The U.S. Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC) routinely violate their own standards and the fundamental norms of science when reviewing Emergency Use Authorizations (EUA) and Biologics License Applications from pharmaceutical companies that wish to introduce a new vaccine. The FDA publishes a 242-page book called Communicating Risk … Continue reading Pfizer Covid ‘Vaccine’ FAILS Risk-Benefit Analysis in Children 5 to 11