Confidential documents submitted by Pfizer-BioNTech to the European Medicines Agency (EMA) strongly suggest tens of thousands of serious adverse events and thousands of deaths among people who received the Pfizer Covid-19 vaccine. This is reported by the American organization ‘Children’s Health Defense’ (CHD) in an article. For sources and references we refer to their article.
According to these documents, during the period between December 2020 and June 2022 of clinical trials and vaccine rollout, 4,964,106 adverse reactions were recorded. Among children up to 17 years of age, 189 deaths and thousands of serious side effects occurred. However, Pfizer-BioNTech saw “virtually no safety issue” during this period, claiming that the vaccine was “over 91%” effective.
Extreme
Children’s Health Defense monitors vaccination critically: “There are more than 10,000 reports of myocarditis and more than 9,000 of pericarditis. We know that this is still an underestimation of the actual numbers. It is criminal that the EMA keeps this vaccine on the market, because the rate of serious side effects is well above the safety standard of around 15%.”
Women reported three times as many side effects as men. And sixty percent of the reports concern ‘unknown outcome’ or ‘not recovered’. “This suggests that many of the side effects were permanent,” said CHD. Most adverse events occurred in the 31-50 age group, (92% with no co-morbidity, making it highly likely that the vaccine is the cause of ‘widespread sudden adverse events’. Vaccine deaths were 3,280 in According to CHD, the documents show that “Pfizer had early knowledge of an unprecedented number of side effects,” but the manufacturer continued to distribute the Covid-19 vaccine.
Thousands of serious side effects and deaths in children
“The Pfizer paper revealed 9,605 adverse events among children (3,735 of which were serious). There were 20 fatalities among children aged 5 years and older. Causes of these deaths included: shortness of breath, cardiac arrest, fever, and myocarditis. All cases were considered ‘unrelated’ to the vaccine.
One example from the document is an 11-year-old boy who died of acute respiratory arrest two days after the first dose of the vaccine. Another case reports the sudden death of a 6-year-old girl, seven days after her first dose, following complications such as renal failure, epilepsy, apnea and seizures. Another case of a 6-year-old boy is listed in the document as the cause of death of “myocarditis, cardiac and respiratory arrest and Covid-19.” He died seven days after the first dose of the vaccine.
Although the results of the autopsy were not yet known, Pfizer concluded that this boy’s death was “unrelated” to the administration of the Pfizer vaccine, and was due to “natural causes of death.”
Among children aged 12 to 17 years, the document lists 21,945 adverse events (of which 19,558 were serious) for the total period. 169 deaths were recorded, the causes of which were shortness of breath, fever, cardiac arrest, myocarditis, heart failure, seizures and shock. Nevertheless, Pfizer states that “no new significant safety risks have been identified.” ”
Pregnant women hit hard
“Pregnant and breastfeeding women were significantly affected. Among them, a total of 3,642 adverse events were seen, including: spontaneous abortion, fetal death, postpartum haemorrhage, placental detachment, premature birth, live births with congenital abnormalities, and stillbirths. Nevertheless, Pfizer saw no alarm signals in this either. However, there are two important admissions in Pfizer’s own documents: “the safety profile of the vaccine in pregnant and/or lactating women was not investigated in the clinical trial,” and “the clinical trial in mothers was terminated early due to problems with the recruitment of participants’. At the same time, Pfizer had committed to follow ‘pregnancy effects in clinical trials’.”
Pfizer identifies the knowledge gaps about vaccine use in its paper:
in pregnancy and lactation in immunocompromised patients in vulnerable patients with co-morbidities in patients with autoimmune or inflammatory diseases when interacting with other vaccines long-term safety
Incorrect numbers
“There is a striking difference between the number of reported cases of myocarditis in Pfizer’s own clinical trials and the number after, during the population rollout. There would have been only one case of myocarditis during the trial period (0.15% of all cases), while there were a total of 5,458 serious adverse events in that area (including after the roll-out). Of these, 87 cases were ‘fatal’ and 1,608 were listed as ‘not cured’. In children aged 5 to 11 years, 48 cases of myocarditis were reported (two deaths), 366 in 12-15 year olds (three deaths), 345 in 16-17 year olds and 968 in 18-24 year olds (four deaths).
An 11-year-old girl developed myocarditis two days after her first dose and subsequently died, the causes of death being myocarditis, respiratory failure, acute heart failure and respiratory arrest.
A 13-year-old boy developed myocarditis five days after his second dose and subsequently died of myocarditis, cardiac arrest, multiple organ failure, cardiac arrhythmia and renal failure.
A 13-year-old girl with no medical history developed myocarditis six days after her first dose and later died.
In a 19-year-old man, who developed myocarditis three days after his third dose and eventually died, an autopsy revealed “extensive necrosis of the left ventricle.”
And a 26-year-old man who took the flu vaccine along with the Pfizer vaccine developed myocarditis four days after his third Pfizer dose and subsequently died. The causes of death were myocarditis, arrhythmia, inflammation and left ventricular dysfunction. Autopsy results confirmed myocarditis.”
Very many serious and very rare side effects
“The 393-page confidential Pfizer document shows that Pfizer observed more than 10,000 types of conditions, many of them ‘very serious and very rare’, among a total of 73,542 people with side effects. The categories of side effects include:
vascular disorders, many of which are rare disorders of the nervous system 100 categories of eye disorders (unusual for a vaccine injury according to CHD) 47,000 ear disorders, (of which nearly 16,000 cases are tinnitus) 225,000 cases of skin and tissue disorders 190,000 cases of respiratory disorders 178,000 cases of reproductive disorders or breast disorders (including 506 cases of erectile dysfunction) 100,000 blood and lymph disorders (for which there is ample literature linking this to the spike protein) 127,000 heart disease (including rare) cardiac lesions 3,711 cases of tumors – benign and malignant 77,000 psychiatric disorders 3,092 neoplasms (malignant cancer) 68 cases of rare chronic inflammatory demyelinating polyneuropathy
“Shockingly, hundreds of very rare neurological conditions have been reported that show there is something systematically wrong with the injections,” said CHD. Despite thousands of deaths, Pfizer rarely saw a public health threat and said their vaccine was 91.3% to 100% effective. Numerous deaths and serious side effects were recorded. Including thousands of strokes resulting in hundreds of deaths, which were seen as signals but not as a possible cause by the vaccine.
A 14-year-old man died of peripheral swelling after receiving the Covid-19 vaccine, with no additional details.
A 67-year-old man “with a history of diabetes and an autoimmune platelet disorder” developed chest and gastrointestinal pain within 30 minutes of his third dose of vaccine. A diagnosis of anaphylaxis was made, while an electrocardiogram showed ‘signs of myocardial infarction’. He later went into cardiac arrest and died 12 days after his vaccination.”
Alarm signals
“There was one alarm signal: hearing loss, after which the pharmaceutical company promised to carry out a ‘safety check of tinnitus and hearing loss’. Myocarditis and pericarditis were identified as a ‘major risk’, while irritability was identified as a negligible risk. Despite the large number of deaths and serious adverse events, Pfizer wrote that “…no modifications or additional risk reductions are necessary…”
The EMA seems to agree with Pfizer’s conclusions. In their report, their Risk Assessment Committee (PRAC) wrote that ‘the risk-benefit ratio (…) remains unchanged (…) thus recommending that the marketing authorisation(s) be maintained’.
CHD calls the number of deaths and injuries following the vaccines “sickening,” and condemns Pfizer and the EMA for rolling out the Covid-19 vaccine.
Earlier this month, BioNTech was sued in Germany with a demand of at least 150,000 euros in compensation for physical injury and compensation for material damage.”
From Pfizer- BioNTech documents were originally requested by the EMA, the European medicines watchdog. And came out through an Austrian WOO request. However, no mainstream media outlet has reported on it; the existence of the documents only became known when independent English-language bloggers discovered and published the documents.
2023-07-16 20:18:07
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