August 3, 2023, the Australian Senate Education and Employment Committee1 held a COVID hearing in which Sen. Gerard Rennick asked Dr. Krishan Thiru, Pfizer’s Australian medical director, to explain the mechanism of how the mRNA COVID shot causes myocarditis.2 Thiru, however, kept talking in circles rather than answering the question. Rennick valiantly tried, without success,… Read More »
The U.S. Food and Drug Administration and the Centers for Disease Control and Prevention jointly run and, allegedly, monitor the Vaccine Adverse Events Reporting System (VAERS) for safety signals. Both agencies have been blatantly derelict in their duties in this regard, as the safety signals in VAERS have been screaming for attention since the first… Read More »
Despite the FDA’s claim that it is committed to transparency, especially for COVID-19 emergency use authorizations (EUAs),1 the agency first requested 55 years to release the data supporting the approval of Comirnaty after a Freedom of Information Act (FOIA) request was filed,2 and then asked for an extra 20 years to fully comply.3 Pfizer has… Read More »