Pfizer Phase 3 clinical trial fraud allegations that should be immediately investigated by the FDA

Aletho News

By Steve Kirsch | June 15, 2022

There are more than a dozen “smoking guns” that indicate that the Pfizer Phase 3 trial was not properly conducted.

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For example, Dr. Peter Marks recently stated:

“We do have a problem with vaccine uptake that is very serious in the United States and anything we can do to get people more comfortable to be able to accept these potentially life-saving medical products is something that we feel we are compelled to do,” said Dr. Peter Marks, director of the Center for Biologics Evaluation and Research.

There are two things Dr. Marks can do to achieve his goal:

He can have an open discussion with the people who he alleges are the main spreaders of “misinformation.”He can open an official FDA investigation into allegations of fraud in the Pfizer trial and produce a written report responding to each allegation.

Dr. Marks, like every other public health official, will not do #1. I understand why he won’t: the data isn’t supportive of the government narrative so he’d lose the debate very badly.

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But #2 is critically important. If there is fraud/ willful misconduct, the liability protection is removed. If the FDA is truly working for the people, these allegations must be investigated.

In order to help facilitate option #2, I personally am aware of over a dozen fraud allegations that should be investigated.

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Here is only a partial list:

Pfizer admitted in a US court proceeding that there was fraud and the FDA knew about it. An admission in a court like this of fraud is surely grounds for an investigation. Watch this 2 minute video where attorney Robert Barnes describes what happened in his federal court case against Pfizer. Read this article for more: Pfizer admits to COVID vaccine clinical trial fraud in federal court.13-year old Maddie de Garay developed paralysis less than 24 hours after she was vaccinated. I know Maddie. I know her parents. Today, Maddie is confined to a wheelchair. She was perfectly healthy before she received the vaccine. Less than 24 hours after her second dose, she couldn’t walk off the school bus. Why were her symptoms reported to the FDA in the 12-15 trial results as “functional abdominal pain”? See FDA Buries Data on Seriously Injured Child in Pfizer’s Covid-19 Clinical Trial. […]There were 5 times as many exclusions in the treatment arm as in the placebo arm of the trial. It is statistically impossible for such an imbalanced number of exclusions to have happened by chance. It appears to be a deliberate culling of patients with adverse events which is not allowed.[…]Why were the allegations of data integrity documented by the BMJ never investigated by the FDA?  […] Why are there more deaths in the trial report than the document Pfizer submitted to the FDA? There were more deaths in the treatment arm than in the placebo arm. How does the FDA know for certain that the people who died in the treatment arm did not die as a result of the drug? Did they ever look at the data from Pfizer on this? If so, what convinced them the deaths were not related?
[…]A report Pfizer filed with the FDA entitled “Summary Basis for Regulatory Action” contains the following statements which are in conflict with data in the VAERS system which is reporting unprecedented increases in adverse events. There are more adverse and serious adverse events reported for the COVID vaccines than for all vaccines combined over the past 32 years. Therefore, the VAERS data and this report simply cannot both be true. The FDA needs to find out which is giving inaccurate data and correct the problem. […] Mysterious blood clots are only being found in vaccinated cadavers and have never been investigated by the CDC or FDA. Why are these blood clots only happening in vaccinated people if the vaccines are safe and effective? […]If the vaccines are safe as represented then  why does the blood of vaccinated patients look dramatically different under a darkfield microscope ?If the vaccines worked as in the trials, how can double-masked, quadruply vaccinated Tony Fauci get COVID?The Pfizer data shows  nobody became disabled, yet we had 1.8M people added to the disability system after the vaccines rolled out . If the trial data is correct, how did this happen? The trial was large enough to detect a signal this large, so how could it have gone undetected?The documents released by Pfizer show a large number of discrepancies that are impossible to explain if the trial was executed as stated. Can you investigate all the discrepancies pointed out in articles such as this and this? Brook Jackson’s whistleblower suit against Pfizer has not been dismissed  by the court.The story of patient Augusto Roux needs to be thoroughly investigated. Please see Is Subject #12312982 the Key to Proving Pfizer Vaccine Trial Fraud?Why is Sudden Adult Death Syndrome only affecting people who have been vaccinated with the COVID vaccines? Is there a counter-example?Why are athletes dying at 22X the normal rate? And why is this only happening after the vaccines rolled out?Why are there more deaths reported associated with the COVID vaccines in VAERS than for all vaccines combined in the 32 year history of the VAERS system? […].Shouldn’t the FDA and CDC call for a protective order to prevent retribution by state medical boards against physicians who are reporting adverse events and death following vaccination on social media? Clearly, the CDC and FDA are extremely safety conscious and would want to know about these incidents? So why not make a statement encouraging licensed MDs to speak out?Why are there so few autopsies? And why are the detailed autopsies showing causality ignored? And why is the CDC not warning people about the risk of death?Why is the public not permitted to see the assessments made of the 13,225 US deaths reported in the VAERS system that were determined to be not linked to the COVID vaccines? Nearly 500 articles in the peer-reviewed medical literature have been written about vaccine adverse events from the mRNA vaccines . […]Dr. John Su at the CDC appears to be a co-conspirator with Pfizer to hide the safety data. Whenever he presents, he never mentions that the VAERS data should be multiplied by the appropriate under-reporting factor (URF). This allows the vaccines to look 100 times safer than they actually are. […]Anecdotal data from physicians. There is simply too much anecdotal data from formerly pro-vax physicians who report patients who are previously healthy become “unhealthy” (new disease, existing disease reoccurs, or cognitive decline, or menstrual issues) shortly after being vaccinated.

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Via https://alethonews.com/2022/06/17/pfizer-phase-3-clinical-trial-fraud-allegations-that-should-be-immediately-investigated-by-the-fda/