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Showing posts with label Unsafe-Ineffective. Show all posts
Showing posts with label Unsafe-Ineffective. Show all posts

Friday, October 2, 2026

Florida AG Sues Pfizer Over mRNA Deception

An Intro by John R. Houk, Blog Editor

Intro © October 2, 2026

 


I’ve read Florida Attorney General James Uthmeier is conducting a civil suit against Pfizer and its CEO Albert Bourla for knowingly misrepresenting the safety and effectiveness of its mRNA Jab during the COVID Tyranny.

 

I say, “GO FLORIDA!”

 

And yet I have a suspicion Big Pharma – including Pfizer – will rally their corrupt politicians and a corrupt Federal Judiciary to quash the sovereign State of Florida (as AGAIN ignoring the 10th Amendment) in the State’s ability to protect Florida citizens.

 

On the other hand, perhaps an ultimate legal SCOTUS miracle will arise affirming Florida’s 10th Amendment sovereign rights and Pfizer gets spanked in State Court. Just think of the slew of Red-State Courts taking the precedent to sovereignly protect their State citizens from the heinous greed of Big Pharma. I suspect this is litigation that eventually land on the SCOTUS Docket probably after the Trump Administration ends its term of Office.

 

I’m cross post the Florida lawsuit details from The Exposé and Substack’s FOCAL POINTS. But for a brief synopsis take a look at Bob Unruh’s post at WND: “'Deceptively marketing the products as safe': Pfizer sued for deceiving public about COVID shots: Allegations from state attorney general are that company profited while refusing to disclose serious risks”.

 

JRH 10/2/26

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Florida Attorney General files lawsuit against Pfizer for deceptive practices relating to its covid “vaccine”

Featured image: Florida Attorney General James Uthmeier announcing lawsuit against Pfizer and its CEO. (The Exposé PHOTO)

 

Posted by Rhoda Wilson

October 2, 2026

THE EXPOSÉ

 

Yesterday, 1 October 2026, Florida Attorney General James Uthmeier filed a lawsuit against Pfizer and its CEO Albert Bourla, alleging the company violated Florida’s Deceptive and Unfair Trade Practices Act.

 

The complaint claims Pfizer deceptively marketed its covid vaccine as safe while concealing known risks, including myocarditis and dangers to pregnant women.

 

“Weeks ago, we learned Fauci and the biomedical state knew the covid jabs were dangerous but hid it from us. While that investigation continues, today we sued Pfizer for deceptively marketing the products as safe- making billions -while pregnant women were miscarrying their babies and teenagers were having heart attacks,” Uthmeier said in a tweet.

 

Pfizer’s Vaccine Messaging Heads to Court in Florida

By RVM News

 

Florida Attorney General James Uthmeier announced a lawsuit against Pfizer and CEO Albert Bourla, accusing the company of deceptive practices involving the marketing and safety claims surrounding its mRNA covid-19 vaccine.

 

Uthmeier said Pfizer presented mass vaccination as necessary to stop the spread of covid-19 while assuring the public that there were no significant safety concerns.  “Pfizer told Florida families that mass vaccination with their mRNA covid vaccine was necessary to stop the spread, and that there were no material safety risks,” Uthmeier said.

 

He specifically pointed to comments from Bourla that, according to Uthmeier, pressured people to take the vaccine by suggesting they would otherwise endanger those closest to them.  “CEO Albert Bourla said, ‘If you didn’t take it, you were putting the people you love the most at risk. He called people who asked questions criminals,” Uthmeier said.

 

The attorney general also criticised Pfizer’s public statements about potential safety concerns following the widespread distribution of the vaccine. “In January 2023, after billions of doses, he said Pfizer had not seen a single safety signal,” Uthmeier said.

 

Uthmeier argued that Pfizer had enormous financial incentives surrounding the vaccine and spent heavily on advertising while generating tens of billions of dollars from sales.  “They spent 10 billion dollars on advertising. They brought in more than 80 billion from the vaccine alone,” Uthmeier said.

 

At the centre of Florida’s allegations is Uthmeier’s claim that the company failed to adequately disclose information about potential risks.  “What they didn’t say was that they knew about myocarditis in teenagers and young adults,” Uthmeier said.

 

He further claimed that Pfizer had received thousands of reports involving adverse events.  “They had reports of 1,000s of adverse events, including stroke and death, and they had reason to know the shot posed risks to pregnant women and unborn babies in the first trimester,” Uthmeier said.

 

Uthmeier also referenced information he said was recently revealed by Senators Rand Paul and Ron Johnson involving Dr. Anthony Fauci and concerns about pregnancy.  “Recently, Senators Paul and Johnson revealed that Dr. Anthony Fauci texted that the second dose theoretically could be associated with miscarriage in the first trimester,” Uthmeier said.

 

According to Uthmeier, other federal health officials were aware of the discussion while pregnant women continued to be told that vaccination was safe.  “The CDC director and the Surgeon General agreed, but pregnant women, nevertheless, were told it was safe,” Uthmeier said.

 

The Florida attorney general also alleged that Pfizer had not established whether the vaccine prevented transmission before making claims about the broader public-health benefits of vaccination.  “Pfizer hadn’t even tested whether the vaccine stopped transmission,” Uthmeier said.

 

He said those allegations form the basis of the state’s lawsuit against Pfizer and Borla.  “That’s why we filed a lawsuit today against Pfizer and Albert Borla for their deceptive practices; what they did was wrong,” Uthmeier said.

 

Uthmeier framed the legal action as an effort to challenge what he described as a failure to provide Florida families with complete information about the vaccine.  “They assumed Florida families could not be trusted with the truth. Well, we disagree,” Uthmeier said.

 

He concluded by promising that his office would pursue accountability through the lawsuit.  “My office will hold them accountable. Thank you.”

 

Watch Uthmeier’s video statement below:

 

Rumble VIDEO: Pfizer’s Vaccine Messaging Heads to Court in Florida

 

[Posted by Talk Red

Published October 2, 2026

…MORE DESCRIPTION]

 

THE EXPOSÉ HOMEPAGE

SUPPORT THE EXPOSÉ

 

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BREAKING: Florida’s Attorney General SUES Pfizer and Albert Bourla for HIDING COVID Shot Deaths, Heart Damage, Miscarriages, and Strokes

The lawsuit alleges Pfizer hid safety signals, misled millions about transmission, and used deceptive marketing to drive maximum COVID shot uptake

 

By Nicolas Hulscher, MPH

October 1, 2026

FOCAL POINTS

 

Nicolas Hulscher, MPH on X

 

Florida Attorney General James Uthmeier has filed a sweeping lawsuit against Pfizer and its CEO, Albert Bourla, accusing them of deceiving the public about the safety and transmission-prevention capabilities of Pfizer’s COVID-19 mRNA injection.

 

The 49-page complaint was filed on October 1, 2026, in St. Lucie County, Florida, and targets Pfizer and Bourla personally under Florida’s Deceptive and Unfair Trade Practices Act.

 

The complaint opens with a striking line: “Those people are criminals.” That is how Bourla described people who publicly raised safety concerns about Pfizer’s COVID-19 injection.

 

At the center of the case is an explosive allegation: Pfizer publicly assured Americans that its COVID shot was safe while the company possessed internal and external safety information involving myocarditis, miscarriages, strokes, adverse events, and deaths.

Florida Sues Pfizer & Bourla (FOCAL POINTS PHOTO)

 

158,893 adverse events in just 10 weeks

 

According to the complaint, Pfizer’s own adverse-event database contained 158,893 adverse events from 42,086 case reports by February 28, 2021—only about 10 weeks after the vaccine received emergency authorization.

 

Yet in January 2023, Bourla publicly stated that Pfizer had seen “not a single [safety] signal” despite billions of doses having been administered.

 

Florida argues that statement was fundamentally incompatible with information already known about myocarditis and pericarditis.

 

1,223 reported deaths

 

The complaint also states that Pfizer’s database contained 1,223 reported fatalities following vaccination as of February 28, 2021.

 

Florida argues that the existence of this volume of serious adverse-event information undermined Pfizer’s sweeping public safety messaging.

 

The volume of reports became so large, according to the filing, that Pfizer hired 600 additional full-time employees and expected to hire another 1,800 workers to process adverse-event reports.

 

Pregnancy and miscarriages

 

Another major section of the lawsuit concerns pregnancy.

 

The complaint states that by February 28, 2021, Pfizer had reports involving 458 pregnant women exposed to its COVID vaccine. Of those reports, 248 involved an adverse event and 52 involved miscarriage, according to the filing. Nearly all of the reported miscarriages occurred during the first trimester.

 

The lawsuit also points to Pfizer’s planned clinical trial involving pregnant women.

 

Pfizer initially sought approximately 4,000 participants, but the complaint states that only 348 mothers and 335 infants were ultimately enrolled and that the study was terminated early. The women vaccinated in that study were 24–34 weeks pregnant, meaning the trial did not directly provide first-trimester vaccination data.

 

The complaint further cites the Comirnaty package insert as stating that there are no available data on use before 24 weeks sufficient to inform risks for major birth defects and miscarriage.

 

Pfizer pushed transmission claims without testing transmission

 

The second enormous pillar of Florida’s case concerns transmission. Pfizer and Bourla repeatedly told the public that vaccination would protect other people.

 

In December 2021, for example, Pfizer said that getting as many people vaccinated and boosted as possible remained the best course of action to “prevent the spread of COVID-19.”

 

But according to the complaint, Pfizer’s pivotal clinical trial did not test whether vaccination prevented person-to-person transmission.

 

The FDA itself stated in December 2020 that there was no evidence at that time that the vaccine prevented SARS-CoV-2 transmission from one person to another, and transmission was not an objective of Pfizer’s trial protocol.

 

A Pfizer executive later publicly acknowledged that the vaccine had not been tested for stopping transmission before entering the market.

 

Florida alleges that Pfizer nevertheless used the idea of protecting loved ones as a powerful marketing tool to increase vaccine uptake.

 

More than $80 BILLION in COVID vaccine revenue

 

The financial stakes were enormous. The complaint states that Pfizer turned approximately $1.5 billion in research and development spending into more than $80 billion in COVID vaccine revenue.

 

Pfizer’s vaccine captured nearly 70% of the U.S. and European COVID vaccine markets, according to figures cited in the complaint.

 

Meanwhile, Bourla received approximately $101.8 million in compensation from Pfizer between 2020 and 2023.

 

Florida’s complaint goes beyond safety claims and accuses Pfizer of engaging in broader unfair business practices to dominate the COVID vaccine market.

 

Florida wants the money back

 

Florida is seeking far more than a symbolic judgment. The Attorney General is asking the court for civil penalties, a permanent injunction against deceptive or unfair representations concerning Pfizer’s COVID vaccine, attorneys’ fees and other relief.

 

Most significantly, Florida is also seeking disgorgement—legal language meaning Pfizer could be forced to hand back profits connected to conduct the court ultimately determines violated Florida law.

 

Finally, a government is attempting to hold Pfizer and Albert Bourla accountable by at least some degree for their gross deception.

 

For years, the company’s false safety and transmission claims helped drive mass vaccine uptake. Now those fraudulent claims are headed to court.

 

Nicolas Hulscher, MPH

 

Epidemiologist and Foundation Administrator, McCullough Foundation

 

Support our mission: mcculloughfnd.org

 

Please consider following both the McCullough Foundation and my personal account on X (formerly Twitter) for further content.

 

© 2026 Peter McCullough MD MPH

FOCAL POINTS HOMEPAGE

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Monday, July 14, 2025

Pfizer – Big Pharma Evil

John R. Houk, Blog Editor

© July 14, 2025

 

Big Pharma is evil motivated by greedy profits more than the health of its customers. Don’t get me wrong, making a profit ethically is good individuals, Companies and Corporations all alike. BUT when that profit comes at the cost of harming human lives up to and including death, such a profit becomes evil.

 

Pfizer LIES about mRNA injections as “Safe & Effective” enters the realm of evil profit.

 

On 7/13 Telegram Natural News reposted its 7/10 website Natural News article by S.D. Wells entitled at the website, “HIGHLY CORRUPT PFIZER won’t release MYOCARDITIS study results because vaccine “safety” claim will obviously get blown out of the water”. Go to the website if you wish to check the source-links. I’m cross posting the Telegram version below.

 

THEN along the line “Pfizer is evil”, I’m sharing a Telegram Dr. Maria Hubmer-Mogg – MAHUMO post which excerpts 6-Minutes of a Naomi Wolf presentation it entitled, “PFIZER DOCUMENTS REVEAL THE GREATEST CRIME AGAINST HUMANITY”. I uploaded the video excerpt to my Rumble Channel which I share below the Natural News post.

 

This evil is more and more being exposed in slow-boat released documents and ever increasing peer-reviewed studies abandoning the Globalist-Science Narrative.

 

JRH 7/14/25

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HIGHLY CORRUPT PFIZER Won’t Release MYOCARDITIS Study Results

 

July 13, 2025

Telegram Natural News (Pt 1 & 2)

 

HIGHLY CORRUPT PFIZER won’t release MYOCARDITIS study results because vaccine “safety” claim will obviously get blown out of the water

 

Pfizer is facing growing scrutiny after delaying the completion of its post-marketing safety study on myocarditis and pericarditis in individuals under 21 who received its COVID-19 vaccine. Originally scheduled to be completed in 2024, the study’s new end date is November 2030 — eight years later than initially planned.

 

The delay has prompted accusations from medical experts and public health advocates of potential data suppression, especially in light of increasing evidence linking mRNA COVID-19 vaccines to heart inflammation in young people.

 

 • Pfizer has delayed completion of its myocarditis safety study in individuals under 21 to November 2030, sparking criticism over transparency and concern that interim findings — which have not been released — may reveal safety issues with its COVID-19 vaccine.

 

 • The study, involving 300 vaccinated participants and 100 controls, defines myocarditis cases only within seven days of vaccination, a narrow window that experts say could underestimate the true incidence compared to broader definitions used by the CDC and other health authorities.

 

• Updated FDA vaccine labels now warn of increased myocarditis risk, especially among males aged 16–25, with Pfizer and Moderna both required to include stronger language after mounting evidence from international and U.S. sources linked mRNA shots to heart inflammation.

 

• Multiple studies and adverse event reports, including VAERS data and international research, continue to show elevated myocarditis risks post-vaccination, fueling calls for greater scrutiny, transparency, and even moratoriums or bans on mRNA vaccines in some U.S. states.

 

Pfizer pushes deadline for study of myocarditis in kids and adults under 21

 

Launched in November 2022, the study is a collaborative effort with the U.S. National Heart, Lung, and Blood Institute. It follows 300 participants under age 21 who developed myocarditis or pericarditis after receiving Pfizer’s vaccine, with a control group of 100 individuals who developed similar conditions after a COVID-19 infection or related complications. Despite ongoing data collection, no interim results have been publicly released.

 

Critics argue that if the findings were positive, Pfizer would likely have already published them. Dr. Clayton J. Baker stated, “If their findings were reassuring, there would be a strong incentive to release them now.” Delaying results until 2030 while continuing vaccine administration, he said, is scientifically irresponsible.

 

Study design flaws have also been highlighted. Investigative journalist Sonia Elijah criticized the narrow definition of vaccine-related myocarditis — only counting cases diagnosed within seven days of vaccination. This contradicts other health guidelines. The CDC allows a 40-day window, while the Brighton Collaboration recognizes up to six weeks. VAERS data suggests symptoms can emerge up to 120 days post-vaccination. Elijah and others also noted the lack of an unvaccinated control group, making it harder to clearly establish causality.

 

Enrollment difficulties are another issue. Experts suggest Pfizer may be struggling to recruit enough participants, as noted by Dr. Jane Orient. With only 300 participants, the study lacks sufficient power to detect rare but serious side effects. Additionally, participant dropout over time could further undermine the study’s credibility.

 

Despite Pfizer’s delay, independent studies continue to link COVID-19 mRNA vaccines to increased heart inflammation risks. A South Korean study published in July 2024 found a 620% higher risk of myocarditis in vaccinated individuals. A 2024 UK study of 1.7 million children found myocarditis and pericarditis occurred only in vaccinated children. Likewise, a 2022 Nordic study involving 23.1 million people confirmed elevated myocarditis risk, especially among males aged 16 to 24.

 

In response to these findings, the FDA recently required stronger warning labels for Pfizer and Moderna vaccines. Current data show myocarditis occurs in about 8 cases per million doses for people under 65, with the highest rate — 38 per million — seen in males aged 16–25.

 

The CDC has acknowledged a causal link between mRNA vaccines and myocarditis since 2021. However, critics allege key data were withheld from the public, including early warnings from the Israeli Ministry of Health and redacted U.S. government reports obtained via FOIA.

 

With growing calls for accountability, some states like Idaho and Florida have moved to ban or restrict mRNA vaccine use. Experts and lawmakers continue to debate whether ongoing vaccination is justified given the known risks—especially as Pfizer’s key safety study remains unfinished for another five years.

 

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PFIZER DOCUMENTS REVEAL THE GREATEST CRIME AGAINST HUMANITY – Naomi Wolf

 

July 13, 2025

Telegram Dr. Maria Hubmer-Mogg – MAHUMO

 

Rumble VIDEO: PFIZER DOCUMENTS REVEAL THE GREATEST CRIME AGAINST HUMANITY – Naomi Wolf

 

[Posted by SlantRight

Published July 14, 2025]

 

Dr. Maria Hubmer-Mogg – MAHUMO Description:

 

Journalist Naomi Wolf claims internal Pfizer files expose massive fraud and cover-up:

 

👉 Pfizer KNEW by Nov. 2020 – just one month after rollout – that the vaccine had “failure of efficacy” and didn’t stop COVID.

 

👉 Pfizer’s own docs list COVID itself as the third most common side effect.

 

👉 By early 2021, Pfizer was so overwhelmed by adverse event reports, it had to hire 2,400 full-time staff just to process them.

 

👉 In May 2021, Pfizer documented heart damage in 35 minors – but the public wasn’t warned until four months later.

 

👉 Pfizer and the FDA knew the vaccine components didn’t stay at the injection site. They biodistributed to the brain, liver, spleen, adrenals, and ovaries.

 

👉 Lipid nanoparticles (industrial fats + polyethylene glycol) accumulate in female ovaries with no known way to remove them.

 

"The Pfizer documents contain evidence of the greatest crime against humanity in the history of our species."