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by ICAN at ICAN Decide
Pfizer’s own informed consent documents, recently obtained by ICAN, show it discloses potential concerns, including myocarditis, original antigenic sin, and birth defects, while the FDA & CDC whitewash these concerns to declare these products are safe and effective.
ICAN has now obtained the materials used by the Cincinnati’s Children’s Hospital in conducting its studies of the Pfizer booster vaccine, including in children. The documents prepared in consultation with Pfizer tell us a lot about how Pfizer understands the risks of its products.
Pfizer is clearly worried about the risks of myocarditis (heart inflammation) in kids. Pfizer’s own informed consent documents reveal that the risk of myocarditis may be as high as 1 in 1,000 (see page 4).
But the FDA and CDC blithely ignored this risk in approving the Pfizer mRNA shot in kids. Only after rushing this product through the approval process did the CDC begrudgingly admit that “Myocarditis and pericarditis have rarely been reported, especially in adolescents and young adult males within several days after COVID-19 vaccination.”
Pfizer is also aware of the possibility of original antigenic sin and pathogenic priming (unwanted immune responses that leave one worse off in response to a virus than if one had done nothing). Pfizer warns parents of clinical trial participants that “it cannot yet be ruled out that the study vaccine could make a later COVID-19 illness more severe” (emphasis added). The FDA and CDC go to great lengths to hide that information while proclaiming “safe and effective” over and over again like a mantra.
Pfizer appears very worried about the potential of the teratogenesis (harm to a developing fetus) and even possibly mutagenesis (harm to DNA). So even though this is a trial in children, Pfizer disclosed to the parents of these children that “the effects of the COVID-19 vaccine on sperm, a pregnancy, a fetus, or a nursing child are not known.”
But then Pfizer goes even further to state that:…
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