Just hours after Pfizer and its partner BioNTech announced their plan to seek federal authorization to market a "booster" jab that they said would provide better protection against COVID variants like Delta, the FDA and CDC issued a joint statement c
FDA pushing to mandate "supplement registration" scheme while completely ignoring the 50,000+ Americans injured each year by over-the-counter pharmaceuticals
People are seen walking the promenade at Bondi Beach on Saturday morning. Picture: NCA NewsWire/Bianca De MarchiSource: News Corp Australia
Dr. Anthony Fauci, director of the U.S. National Institute of Allergy and Infectious Diseases, favors using remdesivir, despite a lack of science-based evidence of it being effective against COVID-19
The FDA now states that "results from SARS-CoV-2 antibody tests should not be used to evaluate immunity or protection from COVID-19 at any time, and especially after the person received a COVID-19 vaccination," after using the tests on many peopl
Pfizer Inc and its German partner BioNTech SE plan to ask for FDA emergency use authorization of its COVID-19 vaccine in children under age 12 by fall
Audience: Individuals Performing COVID-19 Testing Level: Laboratory Alert
--turning blind eye to safety signals Since the mid-1980s, the number of childhood shots on the Centers for Disease Control and Prevention (CDC) vaccine schedule has more than quadrupled.
Authorities say no change in vaccine policy but risks should be disclosed
During the recent America's Frontline Doctors speaking tour in Tennessee, Dr Simone Gold, an LA-based physician with a law degree from Stanford joins self-described "hillbilly" broadcasters, Tim Greer and Brad Barton to talk about the experimen
The Food and Drug and Administration (FDA) is forcing Johnson & Johnson to throw out millions of doses of its single-shot COVID-19 vaccine produced at a troubled plant in Baltimore due to contamination concerns.
Josh Sigurdson reports on mounting evidence of vaccine injuries and deaths as the CDC calls an emergency meeting and the FDA demands Johnson & Johnson to destroy 60 million doses.
The US Food and Drug Administration (FDA) has approved a new weight management drug called Wegovy (semaglutide). The drug was first approved as a type 2 diabetes treatment in 2017 and has subsequently been described as a "game-changer" for obese
Update (1339ET): And just like that, Biogen shares have already been halted again due to volatility. BIOGEN HALTED FOR VOLATILITY But not before Biogen's torrid rally helped carry the Nasdaq Biotech Index to a 5.5% rally on the day, its biggest int
The numbers shown by the trial were more than alarming. Even though 86% of the children suffered side effects after the first dose, the researchers continued experimenting and injected them with a second RNA vaccine.