by Robert W. Malone M.D., M.S., Childrens Health Defense:
The Journal of Insulin Resistance published a two-part research paper, “Curing the pandemic of misinformation on COVID-19 mRNA vaccines through real evidence-based medicine.”
This was written by one of the U.K.’s most eminent cardiologists, Dr. Aseem Malhotra, who was one of the first to take two doses of the vaccine and promote it on “Good Morning Britain.”
Malhotra now says that since the rollout of the vaccine, the evidence of its effectiveness and true rates of adverse events have changed and now, “There is a strong scientific, ethical, and moral case to be made that COVID-19 vaccines rollout must stop immediately until raw data has been released for fully independent scrutiny.”
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Furthermore, real-world data reveal that in the non-elderly population, the number needed to vaccinate to prevent one death from COVID-19 runs into thousands and that re-analysis of randomized controlled trial data from the initial vaccine clinical trials suggests a greater risk of suffering a serious adverse event from the vaccine than to be hospitalized with COVID-19.
Summary overviews of the two-part research paper are below, together with a transcript of the above video in which he introduces his findings.
“Background: In response to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), several new pharmaceutical agents have been administered to billions of people worldwide, including the young and healthy at little risk from the virus.
“Considerable leeway has been afforded in terms of the pre-clinical and clinical testing of these agents, despite an entirely novel mechanism of action and concerning biodistribution characteristics.
“Aim: To gain a better understanding of the true benefits and potential harms of the messenger ribonucleic acid (mRNA) coronavirus disease (COVID) vaccines.
“Methods: A narrative review of the evidence from randomised trials and real world data of the COVID mRNA products with special emphasis on BionTech/Pfizer vaccine.
“Results: In the non-elderly population the ‘number needed to treat’ to prevent a single death runs into the thousands.
“Re-analysis of randomised controlled trials using the messenger ribonucleic acid (mRNA) technology suggests a greater risk of serious adverse events from the vaccines than being hospitalised from COVID-19s.
“Pharmacovigilance systems and real-world safety data, coupled with plausible mechanisms of harm, are deeply concerning, especially in relation to cardiovascular safety.
“Mirroring a potential signal from the Pfizer Phase 3 trial, a significant rise in cardiac arrest calls to ambulances in England was seen in 2021, with similar data emerging from Israel in the 16–39-year-old age group.
“Conclusion: It cannot be said that the consent to receive these agents was fully informed, as is required ethically and legally. A pause and reappraisal of global vaccination policies for COVID-19 is long overdue.”
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