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Pfizer Settles Over 10,000 Cancer Lawsuits

In a development that has largely flown under the radar, pharmaceutical giant Pfizer has quietly agreed to settle over 10,000 lawsuits tied to cancer risks associated with the popular antacid Zantac, according to federal prosecutors.

The lawsuits alleged that Pfizer concealed the cancer risks posed by Zantac, a widely used heartburn medication. The settlements cover cases filed across state courts in the United States, although the financial details of the agreements have not been disclosed to the public.

While the settlements mark a significant step in resolving the litigation surrounding Zantac, they do not entirely absolve Pfizer of its exposure to claims related to the drug. The news of the settlements is likely to provide some relief to investors, as concerns about the potential financial liabilities stemming from Zantac lawsuits had previously impacted the company’s market value.

Pfizer’s decision to settle comes amidst ongoing scrutiny over the safety and transparency of pharmaceutical products. Critics argue that the case highlights broader issues within the pharmaceutical industry, including allegations of deceptive marketing practices and suppression of critical information regarding product safety.

The controversy surrounding Zantac adds to the growing list of concerns surrounding Pfizer and other pharmaceutical companies, particularly in light of the COVID-19 pandemic. While Pfizer has emphasized that it ceased the production of Zantac more than 15 years ago, questions remain about the company’s handling of the drug and its potential health risks.

Despite the settlement, the fallout from the Zantac litigation underscores broader concerns about the pharmaceutical industry’s accountability and the need for increased transparency in drug safety regulation.

Concerning Link Between COVID Vaccination and Cancer Growth in the Wake of Pfizer’s $43 Billion Oncology Co. Acquisition

In a recent development that has sparked intrigue and concern, Pfizer completed a staggering $43 billion acquisition of Seagen on December 14, 2023, solidifying its position as the largest oncology company purportedly equipped to address cancers caused by mRNA vaccines. There’s an apparent link between COVID-19 vaccinations, specifically those utilizing mRNA technology, and an alarming surge in aggressive cancers, prompting serious safety concerns. The acquisition of Seagen is a move that positions the pharmaceutical giant as the largest player in the oncology market.

Pfizer’s acquisition of Seagen has raised eyebrows not only for its colossal price tag but also for the decision to issue $31 billion in debt to facilitate the purchase. Questions are circulating as to why Pfizer, a pharmaceutical giant with substantial resources, would opt for such a debt-heavy approach and overpay for a small cancer drug company that reports annual revenues of just $2 billion.

Pfizer’s COVID-19 mRNA vaccines, along with Moderna’s, are linked to the development of numerous forms of cancer. Researcher Dr. William Maki’s tweet states that cancers including lymphoma, brain cancer, breast cancer, colon cancer, and lung cancer are drastically increasing. Specifically, the CEO of Pfizer claims 33% of people are bound to develop cancer:

– 33% of people WILL get cancer (he’s certain)
– entire families WILL be affected (he’s certain)
– The new cancer treatments are like “missiles” that will target “most” cancers
– he will produce them AT A SCALE THAT HAS NOT BEEN SEEN BEFORE.
– 2025
– “We have a Global Network”
– “We have very quick way of completing clinical trials”
– will be produced “AT SCALE”, “just like mRNA”

The dramatic rise in cancer, especially among young adults, raises serious concerns about potential side effects from the COVID-19 vaccination. But equally troubling, why would one of the world’s largest manufacturers of the COVID vaccine pay a premium for the largest oncology company in the world? What does Pfizer know about the COVID vaccine’s link to surging cancer rates and when did it know it?
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Texas Attorney General Sues Pfizer for COVID Vax Lies

Eight months ago, Texas Attorney General Ken Paxton announced he was investigating Pfizer, Moderna, and Johnson & Johnson for potentially lying to the public concerning the success of their respective COVID-19 vaccines. . .

Paxton’s lawsuit alleges that Pfizer violated the Texas Deceptive Trade Practices Act, claiming that Pfizer “engaged in false, deceptive, and misleading acts and practices by making unsupported claims.”

Three weeks after Paxton had initially announced the investigation, he was impeached.

“The first thing I did when I came back was I told my staff, ‘I want to get back on this,’ and we did,” Paxton tells Sara Gonzales. . .

“Pfizer’s widespread representation that its vaccine possessed 95% efficacy against infection was highly misleading from day one,” the petition created by Paxton and his staff reads. (Read more from “Texas Attorney General Sues Pfizer for COVID Vax Lies” HERE)

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Pfizer Failed To Disclose Risks Of Preterm Birth And Neonatal Death To Pregnant Women In RSV Vaccine Trial

Pfizer failed to inform pregnant women participating in its clinical trial for the respiratory syncytial virus (RSV) vaccine that the clinical trial of a similar vaccine by GlaxoSmithKline (GSK) was halted after a safety signal revealed a potential risk of preterm births leading to neonatal deaths.

Even though Pfizer knew about the potential safety signal and was studying preterm births as an “adverse event of special interest,” it continued to enroll women in its clinical trial and did not fully inform participants of the risks the vaccine may pose to their babies—and in some cases, provided misleading and contradictory statements, according to an investigation by The BMJ.

“The BMJ article demonstrates Pfizer’s continued disregard for the law and patient choice,” attorney Thomas Renz told The Epoch Times in an email. “The entire point of informed consent is to ensure a patient can make a decision based on all available information. Rather than embracing the Nuremberg Code and American laws and regulations, Pfizer seems to view informed consent as a barrier to sales—something that causes vaccine hesitancy or drug hesitancy.”

“There should have never been a clinical trial in pregnant women studying any injections aimed at RSV in pregnant women,” Sasha Latypova told The Epoch Times in an email. “Pregnancy and potential to become pregnant is historically the most protected class of human subjects from clinical research because the risks and potential to cause inadvertent harm are too devastating to justify scientific interest in made-up subjects like RSV.” (Read more from “Pfizer Failed To Disclose Risks Of Preterm Birth And Neonatal Death To Pregnant Women In RSV Vaccine Trial” HERE)

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‘Feels Like Genesis 19’: Anti-Vaxxers Praise God for Tornado That Wrecked Pfizer Manufacturing Plant

Anti-vaccine conspiracy theorists are claiming God sent a tornado to North Carolina on Wednesday to severely damage a Pfizer manufacturing plant.

Located in the city of Rocky Mount, the 250-acre site, which produces a significant portion of the country’s sterile injectables, was crushed by winds reaching upwards of 150mph when a twister passed through the area.

The plant, which also manufactures vials, IV bags, and bottles of anesthesia, saw more than 50,000 pallets of goods strewn across the site. No one at the plant received any serious injuries as a result. . .

A writer for the conservative outlet the Blaze, for example, used the incident to state that God clearly had a “sense of humor.” Another user argued that the tornado had actually saved lives by damaging the plant.

(Read more from “‘Feels Like Genesis 19’: Anti-Vaxxers Praise God for Tornado That Wrecked Pfizer Manufacturing Plant” HERE)

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Former Pfizer Employee Charged With Insider Trading Related to COVID Treatment

A former employee for Pfizer was charged by federal investigators on Thursday after being accused of insider trading related to non-public results related to COVID drug Paxlovid.

Amit Dagar, 44, was charged with four counts of securities fraud and one count of conspiracy to commit securities fraud after federal investigators said that he used his knowledge of Paxlovid trials to purchase stock in Pfizer ahead of the release of positive test results.

Dagar “purchased short-dated, out-of-the-money call options in Pfizer stock. DAGAR also tipped his close friend, ATUL BHIWAPURKAR, about the coming drug results and BHIWAPURKAR also purchased short-dated, out-of-the-money Pfizer call options that expired approximately two weeks later. BHIWAPURKAR also tipped another friend (‘Individual-1’), who similarly purchased short-dated, out-of-the-money Pfizer call options that expired approximately three weeks later,” the Southern District of New York’s Department of Justice’s office said.

Bhiwapurkar, from California, was also charged with two counts of security fraud and one count of conspiracy to commit security fraud. The two are accused of purchasing the stocks in November 2021 after Dagar saw positive results from the company’s testing of Paxlovid ahead of their public release. (Read more from “Former Pfizer Employee Charged With Insider Trading Related to COVID Treatment” HERE)

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Big Pharma Funds Activist Group’s Effort To Push Trans Ideology On US Hospitals: REPORT

Pfizer and PhRMA, a pharmaceutical trade association, funded a medical index that pushes LGBTQ ideologies on young patients while penalizing American hospitals that refuse to follow the index criteria, according to The Washington Free Beacon.

The Human Rights Campaign (HRC) introduced the Healthcare Equality Index (HEI) in 2022, a scorecard that surveys U.S. hospitals “dedicated to the equitable treatment and inclusion of their LGBTQ+ patients, visitors, and employees” according to The Washington Free Beacon. PhRMA and Pfizer fund the index that rates hospitals based on their compliance with its criteria.

According to the HEI, hospitals that want to attain a perfect score must exhibit LGBTQ symbols, use patients’ preferred pronouns and administer LGBTQ training programs approved by the HRC, according to the scoring criteria.

The HRC criteria pressures doctors to provide treatments to patients who claim to be transgender without showing symptoms of gender dysphoria while punishing medical institutions that oppose this medical procedure. The index also deducts 25 points from medical facilities for conduct deemed discriminatory against the LGBTQ community and for refusing to perform a hysterectomy or mastectomy on young patients. (Read more from “Big Pharma Funds Activist Group’s Effort To Push Trans Ideology On US Hospitals: REPORT” HERE)

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German Press Discusses Pfizer Vaccine Trial Fraud. Will “COVID Reckoning” Follow?

I am pleasantly surprised to see the mainstream German publication Die Welt openly asserting that clinical trials of the “Pfizer COVID vaccine” were rife with fraud. (paywall-free German language link, PDF with English translation) What a change! . . .

The article explains that Pfizer unblinded and removed numerous patients who suffered adverse events from the Covid vaccine trial. It also gives examples of Pfizer subjects whose deaths were covered up. One of the victims described by Die Welt is Pfizer subject C4591001 1162 11621327, whose story I unearthed in July of 2022.

WELT has documents according to which patient no. 11621327 was found dead in his apartment three days after the 2nd dose, apparently a stroke. Patient #11521497 died 20 days after vaccination, diagnosis of cardiac arrest. “According to the current state of science, these two cases would be assigned to the vaccination,” says the Berlin pharmaceutical specialist Susanne Wagner, “especially since the US health authority CDC is currently investigating strokes in vaccinated people and it is known

As you remember, Pfizer’s investigators falsely ruled these deaths unrelated.

Die Welt also describes Argentine lawyer Augusto Roux, who remained alive, but whose sufferings were written off as “anxiety.”

Three weeks later, test candidate Roux received the second dose. He remained under observation for 40 minutes, then left the hospital feeling good. In the taxi home he felt uncomfortable, and later he had shortness of breath, burning chest pain, nausea and fever. His urine turned black like cola and he passed out. Three days later, Roux was in the Alemán Hospital, several PCR tests for Covid were negative. Senior physician Gisela di Stilio noted in the discharge report, which is available to WELT: “Adverse reaction to the coronavirus vaccine (high probability)”. The computer tomograph had provided images of fluid in Roux’s heart. A pericardial effusion.

Over the next few months, Roux lost 14 kilos, he had liver problems, and his heart sometimes beat irregularly. … The diagnosis for the symptoms after the second vaccination is very likely to be “pericarditis”, inflammation of the heart. All of this fits exactly with a clinical picture that the Paul Ehrlich Institute also has in its list of “rare side effects” for mRNA vaccines.

Note how Die Welt sarcastically puts “rare side events” in quotes.

… He found amazing things there. His story, one might think, should appear in Pfizer’s pivotal study papers, but it doesn’t. The pharmaceutical company’s papers say Roux informed the research team that he was hospitalized with pneumonia on both sides, following the initial report, which was classified as an “adverse event of toxicity level 1”. That could have nothing to do with the vaccine, the file goes on to say, it is probably a Covid infection. Not a word that Roux had tested negative for Corona in several PCR tests.

The paper finds more cases of Pfizer fraud:

Almost at the same time as the Roux case, there must have been an incident in the Buenos Aires test center. In one fell swoop, the test management said goodbye to 53 subjects on August 31, 2020. The test candidates were “unblinded”, which means they were informed about their vaccination status, a process that the Pfizer study protocol expressly only provides for “in emergencies”. But there is nothing about it in the approval study. In protocol documents that are available to WELT, and which are actually not intended for the public, those responsible get caught up in contradictions.

(Read more from “German Press Discusses Pfizer Vaccine Trial Fraud. Will “COVID Reckoning” Follow?” HERE)

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COVID Vax May Affect Female Fertility, Pfizer Official Admits in New Project Veritas Sting

Project Veritas released a video Thursday allegedly showing a Pfizer executive expressing concern about his company’s mRNA vaccines and their impact on female reproductive health.

Jordon Trishton Walker, Pfizer’s director of research and development, strategic operations – mRNA scientific planner, recently appeared to tell an undercover Project Veritas journalist that the company has considered using “directed evolution” to mutate coronaviruses and create more potent variants and vaccines. More footage captured by the journalist allegedly shows the executive revealing that Pfizer is not entirely sure why the vaccine is impacting women’s menstrual cycles, postulating that the effects could be evidence of hormonal disruptions.

“There is something irregular about their menstrual cycles. So, people will have to investigate that down the line, because that is a little concerning. The vaccine shouldn’t be interfering with that,” he said. “There’s something happening, but we don’t always figure it out.”

“I hope we don’t find out that somehow this mRNA lingers in the body,” he continued,” because it has to be affecting something hormonal to impact menstrual cycles.”

(Read more from “COVID Vax May Affect Female Fertility, Pfizer Official Admits in New Project Veritas Sting” HERE)

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Pfizer Plans To Profit From COVID For Years To Come

Pfizer has already profited billions of dollars from the COVID-19 pandemic, and it plans to do so for years to come via annual vaccinations and sales of its antiviral pill Paxlovid.

The company doubled its revenue from 2020 to 2021, bringing in more than $81 billion, and also gained a large foothold in the American regulatory process, according to Kaiser Health News. CEO Albert Bourla and other top executives have said they plan to continue taking advantage of the COVID-19 market for the foreseeable future.

“Hopefully, we could be giving it annually and maybe for some groups that are high-risk more often,” Bourla told investors earlier this year, referring to COVID-19 booster shots and vaccines tailored to specific variants. “Then you have the treatment [Paxlovid] that will, let’s say, resolve the issues of those that are getting the disease.”

Some patients have experienced issues with “rebound” infections with Paxlovid, cases where they begin experiencing stronger symptoms again after completing their series of the antiviral pill. That won’t stop Pfizer from selling millions more doses though, executives said.

“People are going to get out there,” the president of Pfizer Biopharmaceuticals Group, Angela Hwang, said in May. “We know with all of that, infections are going to increase, and that’s the role that Paxlovid can play.”

(Read more from “Pfizer Plans To Profit From COVID For Years To Come” HERE)

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