{"id":6524,"date":"2024-12-02T06:44:47","date_gmt":"2024-12-02T11:44:47","guid":{"rendered":"https:\/\/stateofthenation.info\/?p=6524"},"modified":"2024-12-02T06:44:47","modified_gmt":"2024-12-02T11:44:47","slug":"breaking-new-study-demands-immediate-moratorium-on-covid-19-mrna-injections","status":"publish","type":"post","link":"https:\/\/stateofthenation.info\/?p=6524","title":{"rendered":"

BREAKING – New Study Demands Immediate Moratorium on COVID-19 mRNA Injections<\/b>

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READ HERE:<\/a><\/strong><\/p>\n

Pfizer\/BioNTech\u2019s COVID-19 modRNA Vaccines: Dangerous Genetic Mechanism of Action Released before Sufficient Preclinical Testing<\/h3>\n

By Nicolas Hulscher, MPH<\/p>\n

As calls for an immediate moratorium<\/a> on COVID-19 mRNA injections intensify\u2026<\/p>\n

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\u2026Oldfield et al just published a new study in the Journal of American Physicians and Surgeons<\/em> titled, Pfizer\/BioNTech\u2019s COVID-19 modRNA Vaccines: Dangerous Genetic Mechanism of Action Released before Sufficient Preclinical Testing<\/a>:<\/strong><\/p>\n

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Here\u2019s a concise summary of the study\u2019s main points: <\/strong><\/p>\n

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  1. Regulatory Classification and Guidelines<\/strong>:\n
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    • COVID-19 modRNA vaccines were misclassified as traditional vaccines rather than gene therapy products, bypassing stricter regulatory requirements.<\/li>\n
    • WHO guidelines from 2005 were used for nonclinical assessments, despite being outdated and inapplicable to modRNA vaccines.<\/li>\n<\/ul>\n<\/li>\n
    • Spike Protein and Safety Concerns<\/strong>:\n
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      • The spike protein produced by modRNA vaccines is toxic and can cause immune-related complications.<\/li>\n
      • Studies on pharmacokinetics (how much spike protein is produced, where it distributes, and how long it persists) were not conducted as part of Pfizer\u2019s submission.<\/li>\n
      • Spike protein production varies among individuals based on genetics, health status, and other factors, but this variability was never studied.<\/li>\n<\/ul>\n<\/li>\n
      • Biodistribution and LNP Behavior<\/strong>:\n
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        • Pfizer\u2019s own biodistribution data showed lipid nanoparticles (LNPs) and modRNA were widely distributed throughout the body, including the liver, spleen, ovaries, and adrenal glands.<\/li>\n
        • Contrary to claims, spike protein production was not limited to the injection site, raising concerns about off-target effects and toxicity.<\/li>\n<\/ul>\n<\/li>\n
        • Toxicology and Carcinogenicity Testing<\/strong>:\n
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          • Pfizer did not conduct genotoxicity or carcinogenicity studies, despite the potential for the spike protein and LNPs to cause harm.<\/li>\n
          • Wistar Han\u2122 rats, which are not a relevant species for SARS-CoV-2 toxicity studies, were used inappropriately in preclinical testing.<\/li>\n<\/ul>\n<\/li>\n
          • Deficient Clinical Trials<\/strong>:\n
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            • Phase I clinical trials failed to measure critical factors like the amount and variability of spike protein produced in individuals.<\/li>\n
            • Placebo groups in initial trials were unblinded early, undermining the integrity of long-term safety and efficacy data.<\/li>\n<\/ul>\n<\/li>\n
            • Adverse Events and VAERS Reporting<\/strong>:\n
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              • Post-authorization data from Pfizer showed 1,223 deaths and numerous serious adverse events within the first three months of vaccine rollout.<\/li>\n
              • The Vaccine Adverse Event Reporting System (VAERS) documented a huge spike in reported adverse events following the COVID-19 vaccine rollout, far exceeding reports for previous vaccines.<\/li>\n
              • Despite the massive increase in reported deaths and injuries, no corrective actions were taken. This contrasts with earlier vaccines like Rotashield\u00ae, which were removed after only 15 cases of intussusception:<\/li>\n<\/ul>\n
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                1. Regulatory Oversight Failures<\/strong>:\n
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                  • The FDA and other global regulatory agencies overlooked or dismissed major concerns raised during the review process.<\/li>\n
                  • Regulatory assessments relied on insufficient data and assumptions rather than rigorous scientific evidence.<\/li>\n<\/ul>\n<\/li>\n
                  • Call for a Moratorium<\/strong>:\n
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                    • Based on incomplete data, serious safety concerns, and potential long-term risks, the authors recommend a moratorium on Pfizer\/BioNTech\u2019s COVID-19 modRNA vaccines.<\/li>\n
                    • Proper studies must be conducted to ensure safety, as the responsibility lies with the pharmaceutical industry, not independent scientists.<\/li>\n<\/ul>\n<\/li>\n<\/ol>\n

                      Since the proper conditions for market withdrawal have been met, the primary obstacle preventing an immediate moratorium on COVID-19 genetic injections is our captured regulatory agencies, which will hopefully be dealt with after the Senate confirmation process.<\/p>\n

                      Nicolas Hulscher, MPH<\/strong><\/p>\n

                      Epidemiologist and Foundation Administrator, McCullough Foundation<\/p>\n

                      www.mcculloughfnd.org<\/p>\n

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