The coronavirus vaccine became available in December 2020, and although it is not often mentioned in the major media, you can find out how many people have been affected by side effects since then. Confidential documents have just recently been revealed that Pfizer Pharmaceuticals knew about the drastic increase in adverse reactions to its Covid mRNA vaccine.
It is Pfizer’s pharmacovigilance documents requested by the European Union’s drug regulator, the European Medicines Agency. During the period when vaccine makers were claiming “no symptoms were seen,” Pfizer was aware of tens of thousands of serious adverse events and thousands of deaths among people who received its mRNA novel coronavirus vaccine. A document marked “confidential” dated August 18, 2022 indicated that a cumulative total of 4,964,106 adverse events were recorded during the clinical trials and post-marketing period through June 18, 2022, and included an appendix detailing the adverse events identified.
Also in January 2023, Peter Dorsey, editor of the British Medical Journal, along with other experts (current and former advisors to the U.S. Food and Drug Administration (FDA), as well as professional scholars), requested that the FDA update its product labeling to reflect the reality of what we have learned about the novel coronavirus vaccine. In particular, they asked to label side effects such as pediatric multisystem inflammatory syndrome, pulmonary embolism, sudden cardiac death, neuropathy and autonomic neuropathy, decreased sperm concentration, heavy menstrual bleeding, and detection of vaccine mRNA in breast milk, but the FDA denied almost all of their requests.
Peter Dorci commented, “Product labeling should be informative and accurate, not promotional. The law mandates it, and compliance with the law should not be optional.” I hope you all recognize that this is the attitude of a national institution that should be protecting us.
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