Free Republic

The U.S. Food and Drug Administration (FDA) is investigating reports of relapses among people who took Pfizer’s COVID-19 pill. The FDA “is evaluating the reports of viral load rebound after completing paxlovid treatment and will share recommendations if appropriate,” an agency spokesperson told The Epoch Times in an email. In a recent preprint case report, Veterans Affairs researchers reported that a 71-year-old male who took the pill, also known as nirmatrelvir, experienced a “rapid and progressive reduction” in the viral load of SARS-CoV-2, the virus that causes COVID-19. But four days after completing the treatment course, there was a “surprising...

The Food and Drug Administration (FDA) has released the first batch of documents related to Pfizer’s COVID-19 vaccine program after a federal judge ordered that they must comply with a massive FOIA request.The request was filed by the Public Health and Medical Professionals for Transparency group, which consists of more than 30 professors and scientists. They requested any and all data that factored into the agency’s decision to authorize Phizer’s vaccine for emergency use.“The entire purpose of the FOIA is to assure government transparency,” the plaintiffs argue. “It is difficult to imagine a greater need for transparency than immediate disclosure...