The documentation, which was handed over to the European Medicines Agency (EMA) last year, the European equivalent of the Food and Drug Administration (FDA), contains damning information showing that Fauci Flu shots are anything but "safe and effective" as publicly claimed.
Just like what happens in the United States, the European public was never informed about these very serious safety signals, which the EMA apparently did not even know about until somewhat recently.
Dated Aug. 18, 2022, and marked "confidential," the documents show that cumulatively during the clinical trials and post-marketing period between Dec. 19,2021, and June 18, 2022, known as the "PSUR #3 period," a total of 4,964,106 adverse events were recorded. An appendix was also included outlining further specifics about these adverse events.
In children under the age of 18, there were thousands of serious adverse events and 189 recorded deaths. None of this was made public, meaning parents who signed their children up for mRNA injections at the recommendation or order of the government had no idea their children could become seriously disabled or die from the shots.
(Related: Did you catch Report 71 from the Pfizer documents showing horrific drug industry crimes against humanity?)
The documents include data collected between Dec. 19, 2021, and June 18, 2022, known as the "PSUR #3 period." They also include cumulative data on adverse events and deaths that occurred during clinical trials and all throughout the post-marketing period beginning in December 2020 when then-President Trump launched Operation Warp Speed.
At the time when Pfizer-BioNTech submitted these documents to the EMA, it was still claiming that there were no safety signals and that its mRNA shots have an over 91 percent "efficacy" rate.
"These adverse event reports are 'off the charts,' with myocarditis reports at over 10,000 and pericarditis reports at over 9,000," commented Brian Hooker, PhD, PE, senior director of science and research for Children's Health Defense (CHD) about the revelations.
"Historically, we know that this would be an under-ascertainment of the actual numbers. It is criminal for the EMA to keep this vaccine on the market."
Commentator and author Daniel Horowitz also chimed in that, according to his own analysis, the percentage of adverse events classified as serious is "well above the standard for safety signals usually pegged at 15 percent."
We know that women reported adverse events at three times the rate of men. Sixty percent of cases were reported with either "outcome unknown" or "not recovered," suggesting that many of the injuries "were not transient," according to Horowitz.
Up to July 18, 2022, there were 3,280 fatalities recorded among jab recipients, a shocking figure in light of the false claims made by Pfizer-BioNTech, the rest of the drug industry, and the government about their alleged safety and effectiveness.
Horowitz added that these documents "show that Pfizer knew about a sickening level of injury early on," and yet continued to distribute the injections all around the world to unsuspecting victims.
While not part of the court-ordered release of the so-called "Pfizer documents," these "confidential" documents are part of a pharmacovigilance documents request made by the EMA.
Stemming from "a FOIA (Freedom of Information Act) request from an anonymous reader," the documents were procured to an Austrian scientist and politics blog called TKP. They were subsequently published on March 4.
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