When considering a drug for emergency use authorization (EUA), the Food and Drug Administration (FDA) selects an internal advisory committee to review information and data submitted to the FDA by the pharmaceutical company about its new drug. These influential FDA advisory committees, based on that information and data, make recommendations […]
Report 95: mRNA COVID-19 Shots – ‘Vaccines’ or Gene Therapy Products? – Part 1
To this day — more than three years after Pfizer and Moderna’s mRNA COVID-19 drugs received Emergency Use Authorization (EUA) —Â television, radio, and the Internet still inundate the public with ads, messages, and stories about COVID vaccines. But, are the mRNA COVID-19 shots genuinely vaccines? These products never aligned […]