Judicial Bombshell: Federal Judge Forces FDA to Release Over a Million Pages of Pfizer’s COVID-19 Trial Documents They Wanted to Keep Hidden for 75 Years

The United States District Court for the Northern District of Texas ruled against the Food and Drug Administration (FDA) in a high-profile case brought by the Public Health and Medical Professionals for Transparency (PHMPT).

The decision mandates the FDA to release the Emergency Use Authorization (EUA) file for the Pfizer-BioNTech COVID-19 vaccine no later than June 30, 2025.

The case stemmed from a Freedom of Information Act (FOIA) request by the PHMPT, which sought comprehensive data related to the Pfizer-BioNTech COVID-19 vaccine.

The FDA initially claimed it would need up to 75 years to process and release the requested documents. However, the Court, presided over by Judge Mark Pittman, rejected this argument, citing the importance of government accountability.

In late 2021, the U.S. Food and Drug Administration (FDA) faced significant public scrutiny after proposing a timeline that would extend the full release of documents related to the approval of Pfizer-BioNTech’s COVID-19 vaccine over several decades.

This proposal emerged following a Freedom of Information Act (FOIA) request by the Public Health and Medical Professionals for Transparency (PHMPT), a group of scientists and public health professionals seeking comprehensive data on the vaccine’s approval process.

The FDA initially suggested releasing 500 pages per month from a collection exceeding 300,000 pages, effectively delaying complete disclosure until around 2097. The agency cited limited staffing and the extensive volume of documents as reasons for this prolonged timeline.

In response to the backlash, U.S. District Judge Mark Pittman in Fort Worth, Texas, issued a ruling in January 2022 that significantly shortened the FDA’s proposed timeline.

Judge Pittman ordered the agency to release 55,000 pages per month, ensuring that all documents would be made public by the end of September 2022.

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DNA Contamination In Pfizer COVID Vaccines Up To Four Times Legal Limits, Study Finds

Researchers found DNA in Pfizer’s COVID-19 vaccines at levels three-to-four times higher than regulatory limits, according to a new “bombshell” study.

“This far exceeds the maximal acceptable concentration of 10 ng [nanograms] per clinical dose that has been set by international regulatory authorities,” the authors wrote.

The peer-reviewed study, published this week in the journal Science, Public Health Policy and the Law, also found simian virus 40 (SV40) DNA contaminants in the vaccines. And the researchers determined that the spike proteins produced by the vaccines persist in the body longer than claimed.

The findings led the authors to call for “an immediate halt of all RNA biologicals.”

Karl Jablonowski, Ph.D., senior research scientist at Children’s Health Defense (CHD), told The Defender that DNA contamination may contribute to the increase in autoimmune diseases among the vaccinated. “The immune system operates on very sensitive detections to initiate responses,” he said.

“DNA suddenly deposited into your bloodstream could kickstart the interferon response,” Jablonowski said. “The interferon response, when there’s nothing to find but ‘self,’ could be the springboard for autoimmune disease.”

The study also showed that the spike proteins produced after vaccination persist in the body for at least seven days following vaccination instead of the shorter period Pfizer-BioNTech previously claimed. The spike proteins are also prone to shedding.

These results “raise grave concerns” about mRNA vaccines, the study concluded.

Kevin McKernan, founder of Medicinal Genomics, is the first scientist who identified the presence of SV40 in the mRNA vaccines. He called the new study “a tour de force on the DNA contamination topic.” McKernan wrote about the study on Substack, and said in an X post that the study’s authors “knocked it out of the park.”

Immunologist and biochemist Jessica Rose, Ph.D., agreed. “This paper is the paper of the century. The paper is not only a work of art in terms of the study layout. It is very well-written and settles ongoing ‘issues’ pertaining to allegations made by regulatory bodies that the DNA contamination issue is misinformation,” Rose said.

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Nobel Peace Prize Nominee Provides Affidavit: “All covid 19 vaccine mRNA gene therapies are BIOWEAPONS which means they are POISON”

A former Nobel Peace Prize nominee, Dr. Ben Marble, M.D., creator of MyFreeDoctor.com provided an affidavit stating that “All covid 19 vaccine mRNA gene therapies are BIOWEAPONS which means they are POISON”.

Dr. Ben Marble is the inventor of the Hands Free Toothbrush & Asynchronous Telemedicine and Founder Of MyFreeDoctor.com. Dr. Ben Marble is also the first MD to treat patients for free in all 50 States and has successfully treated ~25,000 covid 19 patients.

Dr. Ben Marble is the eighth expert to file an affidavit in a new legal case seeking an injunction to prohibit COVID-19 and mRNA injections in the state of Florida because they are bioweapons. Affidavits were also provided by Francis Boyle, J.D., PhD; Karen Kingston; Ana Mihalcea, M.D., PhD; Rima Laibow, M.D.; Andrew Zywiec, M.D.; Marivic Villa, M.D., and Avery Brinkley, M.D.

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Bombshell US House investigative report confirms that almost everything the alternative media said about COVID origins, lockdowns, masks, vaccines and government overreach was TRUE

So four years after the COVID pandemic nightmare was unleashed upon America by a cabal of junk science tyrants and power-hungry vax-o-crats, the US House has just released a damning, detailed investigative report that reveals the independent media was right all along.

COVID was engineered in a lab.

Mask demands and vaccine mandates were based on junk science.

Lockdowns were completely made up by self-appointed scientism authoritarians.

The government covered up the truth and pushed disinformation propaganda on purpose.

Dr. Fauci and others were guilty as hell.

So all the censorship by Big Tech turns out to be truly malicious and even harmful to the public. And the entire corporate media was nothing but an organized cabal of liars and profiteers… brought to you by Pfizer.

This investigative report reveals that COVID was a crime scene, and the government conspired with Big Tech and mainstream media to commit numerous crimes of cognitive assault (psyops), medial violence (vaccines) and hospital homicide against the American people.

So when do the mass arrests begin? (Don’t hold your breath.)

Unfortunately, no one can bring back the estimated 1.2 million Americans who were killed by the jabs because they “believed the science.”

Fortunately for you and I, we never believed the plandemic hype in the first place, and we most certainly didn’t follow the herd into getting jabbed, masked and locked down.

It turns out that was a tremendously valuable choice of actions on our part.

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11 Countries Demand Immediate Suspension of COVID-19 Modified mRNA Vaccines

On Monday, Ireland joined an international group of hundreds of politicians, medical experts, and other professionals who wrote to the heads of state of 10 other European countries “calling for a suspension of modified mRNA vaccines citing serious health concerns,” according to a press release from NORTH Group.


“Ireland joined this initiative today, with support from experts including Professor Francis Boyle, author of the U.S. ‘Biological Weapons Anti-Terrorist Act of 1989,’” the announcement reads.

NORTH Group’s letter of concern is “co-signed by physicians, scientists, politicians, and other qualified professionals” from around the world.

The countries listed now include: Ireland, Greenland, Iceland, the U.K., Norway, Denmark, Sweden, Finland, Latvia, Estonia, and Lithuania.

The missive calls for the “immediate suspension of COVID-19 modified mRNA vaccines and an investigation into the presence of excessive levels of residual DNA in multiple vials, which is a serious, unquantified risk to human health,” according to a summary document.

“As an international group of politicians and qualified professionals, we are gravely concerned about the effects of COVID-19 modified mRNA vaccines on our populations and call for their immediate suspension,” the letter reads.

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BioNTech RNA-Based COVID-19 Injections Contain Large Amounts Of Residual DNA Including An SV40 Promoter/Enhancer Sequence

Background: BNT162b2 RNA-based COVID-19 injections are specified to transfect human cells to efficiently produce spike proteins for an immune response.

Methods: We analyzed four German BNT162b2 lots applying HEK293 cell culture, immunohistochemistry, ELISA, PCR, and mass spectrometry.

Results: We demonstrate successful transfection of nucleoside-modified mRNA (modRNA) biologicals into HEK293 cells and show robust levels of spike proteins over several days of cell culture. Secretion into cell supernatants occurred predominantly via extracellular vesicles enriched for exosome markers. We further analyzed RNA and DNA contents of these vials and identified large amounts of DNA after RNase A digestion in all lots with concentrations ranging from 32.7 ng to 43.4 ng per clinical dose. This far exceeds the maximal acceptable concentration of 10 ng per clinical dose that has been set by international regulatory authorities. Gene analyses with selected PCR primer pairs proved that residual DNA represents not only fragments of the DNA matrices coding for the spike gene, but of all genes from the plasmid including the SV40 promoter/enhancer and the antibiotic resistance gene.

Conclusion: Our results raise grave concerns regarding the safety of the BNT162b2 vaccine and call for an immediate halt of all RNA biologicals unless these concerns can be dispelled.

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Fauci admitted to RFK Jr. that none of 72 mandatory vaccines for children has ever been safety tested

Robert F. Kennedy Jr., President-elect Donald Trump’s nominee to head the Department of Health and Human Services (HHS), recently recounted how when threatened with a lawsuit, Dr. Anthony Fauci finally had to eat his words and admit that none of the 72 vaccines currently mandated for children in the U.S. has ever been safety tested.

“For many years, I was saying that not one of the 72 vaccines mandated for children has ever been safety tested in pre-licensing, placebo-controlled trials,” began Kennedy, speaking at a Hillsdale College event. “Not one.”

Fauci went so far as to call Kennedy “a liar.”

When then-President Trump appointed Kennedy to run a vaccine safety commission, Trump ordered Fauci and Collins to meet with him along with White House counsel present.

Kennedy told Fauci, “You say I’m lying. For eight years you’ve been saying I’m lying,” and challenged Fauci to “show me the study” which shows that the multitude of vaccines America’s children are required to receive have been safety-tested.

Fauci claimed that he didn’t have it with him. “It’s back in Bethesda. I’ll send it to you.”

“I never got it,” said Kennedy, “so I sued him.”

“After stonewalling us for a year, their lawyers met us on the courthouse steps and said, ‘Yup, you’re right. We never had any study,’” said Kennedy.

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Pfizer pregnancy trial showed the COVID shots increased AESIs (like major congenital abnormalities) in newborns by over 4X

Pfizer recently updated the results of their randomized clinical trial of the COVID shots on pregnant women entitled “To Evaluate the Safety, Tolerability, and Immunogenicity of BNT162b2 Against COVID-19 in Healthy Pregnant Women 18 Years of Age and Older. ClinicalTrials.gov ID NCT04754594.

This prompted me to have a second look at these results which were first posted on July 14, 2023, over a year ago.

Did you know that the study showed that if you were assigned the vaccine, your child had a stunning 4.2X higher rate of AESIs such as MAJOR congenital abnormalities and developmental delays in just the first 6 months after birth?

Because the trial enrolled fewer women than planned, the effect size reached only the 90% level of significance. Based on just this trial, we are 90% certain that the vaccines made things worse. However, when you look at other data, the certainty approaches 100%.

4.2X is jaw dropping for an effect size for these types of major birth defect adverse events.

Was there a benefit? Nope. Moms in both groups got the same number of COVID infections (2 in each group). Vaccine efficacy estimated at a measly 3.8 (because the groups were different sizes). A perfect vaccine is 100. A vaccine which does nothing is 0. The 3.8 value was both tiny and NOT statistically significant. It’s entirely possible that the vaccine increased your risk of getting COVID. We can’t tell from the study.

This was all known more than 5 months ago when the results were first posted.

Why didn’t the CDC warn women that they were wrong?

This double-blinded placebo controlled trial which is considered to be the best evidence in medicine shows that it’s 90% likely it made things worse.

It’s Pfizer’s own data published on Clinical Trials.gov using gold-standard DB-RCT methodology. Anyone can analyze it. It’s in plain sight. Doesn’t get any better than this.

Today, more than 5 months after the lack of any COVID benefit was published on the NIH website (clinicaltrials.gov), the CDC is still silent on this.

Is the entire medical community blind, ignorant, or just corrupt? NOT A SINGLE MAINSTREAM doctor is speaking out. NOT ONE.

Dr. James Thorp got fired for speaking out about the vaccine harms to pregnant women so he’s not mainstream anymore since he’s out of the system. One of the few honest doctors and he gets fired. What does that tell you? His research which has been published in peer-reviewed journals, confirms the results of the Pfizer trial. In spades.

We have a very corrupt medical system where everyone is afraid to tell the truth.

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How RFK Jr. could use levers of HHS to shape vaccine and drug outcomes

Robert F. Kennedy Jr. could use Health and Human Services’ vast bureaucracy to put a distinct stamp on vaccine policy, drug approvals and food regulation if he’s confirmed. But with so many legal requirements and bureaucratic layers baked into the process, it’s hardly a foregone conclusion he will.

Why it matters: Experts say RFK Jr.’s public calls for more transparency and vows to shore up the trustworthiness of federal health agencies may translate into more requests for vaccine safety data and into appointing like-minded individuals to advisory panels that could influence coverage of drugs, services and devices.

  • They also say it could result in shifting public health funding to chronic disease or environmental health and away from infectious disease, or a diversion of federal investment to study unproven health issues instead of known risks.
  • And they’re expecting attempts to remove job protections from career federal employees who work in policymaking roles and reduce the ranks of officials who don’t align with RFK Jr.’s goals.

Between the lines: In the near term, he’s likely to focus on how much influence he might exert on negotiations between the Food and Drug Administration and the health industries it regulates over user fees for companies, which fund a significant portion of the FDA’s operations.

  • Talks to reauthorize programs for prescription drugs, medical devices and generics are due to start next year and could provide a crucible for Trump appointees to take aim at what they describe as regulators’ coziness with industries they police.
  • The spotlight could fall especially hard on vaccines, based on Kennedy’s criticisms of the federal pandemic response, his calls to revoke emergency use authorizations for COVID shots and his advocacy of hydroxychloroquine and ivermectin, both of which were found ineffective for treating the virus.

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America’s Compliance with Federal Vaccine Recommendations Has Collapsed

A new Centers for Disease Control and Prevention report titled, Influenza, COVID-19, and Respiratory Syncytial Virus Vaccination Coverage Among Adults — United States, Fall 2024, found that, by November 9, 2024, only an estimated 17.9% of adults aged ≥18 years had received the updated COVID-19 booster injection. Approximately 13.5% of adults indicate that they “definitely will get vaccinated.” This means that the vast majority of Americans reject novel genetic booster shots designed on a computer screen with no human data. These estimates were derived using a ‘nondecreasing composite estimation procedure’ combining completed interviews from the current and previous weeks. Because the data are self-reported, they are subject to recall or social desirability bias, which could result in overestimation of true uptake. In other words, true COVID-19 booster uptake may be even lower.

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