Posted on 02/11/2024 2:26:20 AM PST by RandFan
Abstract
Our understanding of COVID-19 vaccinations and their impact on health and mortality has evolved substantially since the first vaccine rollouts. Published reports from the original randomized phase 3 trials concluded that the COVID-19 mRNA vaccines could greatly reduce COVID-19 symptoms. In the interim, problems with the methods, execution, and reporting of these pivotal trials have emerged. Re-analysis of the Pfizer trial data identified statistically significant increases in serious adverse events (SAEs) in the vaccine group. Numerous SAEs were identified following the Emergency Use Authorization (EUA), including death, cancer, cardiac events, and various autoimmune, hematological, reproductive, and neurological disorders. Furthermore, these products never underwent adequate safety and toxicological testing in accordance with previously established scientific standards. Among the other major topics addressed in this narrative review are the published analyses of serious harms to humans, quality control issues and process-related impurities, mechanisms underlying adverse events (AEs), the immunologic basis for vaccine inefficacy, and concerning mortality trends based on the registrational trial data. The risk-benefit imbalance substantiated by the evidence to date contraindicates further booster injections and suggests that, at a minimum, the mRNA injections should be removed from the childhood immunization program until proper safety and toxicological studies are conducted. Federal agency approval of the COVID-19 mRNA vaccines on a blanket-coverage population-wide basis had no support from an honest assessment of all relevant registrational data and commensurate consideration of risks versus benefits. Given the extensive, well-documented SAEs and unacceptably high harm-to-reward ratio, we urge governments to endorse a global moratorium on the modified mRNA products until all relevant questions pertaining to causality, residual DNA, and aberrant protein production are answered.
(Excerpt) Read more at pubmed.ncbi.nlm.nih.gov ...
My where could she be?? Where oh where? I would think if you possessed the biological wisdom of the universe and got to wear cool space suits to design the down fall of man in a lab you would have some amazing comment here. Alas lies and arrogance can only take you so far. I am sure when she graces us with her unbelievable wisdom she will tell us these are all lies, bats caused it all and Pfizer is gods gift of grace to us all.
no they wanted the profits, and big pharma has a big lobbying group based in DC.
“During the course of the experiment, the scientist in charge must be prepared to terminate the experiment at any stage, if he has probable cause to believe in the exercise of good faith, superior skilll and careful judgment required by him that a continuation of the experiment is likely to result in injury, disability, or death to the experimental subject.”
Nuremberg Code
VAERS
Ma$$ Murderers have indemnification?
Another bump for your link. Thanks again, mewzilla.
BUMP link.
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