma giant of hiding cancer risks of heartburn drug Zantac

Pfizer has agreed to settle more than 10,000 lawsuits alleging it it of hiding the cancer risks of its heartburn drug Zantac.

The financial details have not been revealed but pharma rival Sanofi agreed to pay more than $100million to resolve 4,000 Zantac-cancer claims last nonth.

The over-the-counter pill was pulled in the US in 2020 after animal studies found a key ingredient released ‘probable human carcinogens’.

Pfizer was the primary manufacturer of Zantac from 1998 to 2006, when several suits claim it should have known that the drug was contaminated with NDMA.

Plaintiffs claimed the drug was contaminated with the impurity through improper manufacturing practices, and that Pfizer withheld this information from consumers.

NDMA is a chemical byproduct of many industrial manufacturing processes, including the production of rocket fuel.

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CDC Concealed Evidence Linking Deaths to Pfizer and Moderna COVID-19 Vaccines, Internal Documents Reveal

U.S. Centers for Disease Control and Prevention (CDC) officials found evidence that the Pfizer-BioNTech and Moderna COVID-19 vaccines caused multiple deaths before claiming that there was no evidence linking the vaccines to any deaths.

The US public health regime and the bootlicking media have been routinely downplaying the risk of developing myocarditis after taking the vaccine, calling the occurrence “mild” and “rare,” and systematically burying any evidence to the contrary.

According to the documents obtained by The Epoch Times, CDC employees conducted investigations into reported post-vaccination deaths, particularly focusing on cases involving myocarditis, a known side effect of the Pfizer-BioNTech and Moderna COVID-19 vaccines.

Their findings, spanning the end of 2021, highlighted instances where myocarditis was listed on death certificates and in autopsies for some individuals who had received the vaccines. In some cases, myocarditis was even attributed directly to vaccination.

The file also showed instances where deaths met the CDC’s definition for myocarditis, with symptoms appearing within 42 days of vaccination and no virus-related symptoms present.

Despite these findings, the CDC maintained that it had seen no signs linking the Moderna and Pfizer mRNA vaccines to any deaths reported to the Vaccine Adverse Event Reporting System (VAERS).

The VAERS database contains information on unverified reports of adverse events (illnesses, health problems and/or symptoms) following immunization with US-licensed vaccines.  The CDC government website links to the VAERS platform.

What VAERS Says: “‘VAERS occasionally receives case reports from US manufacturers that were reported to their foreign subsidiaries. Under FDA regulations, if a manufacturer is notified of a foreign case report that describes an event that is both serious and unexpected (in other words, it does not appear in the product labeling), they are required to submit it to VAERS.”

Dr. Clare Craig, a British pathologist, and Dr. Andrew Bostom, a heart expert, both expressed concerns about the CDC’s stance. Dr. Craig told The Epoch Times that it was “absolutely” safe to say that the vaccines caused the deaths in cases where myocarditis was listed as the cause and met the CDC’s definition.

Dr. Bostom accused the CDC of “concealing these deaths” and “putting out a dishonest line” by claiming there were no deaths related to the mRNA vaccines.

A CDC spokeswoman declined to explain why the agency doesn’t consider autopsies or death certificates as evidence of causality and did not address questions about specific deaths outlined in the file, citing privacy concerns.

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New Studies: Pfizer’s Paxlovid doesn’t actually work, ‘rebound’ symptoms occur 25x more often than advertised

I wanted to turn your attention to two significant recent studies on Paxlovid, the Covid-19 oral pill that the U.S. government spent $12.6 billion taxpayer dollars on subsidizing for Pfizer.

The first study, which is brought to you by Pfizer funds (though they noticeably don’t use the brand name Paxlovid in the study), finds that Paxlovid does not actually work. They’ve known this since July, 2022, but for reasons unknown, waited two years to publish the results.

“The time to sustained alleviation of all signs and symptoms of Covid-19 did not differ significantly between participants who received nirmatrelvir–ritonavir (Paxlovid) and those who received placebo,” the authors write in this New England Journal of Medicine study, which was published on April 3rd.

That’s right. It doesn’t work at all.

In rolling out Paxlovid, Pfizer claimed in a press release that its preliminary data showed an 89% reduction in hospitalization and death for patients who took the pill.

Curiously, the Pfizer-funded study concluded in July 2022, just months after Paxlovid became available, but this seems to be the first time that results have been public.

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Pfizer Chemical Spill in Michigan Causes No Contact Advisory of Kalamazoo River

A no-contact advisory was issued for the Kalamazoo River after a chemical spill occurred at Pfizer’s manufacturing plant in Kalamazoo, Michigan.

According to city health officials, Pfizer released over 1,057 gallons of methylene chloride in its manufacturing facilities processing area, which was then discharged into the Kalamazoo River.

Methylene chloride is a colorless liquid that Pfizer and other pharmaceutical manufacturers use as a solvent in their pharmaceutical medicines.

After the chemical spill occurred, Kalamazoo County Health Officials warned residents not to come into contact with the Kalamazoo River.

Kalamazoo County Health Officer Jim Rutherford stated, “We decided to issue a no-contact advisory for the stretch of river impacted by the methylene chloride release as a precautionary measure.”

“This advisory will remain in effect until further investigation and sampling indicates that there is no risk to public health,” added Rutherford.

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