Tag: pfizer

VAX EYE SYNDROME: Pfizer COVID vaccine spike prions enter the EYES and CORNEA, causing serious damage

The researchers focused on the corneal endothelium, the innermost layer of the cornea responsible for maintaining corneal clarity by pumping out excess fluid. Using specialized tools such as specular microscopy and Sirius corneal topography, they observed changes in corneal thickness, a decline in endothelial cell count and alterations in cell size and shape — indicators of stress or damage to this delicate structure.

Specifically, corneal thickness increased by approximately 14 micrometers (a 2 percent rise), which in itself is not harmful but could signal inflammation or fluid retention. More concerning was the eight percent drop in endothelial cell density — from 2,597 to 2,378 cells per square millimeter — still within the safe range for healthy individuals, but potentially risky for those with already compromised eye health.

The study also found that the vaccine led to increased variability in cell size, known as the coefficient of variation, which rose from 39 to 42. This suggests some cells may have died and others stretched to fill the gaps, a typical response to stress. Additionally, the percentage of hexagon-shaped cells, which are vital for maintaining a healthy endothelial layer, dropped slightly from 50 percent to 48 percent.

Although none of the participants reported noticeable vision issues during the two-month follow-up, scientists caution that these microstructural changes could have long-term consequences, especially for people with existing eye problems or a history of eye surgeries such as corneal grafts. If the damage to the endothelium is permanent or worsens over time, it could result in conditions like corneal edema, bullous keratopathy or corneal decompensation — disorders that may lead to chronic vision impairment or even blindness if untreated.

Despite these findings, the researchers did not advise against COVID-19 vaccination. They emphasized the need for ongoing monitoring and further long-term studies to determine if the observed changes persist or resolve over time. Importantly, the study confirmed a high likelihood that the changes were directly associated with the vaccine and not random occurrences.

This research adds to a growing list of safety concerns surrounding COVID-19 vaccines. In May, the U.S. Food and Drug Administration expanded warning labels on Pfizer and Moderna vaccines to more clearly highlight the risk of myocarditis and pericarditis, particularly in young men aged 16–25.

While the short-term effects of the Pfizer vaccine on eye health appear to be mild, the study underscores the importance of ongoing post-vaccination surveillance and personalized medical care for individuals at risk. As evidence continues to evolve, health agencies and physicians may need to consider more tailored guidance for those with existing ocular conditions.

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Ghost Shot: Pfizer quietly admits it will never manufacture original FDA approved COVID vaccines

The August 23, 2021 FDA approval of Pfizer’s Comirnaty vaccine was a cause for celebration. Marked as a turning point in the battle against COVID19, the announcement was highly publicized by the Biden Administration with the clear intention to extinguish “vaccine hesitancy” and boost uptake.

It was celebrated as a cause for national relief, and many Americans arrived at their local pharmacies under the impression, via government and pharmaceutical propaganda, that they were receiving an FDA-approved COVID vaccine. Yet that legally distinct product, as we know it, never existed. And now we know, via Pfizer, that it will never exist.

For the uninitiated:

Comirnaty is a legally distinct product from the emergency use authorization (EUA) shots, and It has never made its way to market. For months on end, no such vaccine has ever become available. Those who received the “Pfizer shot(s)” have been injected with the emergency use authorization (EUA) version of the shots.

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3 New Plaintiffs Ask to Join COVID Vaccine Injury Lawsuit Against Bill Gates

Three COVID-19 vaccine injury victims are asking to join a Dutch lawsuit against Bill Gates, Pfizer CEO Albert Bourla and 15 other defendants, alleging they misled the public about the safety of the COVID-19 vaccines.

The lawsuit was filed last year by seven COVID-19 vaccine injury victims, one of whom has since died.

According to a filing by the plaintiffs’ attorney, Peter Stassen, the three new victims “were healthy people” who began experiencing health problems after receiving mRNA COVID-19 vaccines.

“The applicants are of the opinion that the serious side effects that occurred after having the Covid-19 (mRNA) injections are the direct result of the content / composition of these Covid-19 (mRNA) injections,” the filing states.

Doctors have repeatedly refused to diagnose a link between vaccination and their injuries, Stassen said.

During a hearing today at the District Court of North Netherlands in Leeuwarden, Stassen also asked the court to approve five expert witnesses who will testify about the risks and dangers of the COVID-19 shots:

  • Catherine Austin Fitts, founder and publisher of the Solari Report and former U.S. assistant secretary of Housing and Urban Development.
  • Sasha Latypova, a former pharmaceutical research and development executive.
  • Joseph Sansone, Ph.D., a psychotherapist who is litigating to prohibit mRNA vaccines in Florida.
  • Katherine Watt, a researcher and paralegal.
  • Mike Yeadon, Ph.D., a pharmacologist and former vice-president of Pfizer’s allergy and respiratory research unit.

Another proposed witness, Francis Boyle, J.D., Ph.D., who agreed in January to testify on behalf of the plaintiffs, has since died. Boyle was a professor of international law at the University of Illinois and a bioweapons expert who drafted the Biological Weapons Anti-Terrorism Act of 1989.

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Pfizer bribery probe dropped after ex-company lawyer Pam Bondi takes over DOJ in February 2025.

The DOJ dropped its Pfizer bribery probe in China and Mexico soon after Pam Bondi, a former Pfizer legal consultant, became Attorney General in February 2025. The investigation’s closure, evident from Pfizer’s latest filings, has raised concerns about Bondi’s influence and DOJ impartiality.

For the past several years, pharmaceutical giant Pfizer has been under investigation by the U.S. Department of Justice for potential foreign corruption violations related to its activities in China and Mexico, according to the company’s financial filings.

But that appears to have changed after the Trump administration tapped Pam Bondi — previously an outside legal counsel for Pfizer — to lead the Justice department as attorney general.

In the company’s most recent annual report, filed three weeks after Bondi took office in early February, there was no longer any reference to the Justice Department investigations into the company’s potential violation of the Foreign Corrupt Practice Act. A quarterly a report in May also contains no reference to these investigations.

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Pfizer’s Delayed Myocarditis Study

This headline has garnered so much attention on social media that I was asked to participate in an interview last night to discuss the topic. First, I had to clarify that I cannot be interviewed about ACIP issues without prior clearance from HHS Communications. Once that was understood, at 6:00 PM (dinner time!) I dialed in via Zoom, and we talked on the record. No, I do not know if or when the interview will be aired. Before the interview, as usual, I did the necessary diligence to avoid embarrassing myself due to ignorance, keeping in mind the first rule of social media.

It is often better to stay quiet and have people wonder if you are ignorant than to tweet and remove all doubt.

Let’s dive into the details. I think that this particular situation provides a great example of how bias, combined with insufficient background and subject matter experience, can lead to unjustified clickbait headlines. This is a chronic problem on both sides of the mRNA “vaccine” safety debate, one which makes it so, so much harder to get to the bottom of all of this.

I will try to explain so that most can understand, but it may get a little technical. The nuances of clinical research study design and implementation are complicated. Please try to stick it out, if for no other reason than it does lead back to some statements from CDC’s Captain Dr. Sarah Meyer (CDC/NCEZID) during her recent presentation titled “COVID-19 safety update” regarding long-term outcomes from COVID-19 mRNA product myocarditis. Consider that an embedded easter egg.

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71st Bilderberg Meeting Agenda and Attendees REVEALED

The clandestine Bilderberg Group’s 71st annual meeting kicks off on Thursday, where 120-140 heads of state, industry, media, finance and technology will convene to plot global policy behind closed doors.

Bilderberg’s 2025 confab will be held June 12-15 in Stockholm, Sweden, at the Grand Hotel.

While the organization on its face appears powerless, the secretive group – whose discussions are held under Chatham House rules – has been accused of steering world events, including the creation of the European Union and its euro single currency. It’s even rumored to have helped install heads of state like former US Presidents Bill Clinton and Barack Obama and UK Prime Minister Tony Blair, all of whom reportedly attended Bilderberg prior to their rise.

Other attendees have included top media figures from outlets like The New York Times, Politico, The Atlantic, The Washington Post, The Economist, The Guardian and more, making it all the more bizarre that the convention receives little to no press coverage each year.

Via The Nordic Times:

The public denied for a long time that the meeting was organized, or even existed, and was dismissed in the mainstream media for many years as a “conspiracy theory”. In the 21st century, as a result of independent media coverage, it has since been recognized that the meeting has actually been taking place since 1954, with high-profile lists of participants typically ranging from 120-150 specially invited participants.

Check out the full list of attendees and key discussion topics below, via BilderbergMeetings.org. This year’s conference includes such key figures as Palantir’s Alex Karp, Pfizer CEO Albert Bourla, CNN’s Fareked Zakaria, and Economist editor-in-chief Zanny Minton Beddoes, to name a few.

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FDA Forces Moderna and Pfizer to Admit Covid “Vaccines” Cause Lasting Heart Damage in Young Males

For years, parents and medical professionals have sounded the alarm about the dangerous link between mRNA COVID-19 vaccines and heart inflammation in young males—only to be dismissed as “anti-vaxxers” or conspiracy theorists. Now, in a stunning reversal, the U.S. Food and Drug Administration (FDA) has ordered Pfizer and Moderna to strengthen their warning labels, finally admitting that these shots can cause long-lasting heart damage, particularly in adolescent boys and young men.

But this admission comes far too late—after millions of doses were administered under false pretenses, after countless young lives were altered by myocarditis, and after public health agencies actively suppressed the truth. The FDA’s belated action raises a critical question: How many more injuries could have been prevented if the government had prioritized transparency over blind vaccine promotion?

Key points:

  • The FDA has mandated that Pfizer and Moderna update their COVID-19 vaccine labels to include stronger warnings about myocarditis and pericarditis, particularly in males aged 16 to 25.
  • New data reveals that myocardial injury is often long-lasting, contradicting earlier CDC claims that heart inflammation “tends to resolve quickly.”
  • The highest incidence of myocarditis occurs in young males, with 38 cases per million doses—far higher than previously acknowledged.
  • Internal government emails show that health officials deliberately avoided warning the public about these risks, even after detecting safety signals in 2021.
  • The FDA’s action follows a Senate investigation exposing how federal agencies downplayed and hid vaccine injuries.

A long-overdue admission of harm

For years, independent researchers and medical professionals warned that mRNA vaccines posed a disproportionate risk to young, healthy individuals—especially males. Yet, public health agencies dismissed these concerns, insisting that the benefits outweighed the risks. Now, the FDA has been forced to acknowledge what health freedom fighters have said all along: These vaccines can cause serious, sometimes permanent, heart damage.

The updated labels must now state that myocardial injury is common among those who develop post-vaccination myocarditis, with data showing persistent damage five months after vaccination. This directly contradicts the CDC’s previous assurances that cases were “mild” and “resolved quickly.”

Why did it take so long? Internal documents obtained through FOIA requests reveal that as early as May 2021, the CDC and FDA considered issuing a public warning but ultimately chose silence over transparency.

The suppression of truth and the cost of deception

The Senate’s Permanent Subcommittee on Investigations recently released a damning report exposing how federal health agencies systematically concealed the myocarditis risk linked to COVID-19 vaccines. Internal emails reveal that officials engaged in a coordinated cover-up by refusing to update the V-safe reporting system to include cardiac symptoms, ensuring countless cases were never documented. Additionally, they blocked a planned Health Alert Network warning that would have alerted doctors and the public to the dangers, prioritizing public perception over transparency.

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Jim Jordan probes politics of Pfizer COVID vax trial as research suggests jabs hurt fertility

The political pressures around clinical trials for COVID-19 vaccines in the 2020 presidential campaign first drew scrutiny from Democrats, with then-nominees Joe Biden and Kamala Harris spreading mistrust of Operation Warp Speed and suggesting they would avoid jabs developed in the Trump administration.

The parties largely switched sides in the Biden administration, with then-Vice President Harris claiming it was “starting from scratch” on a vaccine strategy and even mandating vaccinations for her own campaign employees once she replaced Biden at the top of the 2024 ticket.

Yet Republicans have continued claiming Operation Warp Speed saved millions of lives based on modeling studies, amid five years of global research on severe adverse events in certain groups following COVID vaccination, from heart inflammation to neurological disorders, and the jabs’ mediocre-to-negative performance against infection.

House Judiciary Committee GOP leaders seized on new evidence Thursday that Pfizer withheld what it considered positive trial results until after the 2020 election, with the result that President Trump couldn’t take credit for a finished vaccine, giving Republicans something to unite around amid internal divisions over the pace of reversing Biden’s COVID vaccine policies.

The Department of Health and Human Services is reportedly planning to stop recommending routine COVID vaccines for pregnant women, teens and children, more than 100 days into the Trump administration and after new peer-reviewed research suggests COVID vaccines worsen fertility and mRNA jabs specifically can produce spike protein for up to eight months.

Yet another peer-reviewed study this year, published in the Endocrine Society’s Journal of Clinical Endocrinology and Metabolism, found the risk of underactive thyroid “significantly increased from 6 to 12 months” after vaccination, and that both under- and overactive thyroid was “significantly elevated at 12 months” for mRNA vaccine recipients specifically.

The Taiwanese researchers “used a huge database, carefully matched vaccinated and unvaccinated patients, and followed outcomes for a full year,” former New York Times drug industry reporter Alex Berenson wrote. “That combination gave the study very strong statistical power, meaning that its findings are probably not the result of chance.”

“25,000 children a day are getting the latest version of the mRNA shot,” Texas doctor Mary Talley Bowden, an early victim of COVID treatment policing whose litigation prompted the FDA to stop demonizing ivermectin on social media, wrote on X Friday.

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Pfizer’s election meddling exposed: Top scientists weaponized science to sway the 2020 vote, so they could benefit from unlawful mandates

In the high-stakes world of corporate power and political manipulation, few revelations strike as deeply as the allegation that Pfizer executives deliberately slowed COVID-19 vaccine trials to influence the 2020 U.S. election. Newly uncovered testimony suggests that top Pfizer R&D leaders orchestrated a delay in clinical testing—not for scientific caution, but to ensure results wouldn’t emerge before Election Day. This bombshell, revealed through congressional investigations, paints a damning picture of a pharmaceutical giant willing to play god with public health for political and financial gain. The implications are staggering: a company entrusted with saving lives instead weaponized its science, suppressed critical data, and helped shape an election that led to unprecedented medical coercion.

Key points:

  • Congressional investigators allege Pfizer intentionally slowed vaccine trials to avoid influencing the 2020 election.
  • Former Pfizer scientist Dr. Philip Dormitzer reportedly admitted the delay was orchestrated by senior R&D leaders.
  • The timing allowed Pfizer to avoid scrutiny before the election, then rapidly deploy mandates under a new administration.
  • The scheme backfired as vaccine failures and injuries mounted, exposing the fraud behind the rushed approvals.
  • The investigation raises urgent questions about corporate collusion, government corruption, and the erosion of medical ethics.

The election interference playbook

The 2020 presidential race was already one of the most contentious in U.S. history, with COVID-19 lockdowns, mask mandates, and promises of a “miracle” vaccine dominating the national conversation. Internal documents and whistleblower testimony now suggest Pfizer executives saw an opportunity—not to serve public health, but to exploit it. According to GSK’s testimony to Congress, Dr. Philip Dormitzer, a former Pfizer R&D leader, revealed that the company’s top three scientists deliberately slowed trial progress to avoid releasing data before November.

Dr. Dormitzer had told GSK employees that “in late 2020, the three most senior people in Pfizer R&D were involved in a decision to deliberately slow down clinical testing so that it would not be complete prior to the results of the presidential election that year.”

This wasn’t about scientific rigor—it was about political timing. Had Pfizer released results in October, then-President Donald Trump could have claimed credit for Operation Warp Speed, potentially swaying voters eager for an end to pandemic restrictions. Instead, Pfizer’s calculated delay left the public in limbo, fueling frustration and anger that Democrats weaponized against Trump. By the time the vaccine was unveiled under the Biden administration, the groundwork had been laid for aggressive mandates, despite mounting evidence of the shot’s inefficacy and risks.

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Pfizergate: Top European Court Slams Corrupt Globalist EU Chief Von der Leyen in Bombshell Ruling Over Secret Covid-19 Vaccine Procurement Texts

In a ruling that’s shaken the corrupt foundations of the European Union, the EU’s top court has declared that Commission President Ursula von der Leyen broke transparency rules by hiding secret text messages she exchanged with Pfizer CEO Albert Bourla—just as the EU was locking itself into the biggest vaccine deal in its history.

The judgment, handed down by the European Court of Justice (ECJ), exposes a damning breach of public trust and fuels the growing outcry over what critics have dubbed “Pfizergate”—a scandal that underscores everything wrong with the unaccountable EU bureaucracy, Big Pharma’s grip on policy, and von der Leyen’s corrupt, authoritarian style of rule.

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