The Pfizer Papers: What They Didn’t Want You to Know

A team of 3,250 professionals has analyzed over 450,000 pages of Pfizer’s internal documents covering its trials for its mRNA vaccine, revealing a wealth of information that deeply challenges the narrative we have been given by Pfizer’s representatives and the media. These documents, now scrutinized and compiled in “The Pfizer Papers: Pfizer’s Crimes Against Humanity,” (edited by Naomi Wolf) paint a disturbing picture of what seems to be the largest medical fraud in history.

A History of Ethical Quandaries

Pfizer’s ascent to the forefront of the COVID-19 vaccine race was not without challenges. The shadows of past controversies, like the 1990s Nigerian meningitis trial, loom large. Five children died after receiving an experimental antibiotic, raising haunting questions about ethical standards in clinical trials, especially in vulnerable populations.

In 2020, we find ourselves immersed in yet another complex ethical dilemma. Pfizer began their clinical trials in December of 2020 in an effort to have the FDA grant them Emergency Use Authorization, which essentially would allow Pfizer to bypass the normal 10 to 12-year period normally required for the development and approval of a new vaccine. 

“The basis for scientific inquiry is transparency. Without it, we’re not practicing science; we’re engaging in blind faith.”

~ Anonymous Researcher

The Battle for Transparency

In a twist that reads like a legal thriller, a group of scientists and medical professionals found themselves locked in a courtroom battle with the FDA. Attorney Aaron Siri sued the FDA to have the results of Pfizer’s 90-day trials released to the public. In a move that shocked many, the FDA asked the judge to keep the secret documents private for 75 years. Had the judge granted their request, most individuals negatively impacted by the Pfizer trials would have died before the public even knew that anyone had been injured from the Pfizer vaccine.

This raises the following questions:

  • Why did a federal agency act as a proxy for a multi-billion dollar pharmaceutical company?
  • Why did the FDA, which is supposed to protect the people from corporate greed, instead try to shield Pfizer from accountability to the people?
  • What was the FDA hiding? What did Pfizer and the FDA not want you to know?

Fortunately, the judge did not grant the FDA’s request and instead released the documents to the public. This victory for transparency advocates underscores a growing demand for accountability in public health decisions.

The Efficacy Lie

According to the book, the Pfizer documents reveal that Pfizer knew with certainty within 90 days of the rollout that their vaccine was not effective in preventing COVID infection. The documents consistently use the terms “vaccine failure” and “failure of efficacy,” which contrast sharply with the public narrative of 100% efficacy (later deceptively changed to 95% to give the false impression that, while it wasn’t completely effective, it was still largely effective).

The documents paint a concerning picture of how the vaccine’s components—mRNA and spike protein—distribute throughout the body. The Pfizer documents reveal that Pfizer knew very well that the vaccine quickly spread to the organs of the body within the first 48 hours. Contrary to Pfizer’s public claims, the mRNA and spike protein did not remain in the deltoid muscle after injection.

Within 48 hours of injection, these elements spread far beyond the injection site, accumulating in organs like the liver, adrenals, spleen, brain, and ovaries (in women). Pfizer was even aware that their vaccine crossed all membranes in the body, including the blood-brain barrier. This systemic distribution raises questions about potential long-term effects on various organs, particularly regarding inflammatory responses or other adverse effects linked to the presence of spike proteins in tissues outside the immune response context.

Modification Without Notifying the Public

According to this new book, the documents clearly show that Pfizer made changes to the composition of the vaccine, after the trials finished, without any public disclosure or clinical trials. The contents of the vaccine given to the public were different from the vaccine administered during clinical trials, yet Pfizer never informed the public of this change, meaning that the public were now unwitting test subjects for Pfizer’s untested, post-trial, revised vaccine.

The Human Cost: A Litany of Adverse Effects

According to the book, the sheer volume of adverse event reports in the Pfizer documents is staggering. Pfizer hired 2,400 new employees to process the inundation of adverse effect reports in their Worldwide Safety database. This speaks volumes about the scale of the issue.

Pfizer knew by February of 2021 that their vaccines produced a large number of adverse events, including:

  • Death
  • SevereCovid-19
  • Liver injury
  • Neurological adverse events such as dementias, tremors, Alzheimer’s, Parkinson’s, and epilepsies.
  • Facial paralysis
  • Kidney injury
  • Autoimmune diseases
  • Multiple-organ dysfunction syndrome
  • Respiratory issues and damaged lung structure
  • Arthritis-type joint pain
  • Blood disorders include blood clots, lung clots, leg clots, and thrombotic thrombocytopenia.
  • Vasculitis
  • Heart conditions including myocarditis, pericarditis, tachycardia, and arrhythmia.

According to the book, by April of 2021, Pfizer was fully aware that their mRNA vaccine caused heart problems in young people, but they did not communicate this information to the public.

Perhaps the most heartbreaking revelations concern the effects on pregnant women and infants. Adverse events occurred in more than 54% of cases where pregnant mothers received vaccinations. Alarmingly, 53 spontaneous abortions occurred as a result of vaccination. Two newborns died, and some of the newborns suffered severe respiratory distress after ingesting breast milk from vaccinated mothers.

The documents reveal troubling adverse events in children under 12, including strokes, facial paralysis, and kidney injury or failure. These serious conditions plagued many of the infants and children under 12 who received vaccinations in the trials. These findings raise serious questions about the wisdom of vaccinating young children—a demographic at relatively low risk from COVID-19 itself.

Falsifying and Manipulating Data

Allegations of data manipulation call into question the integrity of the entire vaccine development process. The Pfizer Papers reveals that there were more deaths in the vaccinated group than there were in the placebo group, but Pfizer falsified this data when submitting it to the FDA and instead claimed that more people had died in the placebo group. This purported manipulation of data undermines scientific integrity and prompts significant inquiries about the vaccine’s actual safety profile.

The FDA’s failure to inspect key trial sites, despite whistleblower complaints, raises alarming questions about regulatory oversight. This apparent lapse in due diligence undermines public trust in the very institutions tasked with ensuring vaccine safety. The fact that a federal agency may have been covering for a multi-billion dollar pharmaceutical company is a serious concern that demands further investigation.

Unwitting Test Subjects

Many individuals who received the vaccines at this time were unaware that they were taking an experimental gene therapy, which had not only circumvented the standard 10-year approval and development process, but also concealed its clinical trials from the public. These unwitting and trusting individuals were unaware that they were the actual test subjects, and that previous trials had led to numerous adverse events and deaths.

They were completely unaware that these multi-billion dollar pharmaceutical companies had been given complete immunity in the event that their experimental gene therapies proved to be ineffective or fatal.

The media constantly reminded these individuals of the deadly nature of COVID and their obligation to vaccinate for the benefit of their fellow neighbors. Threats of employment loss, education suspension, or loss of military careers compelled them to take the vaccines. President Biden even went so far as to accuse the unvaccinated of being “murderers” on national television.

Many well-intentioned individuals willingly underwent vaccinations, believing them to be “100% safe and effective.” Little did they know that Pfizer secretly possessed more than 450,000 pages clearly documenting one of the largest medical frauds and crimes against humanity ever documented.

The Power of Collective Analysis

But who had the time to analyze hundreds of thousands of pages of technical data in order to critically examine Pfizer’s claims and actions? Most journalists would not have the time to undertake such an immense task without compensation. This is where the power of collective effort came into play.

A team of 3,250 people from numerous walks of professional life came together to pour through more than 450,000 pages of the Pfizer Documents out of a love for genuine medicine and science in order to critically examine the previously secret trials of Pfizer’s experimental gene therapy. DailyClout’s COO Amy Kelly led this unpaid team, which included individuals with backgrounds in immunology, cellular biology, chemistry, statistics, biostatistics, obstetrics, cardiology, pharmacology, and many other specialties, including knowledge of government agencies and the pharmaceutical industry.

Naomi Wolf’s book, “The Pfizer Papers: Pfizer’s Crimes Against Humanity,” which publishes their findings, paints a thorough and alarming picture of the vaccine’s development, testing, and rollout.

Cardiovascular Risks

One of the most alarming findings from the Pfizer documents concerns cardiovascular risks. Compared to placebo subjects, vaccinated individuals were nearly four times more likely to die of cardiovascular events. This staggering statistic raises serious questions about the vaccine’s impact on heart health, particularly in light of the increasing reports of myocarditis and pericarditis in younger populations following vaccination.

The global vaccination campaign has left us with more questions than answers as we navigate its aftermath. The revelations from the Pfizer documents challenge us to reconsider our approach to public health crises, the role of pharmaceutical companies (and the government health organizations they help fund) in shaping health policy, and the importance of true informed consent.

This isn’t about being anti-vaccine or pro-vaccine. It’s about being pro-truth, pro-transparency, and pro-safety.

Source:

Wolf, N. & A. Kelly (2024). The Pfizer Papers: Pfizer’s Crimes Against Humanity. War Room Books.

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