- In November 2021, Brook Jackson, a whistleblower who worked on Pfizer’s Phase 3 COVID jab trial in the fall of 2020, warned she’d seen evidence of fraud in the trial
- With the release of Pfizer trial data — which they tried to withhold for 75 years — additional problems suggestive of fraud and data manipulation are coming to light
- Trial site 1231, located in Argentina, somehow managed to recruit 10% of the total trial participants, 4,501 in all, and they did so in just three weeks, and without a contract research organization — a feat that has many questioning whether fraud was committed
- The lead investigator for trial site 1231 is Dr. Fernando Polack, who also happens to be a consultant for the U.S. Food and Drug Administration’s Vaccines and Related Biological Products Advisory Committee (RBPAC), a current adjunct professor at Vanderbilt University in Tennessee, an investigator for Fundación Infant, funded by the Bill & Melinda Gates foundation, and the first author of Pfizer’s paper, “Safety and Efficacy of the BNT162b2 mRNA COVID-19 Vaccine,” published at the end of December 2021
- Site 1231 held a second enrollment session, given the designation of “site 4444.” The 4444 trial site data raise another red flag. It supposedly enrolled 1,275 patients in a single week, from September 22 through 27, 2020 — the last week that recruitment could take place to meet the data cutoff for the FDA meeting in December 2020. Was “site 4444” fabricating data to create the appearance that the jab was having an effect?
"Revelations of poor practices at a contract research company helping to carry out Pfizer's pivotal COVID-19 vaccine trial raise questions about data integrity and regulatory oversight ...
[F]or researchers who were testing Pfizer's vaccine at several sites in Texas during that autumn, speed may have come at the cost of data integrity and patient safety ... Staff who conducted quality control checks were overwhelmed by the volume of problems they were finding."Jackson, a former regional director of Ventavia Research Group, a research organization charged with testing Pfizer's COVID jab at several sites in Texas, repeatedly "informed her superiors of poor laboratory management, patient safety concerns and data integrity issues," Thacker wrote.
When her concerns were ignored, she finally called the U.S. Food and Drug Administration and filed a complaint via email. Jackson was fired later that day after just two weeks on the job. According to her separation letter, management decided she was "not a good fit" for the company after all.
BMJ Report CensoredDisturbingly, social media actually censored this BMJ article and published pure falsehoods in an effort to "debunk" it. Mind you, the BMJ is one of the oldest and most respected peer-reviewed medical journals in the world! The Facebook "fact check" was done by Lead Stories, a Facebook contractor, which claimed the BMJ "did NOT reveal disqualifying and ignored reports of flaws in Pfizer's" trials.2
- Inaccurately referred to The BMJ as a "news blog"
- Failed to specify any assertions of fact that The BMJ article got wrong
- Published the fact check on the Lead Stories' website under a URL that contains the phrase "hoax-alert"
Pfizer Trial Data Raises Suspicions of FraudNow, with the release of Pfizer trial data8 — which they tried to withhold for 75 years — internet sleuths are finding additional problems suggestive of fraud and data manipulation. May 9, 2022, a Twitter user named Jikkyleaks posted a series of tweets questioning data from Pfizer trial sites 1231 and 4444.9
- A consultant for the U.S. Food and Drug Administration's Vaccines and Related Biological Products Advisory Committee (RBPAC) since 2017
- A current adjunct professor at Vanderbilt University in Tennessee
- An investigator for Fundación Infant,12 which is funded by the Bill & Melinda Gates foundation13
- The first author of Pfizer's paper,14 "Safety and Efficacy of the BNT162b2 mRNA COVID-19 Vaccine," published at the end of December 2021
This recruitment also took place seven days a week, which is another red flag. "Weekend recruitment for a clinical trial would be odd. Staff are needed to fill out that many record forms (CRFs) and there are potential risks to the trial, so you need medical staff. It would be highly unusual," Jikkyleaks notes.
Questions Surround Site 4444 DataNow, "site 4444" does not exist. It's actually the same as site 1231. It appears site 1231 held a second enrollment session, and these were for some reason given the designation of 4444. The 4444 trial site data raise another red flag.
"My guess: they needed enough numbers of 'positive PCR tests' in the placebo group to show a difference between groups for that VRBPAC meeting on the 10th Dec, and they didn't have them. So, site 4444 appeared and gave them their 'perfect' result. Bravo."
"Was there fraud in the Pfizer trial? Without a doubt. The story of Maddie de Garay is a clear case of that. Brook Jackson has evidence of fraud; she has 17 lawyers working for her. If there wasn't fraud, these lawyers wouldn't be wasting their time.
This new data on Site 1231/4444 looks suspicious to me. It looks too good to be true. But we can't make the call without more information. Undoubtedly, the mainstream media will not look into this, Pfizer will remain silent, and Polack will be unreachable for comment. The lack of transparency should be troubling to everyone. That is the one thing we can say for sure."
Pfizer Documents Reveal COVID Jab Dangers
In the video, Campbell reviews the documents listed as "5.3.6. Postmarketing Experience," which were originally marked "confidential." They reveal that, cumulatively, through February 28, 2021, Pfizer received 42,086 adverse event reports, including 1,223 deaths.
To have 1,223 fatalities and 42,086 reports of injury in the first three months is a significant safety signal, especially when you consider that the 1976 swine flu vaccine was pulled after only 25 deaths.
158,000 Recorded Side Effects — A World Record?The first really large tranche of more than 10,000 Pfizer documents was released March 1, 2022. (You can find them all on PHMPT.org.19) In this batch were no less than nine single-space pages of "adverse events of special interest," listed in alphabetical order20 — 158,000 in all!
CRF Anomalies Raise Questions of FraudAfter reviewing some of the released CRFs in the March 1 tranche, investigative journalist Sonia Elijah also discovered several problems, including the following:23
- Patients entered into the "healthy population" group who were far from healthy — For example, one such "healthy" participant was a Type 2 diabetic with angina, a cardiac stent and a history of heart attack.
- Serious adverse event (SAE) numbers were left blank — Ventavia site No. 1085 has a particularly large number of missing SAE numbers.
- Missing barcodes for samples collected — Without those barcodes, you can't match the sample to the participant.
- Suspicious-looking SAE start and end dates — For example, the so-called "healthy" diabetic suffered a "serious" heart attack October 27, 2020. The "end" date is listed as October 28, the next day, which is odd because it was recorded as serious enough to require hospitalization.
- Unblinded teams were responsible for reviewing adverse event reports for signs of COVID cases, and to review severe COVID cases — Yet in some cases they appear to have dismissed the possibility of an event being COVID-related, such as pneumonia. This despite the fact that Pfizer's protocol (section 8.2.4) lists "enhanced COVID-19" (i.e., antibody dependent enhancement) as a potential side effect to be on the lookout for. As noted by Elijah:
"Inadvertently, this could have led to bias, as the unblinded teams would have been aware which participants were assigned the placebo and those who received the vaccine. They might have been under pressure by the sponsor for the trial to go a certain way and for events like 'COVID Pneumonia' to be classified simply as pneumonia."
- Impossible dating — The diabetic who suffered a heart attack followed by pneumonia (which may have been unacknowledged COVID pneumonia) died, and the date of death is listed as the day before the patient supposedly went for a "COVID ill" visit.
- Second dose administered outside the three-week protocol window.
- Observation period appears to have been an automatic entry — According to the protocol, each participant was to be observed by staff for a minimum of 30 minutes.
- Adverse events listed as "not serious" despite extended hospital stay — In one case, the participant fell and suffered facial lacerations the day after the second dose and was hospitalized for 26 days, yet the fall was not reported as serious.
Elijah writes, "Doubts can be raised over the credibility of this information given the fall and facial lacerations were intrinsically related. So, if facial lacerations were due to 'hypotension' then the fall should be due to that too." Might low blood pressure be an effect of the experimental shot? Possibly. Especially when you consider the patient fell the day after being given the second dose.
- Dismissing brand new health problems as unrelated to the treatment — For example, in one case, a female participant with no medical history of impaired kidney function was diagnosed with kidney stones and severe hypokalemia, requiring hospitalization, one month after her second dose. Yet despite her having no history of kidney problems, both events were dismissed as "not related" to the study treatment and no further investigation was done.
"All the evidence gleaned over a limited time appears to back up whistleblower Jackson's claims of poor trial site data management and raises questions as to how Ventavia conducted the Pfizer clinical trials.
The errors and anomalies in the CRFs also allude to her claims that the clinical research associates were not trained adequately, with many having had no prior clinical experience history. If such egregious findings are true at these sites, could they manifest at other trial sites around North America and beyond?"
Can You Trust Pfizer?Pfizer, which was quickly given emergency use authorization (EUA) for its COVID-19 mRNA gene therapy shot, has a long list of criminal verdicts against it:
Despite its tarnished history, we're now expected to trust that everything Pfizer does is above-board. I don't think so. A company that continues getting caught committing the same crimes over and over again clearly has a deeply established ethical rot within its corporate structure that fines simply have no effect over.Has Pfizer committed fraud in its COVID jab trials as well? It sure looks that way. Time will tell whether attorneys will have enough for a conviction in the future. If fraud did take place, Pfizer can (and likely will) be held liable for the more than one million injuries its injection has caused in the U.S. alone, and we all look forward to that reckoning.
Sources and References
- 1 The BMJ 2021; 375:n2635
- 2, 3 Reclaim the Net December 17, 2021
- 4 Medscape December 20, 2021
- 5 ZeroHedge December 20, 2021
- 6, 7 The BMJ 2021;375:n2635
- 8 Icandecide.org Released Pfizer Data
- 9, 11, 16 Twitter Jikkyleaks May 9, 2022
- 10 DavidHealy.org March 24, 2022
- 12 Infant.org.ar
- 13 Gates Foundation Fundacion Infant
- 14 NEJM 2020; 383: 2603-2615
- 15, 17 Steve Kirsch Substack May 9, 2022
- 18 Steve Kirsch Substack March 11, 2022
- 19 PHMPT.org Pfizer Documents
- 20 Peckford42 Wordpress March 3, 2022
- 21 Applied Clinical Genetics 2015; 8: 189-200
- 22 Medicinenet.com 1p36 Deletion Syndrome
- 23, 24 Trial Site News March 7, 2022
- 25, 26, 27, 29, 31 Healthcare Policy May 2010; 5(4): 16-25
- 28 U.S. Department of Justice September 2, 2009
- 30 U.S. Department of Justice May 24, 2018