mRNA Vaccines and EUA

 Emergency Use Authorization

• All of the mRNA vaccine doses administered in the United States have been provided under "Emergency Use Authorization" (EUA), which is to say that although the FDA has licensed the Pfizer/Bio-N-Tech and Moderna vaccines for some age cohorts, the firms have elected to not manufacture, distribute, or market these licensed products in the US States.
• EUA is a preferred pathway for marketing their products. A single purchaser (the US Government) provides complete liability indemnification, a guaranteed market with very little oversight.

Implications

• The extensive random incorporation of pseudouridine into the synthetic mRNA-like molecules used for the Pfizer/BioNTech and Moderna SARS-CoV-2 vaccines may well account for much or all of the observed immunosuppression, DNA virus reactivation, and remarkable persistence of the synthetic "mRNA" molecules observed in lymph node biopsy tissues.
• Pseudouridine likely affects multiple facets of mRNA function.

https://rwmalonemd.substack.com/p/mrna-vaccines-and-eua?utm_source=post-email-title&publication_id=583200&post_id=80795186&isFreemail=true&utm_medium=email