Pfizer purchased companies that produce drugs to treat the same conditions caused by covid vaccines

In 2017 a former vice president of Pfizer blew the whistle and said that pharmaceutical companies intentionally design vaccines to keep the public in a state of illness to profit from the treatments of vaccine-induced illnesses. 

Pfizer’s acquisitions of other pharmaceutical companies since the rollout of its covid vaccine seem to indicate this is indeed the case.

In 2021, Pfizer’s acquisition of Arena Pharmaceuticals raised eyebrows. The purchase price seemed disproportionate to the market size of the drug they acquired – a drug that is a potential therapy for all kinds of immuno-inflammatory diseases, including inflammation of the heart.  As we know, myocarditis began to skyrocket after the rollout of Pfizer’s mRNA vaccines.

In 2023, Pfizer purchased Seagen Pharmaceuticals, known for its cancer drugs.  Was this because of the connection between the mRNA injections and “turbo cancers”?

In 2022, Pfizer purchased Global Blood Therapeutics for its drug to treat sickle cell disease, again for an amount that seemed disproportionate to the profit the company could make off the drug considering how many people have the disease.  Does Pfizer know something we don’t? Will we see a blood cell disease epidemic as well?

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4 More U.S. States Sue Pfizer Over False COVID Vaccine Claims

Four additional states will follow Kansas’s lead by filing large-scale lawsuits against pharmaceutical giant Pfizer. These states allege that the company misled the public regarding the safety and efficacy of its COVID-19 vaccine.

Last week, Kansas Attorney General Kris Kobach announced that he is suing pharmaceutical giant Pfizer for misleading Kansas residents about the safety and efficacy of its COVID-19 vaccine.

During a press conference in Topeka, alongside Deputy Attorney General Fran Oleen and Assistant Attorneys General Kaley Schrader and Melanie Jack, Kobach detailed the allegations lodged against Pfizer.

“Kansas is filing a civil suit against the Pfizer Corporation under the Kansas Consumer Protection Act, seeking enhanced civil monetary penalties, damages, and injunctive relief for misleading and deceptive statements made in marketing its COVID-19 vaccine. Pfizer also violated previous consent judgments with the state of Kansas, in which Pfizer promised never to use deceptive information to market their products,” said Kobach.

The complaint, lodged today in Thomas County District Court, accuses Pfizer of misleading Kansans about the vaccines’ risks, including potential harm to pregnant women and the risk of myocarditis. The suit further alleges that Pfizer falsely claimed its vaccine was effective against COVID variants, despite evidence to the contrary.

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All Cause Mortality Higher in the Covid-Vaccinated — Study

study published Sunday detailed how individuals who received the Covid vaccine were more likely to die, while their booster dose did nothing to help them.

In order to view the full study one must download the PDF file.

“…those vaccinated with one or two doses who had significantly higher risks than the unvaccinated,” the study said in the ‘Conclusion’ section. “We found all-cause death risks to be even higher for those vaccinated with one and two doses compared to the unvaccinated and that the booster doses were ineffective. We also found a slight but statistically significant loss of life expectancy for those vaccinated with 2 or 3/4 doses.”

The researchers analyzed data from the Italian province of Pescara for their paper.

Interestingly, the researchers calculated the loss of life expectancy of those who were injected with the exotic gene therapy technology, or rather, how many days of life is lost on average per shot.

They used the ‘restricted mean survival time’ (RMST) and the ‘restricted mean time lost’ (RMTL) to articulate the data.

“…we calculated the RMST difference that represents the best index of “life expectancy” in those comparisons where the assumptions of the model were not met [12], and with the RMTL ratio that can approximate the HR in the absence of proportional hazard assumption [13]. The RMST difference represents the days of life lost by the vaccinated population compared to those of the unvaccinated one, while the RMTL ratio represents the percentage of life expectancy lost in the vaccinated population compared to in the unvaccinated one,” the study said in the ‘Discussion’ section. “The differences in RMSTs between the vaccinated and unvaccinated are significant for both the two-dose and the three-or-more-dose groups. They may appear irrelevant (in the order of a few days), but they refer to a limited period of time (739 days for those vaccinated with two doses and 579 days for those vaccinated with three or more doses). They could be compared with the entire life expectancy of an individual, which in the province of Pescara has an average value of 82.6 years [14] (corresponding to 30,149 days).”

Surprisingly, those vaccinated with two doses lost more time on this earth than those vaccinated with three or more doses, however that is likely due to the fact that those only vaccinated with two doses died before they had the opportunity to receive their third.

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Lawyer breaks media silence on Ottawa Detective’s probe into sudden infant death increase

An Ottawa police detective is facing trial for allegations of misconduct after investigating a series of unusual sudden infant deaths in the region, in 2021 and 2022.

Detective Helen Grus, who was working at the time for the sexual assault and child abuse unit (SACA) for the Ottawa Police Service (OPS), is accused of unauthorized access of an internal database while researching a potential link between the novel COVID-19 mRNA vaccines and an uptick in sudden infant deaths after their roll out.

During her tribunal defence hearing in May of this year, Grus presented evidence of a roughly 97% fatality rate among unborn babies in Pfizer’s clinical trial data. This full disclosure could not be heard because Grus was interrupted and silenced by the hearing officer, retired superintendent Chris Renwick, who has no legal training.

The defence suspects that the police and the hearing officer are politically motivated to silence and prosecute Grus, disregarding potential criminality around this alarming trend affecting the most vulnerable population.

Grus’ lawyer, Bath-Sheba van den Berg, describes the unsettling incident as unlike anything she has witnessed in proceedings before.

“She’s sitting there in front of me, facing me,” details van den Berg, “and she’s stating simply that, 31 out of 32 [babies died]. And as she was stating that, the hearing officer lurched forward and said ‘stop.’”

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1/200 chance of death in context of new bird flu injection – 5 times higher than placebo according to clinical trial

On June 26, 2024, Reuters wrote a piece announcing the looming threat of plans to offer preemptive bird flu injection to the people of Finland who work with animals.

It’s important that the people of the world understand something about the so-called AUDENZ™ (Influenza A (H5N1) Monovalent Vaccine, Adjuvanted), another product in clinical trials that will soon be offered to the public to fight ‘bird flu’.

Some details: It’s a 2-doser – 21 days apart. Anaphylaxis is counter-indicated and a precautionary warning pertaining to Guillain-Barré syndrome is listed in the prescribing information sheet.

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Stroke Risk: COVID Shots 200 Times More Likely to Cause Blood Clots in Brain

The COVID-19 vaccines carry a much higher risk of blood clots in the brain compared with other vaccines, according to a new study by Dr. Peter McCullough and colleagues.

The researchers looked at reports in the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS) from January 1990 through December 2023.

They counted the number of cerebral thromboembolism events — as in, blood clots of the brain’s veins or arteries — reported in people who received a COVID-19 shot compared with those who received a flu shot or other vaccines.

Blood clots that block blood flow to the brain account for roughly 87% of all strokes, according to the American Stroke Association, a division of the American Heart Association.

McCullough — a cardiologist with over 1,000 publications and over 685 citations in the National Library of Medicine — told The Defender the study showed “an unacceptable risk of catastrophic thrombotic injuries to the brain” in individuals who took one or more COVID-19 shots.

McCullough summarized the study’s results on Substack:

“Compared to influenza vaccines given over 34 years, COVID-19 vaccines in 36 months of use had over 1000-fold increased risk of most blood clot events, and compared to all vaccines combined administered over 34 years, this risk remained at over 200-times greater with COVID-19 vaccination.”

Prior research has suggested that the spike protein in both the SARS-CoV-2 virus and the COVID-19 vaccine can cause serious blood clotting, McCullough and his co-authors noted in their report.

Blood clots in the brain are difficult to treat, McCullough told The Defender, and “oftentimes leave patients with devastating disabilities.”

“This and other sources of data,” he added, “support calls to remove all COVID-19 vaccines from public use.”

The study — co-authored with Claire Rogers, Dr. James Thorp and Kirstin Cosgrove — is under peer review and available online as a preprint.

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Vaccines in the Food Supply: What Are the Risks?

In my previous articles, we looked at the global war on farmers, the organizations pushing for the Great Food Reset, the tactics used to foist these changes on the public, and the projects underway to remove your access to healthy, farm-fresh foods.

Today we will delve into the contentious issue of vaccines in the food supply. Accurate information on this topic is not easy to find.

The U.S. Department of Agriculture (USDA) and drug developers aren’t required to release any information on veterinary drugs in the development pipeline, so independent detectives are left searching through peer-reviewed papers, university publications, USDA contracts, grant notifications, company white papers and university websites to learn what is on the horizon.

This system is far from transparent, and frankly, I don’t think that’s an accident.

Before any vaccine technology is used on humans, it is usually tried in the veterinary market first due to the incredibly lax regulations. Knowing this, it should come as no surprise that our food animals had been receiving mRNA injections for years before the COVID-19 vaccine rollout.

Around 2014, the USDA granted a conditional license for an mRNA vaccine for use in pigs for the Porcine Epidemic Diarrhea Virus. This is equivalent to emergency use authorization and gets around the USDA’s vaccine licensing and authorization process.

In 2015, Merck bought Harrisvaccines to acquire their RNA platform. Merck’s 2015 press release stated that this “RNA Particle technology … represents a breakthrough in vaccine development.

It also has a highly versatile production platform able to target a wide range of viruses and bacteria.

Pathogens are collected from a farm, and specific genes are sequenced and inserted into RNA particles, making safe, potent vaccines able to provide herd-specific protection.”

Introduced in 2018, Sequivity is Merck’s RNA vaccine platform built on the Harrisvaccines technology. These RNA injections are already in use in pigs.

They are customized for different viruses, and each customized injection undergoes no new safety testing; new formulations are deployed immediately. The pork you are eating from the supermarket is already likely treated with these gene therapies.

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Guillain-Barré Syndrome ‘More Common Than Expected’ in Early RSV Vaccine Trial

Reports of the nervous system disorder Guillain-Barré syndrome (GBS) were “more common than expected” in the older adult population who received the new vaccine for respiratory syncytial virus (RSV). The data, reported by the U.S. Centers for Disease Control and Prevention (CDC), matched trial data reported earlier this year.1

GBS is a “polio-like” inflammatory autoimmune disorder in which a person’s immune system damages nerve cells, which can result in muscle weakness and paralysis of the face, respiratory system and limbs, including full body paralysis and can lead to death. GBS usually develops after an infection and symptoms include numbness and tingling, throbbing pain, heart rhythm problems, high blood pressure, slurred speech, difficulty swallowing and shortness of breath. Most people recover but, in some cases, the nerve damage is permanent.2

Current recommendations state that patients over the age of 60 should talk to their doctor to decide whether they should get the new RSV vaccine. Government officials still say that the benefits of the vaccine outweigh the risks and that they do not plan to change their recommendations.1

The most recent CDC report highlighted 28 cases of RSV vaccine-related GBS and all but one developed symptoms of GBS within 21 days after being vaccinated. Data from the Vaccine Adverse Event Reporting System (VAERS) revealed that there were 1.5 cases per one million in people who received GlaxoSmithKline’s (GSK) Arexvy RSV vaccine, and five cases per one million in people who received Pfizer’s Abrysvo RSV vaccine.

There were 18 reported deaths after RSV vaccinations that were attributed to “a variety of reasons,” two of which were associated with GBS. Other reported causes of death included severe respiratory illness and failure, cardiovascular events, hepatic encephalopathy, RSV infection, and sepsis, among others.3

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Lawsuit On Behalf Of Vaccine-injured Seeks To Strike Down ‘Unconstitutional’ PREP Act

lawsuit filed Tuesday seeks to strike down the PREP Act — the federal law that granted legal immunity to companies such as Pfizer and Moderna for injuries caused by their COVID-19 vaccines and other COVID-19 countermeasures.

The lawsuit, filed in the U.S. District Court for the Middle District of Florida, Tampa Division, alleges the Public Readiness and Emergency Preparedness (PREP) Act violates the U.S. Constitution and the Administrative Procedure Act, which governs how federal agencies develop and issue regulations.

Plaintiffs in the suit include the nonprofit Moms for America and individual plaintiffs who were injured by a COVID-19 vaccine, or whose loved one suffered injury or death from a COVID-19 vaccine.

According to the complaint, “This case is about the government’s failure to resolve conflicts involving Americans killed or grievously harmed while receiving healthcare during the COVID-19 pandemic.”

Defendants are the U.S. Department of Health and Human Services (HHS), the U.S. Health Resources and Services Administration, HHS Secretary Xavier Becerra and President Joe Biden.

“As even The New York Times has recently acknowledged,” Jeff Childers, attorney for the plaintiffs, told The Defender, “too many Americans have been injured by the COVID vaccines and other rushed treatments, and now have no recourse, no help and no support. They can’t sue anybody, thanks to PREP.”

“PREP was poorly conceived, badly executed, and gave far too much power to unelected bureaucrats and executive agencies,” he added.

Childers wrote on Substack today that the PREP Act should “be crushed and burned to a cinder in the incinerator of history’s worst ideas.”

The lawsuit asks the court to declare the PREP Act unconstitutional and to declare that the HHS secretary’s actions in implementing the act violate the Administrative Procedure Act.

The suit also asks the court to declare that the plaintiffs can sue companies like Pfizer and Moderna in federal and state courts. It also seeks compensation for attorney fees.

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Study Finds Alarming Surge In Deaths From Neurological Disease Among Young Adults

A recent preprint study which relies on extensive data from the Centers for Disease Control and Prevention (CDC) paints a concerning picture of the neurological health landscape in the United States. The study, which focuses on those aged 15-44, reveals a disturbing increase in deaths from neurological diseases both as the primary cause and among multiple contributing factors.

This uptick in mortality rates, which is particularly significant among younger adults, could have profound implications for the nation’s public health policies, especially in the wake of the COVID-19 pandemic.

Perhaps most concerning, the study found an increase in neurological complications following COVID-19 vaccinations, including conditions such as Guillain-Barré syndrome and acute disseminated encephalomyelitis.

According to Phinance principal Ed Dowd, “The results show a clear break from the prior historical trend in death rates from neurological diseases.”

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