A set of confidential documents showing data from Pfizer-BioNTech’s vaccination in Europe, recorded between December 19, 2021 and June 18, 2022, detailing tens of thousands of adverse events and deaths that occurred among the people that have been vaccinated during the clinical trials and during the post-marketing period, which began in December 2020 up until June 18, 2022.
Despite these findings from the EU reports, Pfizer-BioNTech still gave no “almost no safety signals” while also claiming that “the vaccine demonstrated over 91% efficacy.” The said documents released by Pfizer-BioNTech to the European Medicines Agency (EMA), dated Aug. 18, 2022, have shown a total of 4,964,106 recorded adverse events. It also includes other important details such as an appendix about the identified adverse events.
According to the document, there were about 3,280 fatalities among those who received the jab all in all in the period until July 18, 2022. Sixty percent of cases were reported with either “outcome unknown” or “not recovered”. Therefore, the documents suggest that the injuries are not temporary but instead, serious and disturbing. As reported by the Defender / Children’s Health Defense (CHD):
“The highest number of cases occurred in the 31-50 age group, of which 92% did not have any comorbidities, making it very likely it was the vaccine causing “such widespread, sudden injury.
Among children under age 17, 189 deaths and thousands of serious adverse events were reported.”
The document, which is not part of the famous so-called “Pfizer documents” obtained by courts, also demonstrates that myocarditis and pericarditis are very common occurrences, with over 10,000 for the former and over 9,000 for the latter. Within this context, women are three times higher to get the chance compared to men. Even though it is a criminal act against your own government if you keep these ineffective and unsafe vaccines running on the market, the EMA seems still in bed with Pfizer-BioNTech, doing the dirty job.
Obviously, the documents suggest that Pfizer-BioNTech are aware of the disheartening facts about the reported adverse events and injuries yet show no concern whatsoever. Despite this knowledge, the big pharma giants continue to distribute the vaccines not only in the EU regions but also to other parts of the world. As CHD reported recently:
“The main Pfizer-BioNTech document revealed 9,605 adverse events (3,735 serious) during the PSUR #3 and 25 cases during the clinical trials among children ages 11 and younger. These included 20 fatalities, in children as young as 5 years old.
Causes of these fatalities included dyspnea, cardiac arrest, cardio-respiratory arrest, pyrexia and myocarditis, though “all events were assessed as unrelated” to the vaccine.”
There were 21, 945 adverse events reported for children with the ages of 12-17, and 19,558 of these are serious, including 15 cases during clinical trials. Totaling up to 169 deaths, the recorded causes include “dyspnea, pyrexia, cardiac arrest, myocarditis, cardiac failure, seizure and shock”. In the listed deaths of children and young adults from myocarditis and pericarditis, the CHD reported:
“A notable discrepancy appears in terms of reported cases of myocarditis in the clinical trials as compared to the post-marketing period — one myocarditis case (0.15% of all cases) is listed for the clinical trial period, while 5,422 cases (1.1% of all cases) and 5,458 serious events were reported in the PSUR #3 period.
Of these, 87 cases were fatal and 1,608 were listed as “not resolved.” Among children and young adults, 48 cases were reported for those between the ages of 5 and 11 (two deaths), 366 among 12-15-year-olds (three deaths), 345 among 16-17-year-olds and 968 among 18-24-year-olds (four deaths).”
To read/download the full Pfizer-BioNTech report, go to this link:
Featured image: https://www.eutimes.net/2023/06/confidential-eu-documents-reveal-thousands-of-deaths-from-pfizer-biontech-covid-jabs/