Documents provided by BioNTech to the European Medicines Agency (EMA) allegedly show tens of thousands of serious adverse reactions and thousands of deaths among people who received the Pfizer-BioNTech mRNA vaccine against COVID-19 during the pandemic, when it was believed at the time that she is safe.
Documents dated August 18, 2022 and marked “confidential” show that a total of 4,964,106 adverse events were reported during clinical trials and post-vaccine release through June 18, 2022. The documents included an appendix with more detailed information on the reported adverse reactions.
Among children under the age of 17, 189 deaths and thousands of serious adverse reactions have been reported. The papers present data collected between December 19, 2021 and June 18, 2022. During this period, Pfizer-BioNTech said it found little to no safety signals and claims the vaccine has shown over 91% “effectiveness”.
Reviewing the documents, Brian Hooker, Ph.D., senior director of science and research at Child Health Defense, told the publication The Defender:
“These adverse event reports are off the charts: over 10,000 cases of myocarditis and over 9,000 cases of pericarditis. It is a crime on the part of the EMA to keep this vaccine on the market.”
According to an analysis by author Daniel Horowitz, the percentage of adverse reactions classified as serious was “well above the standard for safety signals, which typically hover around 15%,” with women reporting adverse reactions three times as often as men.
The highest number of adverse events occurred in the 31-50 age group, of which 92% had no comorbidities, making it highly likely that the vaccine caused “extensive sudden injury”. In the cumulative period, including clinical trials, the period after the launch of the vaccine and up to 18 July 2022, there were 3280 deaths among vaccine recipients.
The documents “show that Pfizer was aware of a certain painful level of side effects in the early stages” but continued to distribute its COVID-19 vaccine. These documents are not part of the ongoing court-ordered extradition of so-called “Pfizer documents” to the US, but according to Horowitz, they are pharmacovigilance documents requested by the EMA, the regulator. EU on medicines.
Pfizer-BioNTech’s flagship paper identified 9,605 adverse events (3,735 serious) and 25 cases during clinical trials in children aged 11 years and younger. Among them, 20 deaths occurred in children under the age of 5 years. The causes of these deaths included dyspnea, cardiac arrest, cardiopulmonary arrest, pyrexia, and myocarditis, although “all events were judged to be unrelated” to the vaccine.
In one of the examples given in the article, an 11-year-old boy died of acute respiratory failure two days after the first dose of the vaccine. In another case, a 6-year-old girl died seven days after the first dose of the vaccine from complications including kidney dysfunction, epilepsy, sleep apnea, seizures and “sudden death”.
For children aged 12-17 years, the document lists 21,945 adverse events (19,558 serious) in the post-marketing period and 15 cases during clinical trials. A total of 169 deaths were reported from dyspnea, pyrexia, cardiac arrest, myocarditis, heart failure, convulsions and shock.
PS I wonder when the prosecutor’s office will deal with Ms. Ursula von der Leyen’s question regarding the amounts of money that pharmaceutical companies thanked her for purchasing vaccines? After all, journalists have collected a lot of materials testifying to the selfless intentions of Madame President of the European Commission? Or is it easier to keep it under control this way?
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