News & Events | FDA - U.S. Food and Drug Administration
WEBFDA news releases, media contacts, speeches, meetings and workshops, and other ways that FDA engages with the public.
FDA Approves and Authorizes Updated mRNA COVID-19 Vaccines …
WEBAug 22, 2024 · Today, the U.S. Food and Drug Administration approved and granted emergency use authorization (EUA) for updated mRNA COVID-19 vaccines (2024-2025 formula) to include a monovalent (single)...
FDA Newsroom | FDA - U.S. Food and Drug Administration
WEBJan 4, 2023 · The latest news and events at the U.S. Food and Drug Administration (FDA) and resources for journalists.
FDA Approves Pfizer Vaccine: Live Updates - The New York Times
WEBAug 23, 2021 · President Biden lauded the final approval of the Pfizer-BioNTech vaccine by the Food and Drug Administration and implored unvaccinated Americans not to wait any longer to be inoculated.
FDA approves COVID shots from Moderna and Pfizer : Shots - Health News ...
WEBSep 11, 2023 · The Food and Drug Administration approved a new round of vaccines against COVID-19. The vaccines from Moderna and Pfizer and its partner BioNTech were approved Monday for people 12 and...
FDA approves first gene-editing treatment for human illness
WEBDec 8, 2023 · The Food and Drug Administration approved two genetic treatments for sickle cell disease, including one that uses gene-editing. The approvals offer hope for patients and signal a new...
FDA authorizes Pfizer and Moderna’s updated Covid-19 boosters
WEBAug 31, 2022 · The U.S. Food and Drug Administration has authorized a second COVID-19 booster of Pfizer-BioNTech and Moderna vaccines for people over 50 years old four months after their first booster.
F.D.A. Fully Approves Pfizer Vaccine - The New York Times
WEBAug 23, 2021 · WASHINGTON — The Food and Drug Administration on Monday granted full approval to Pfizer-BioNTech’s coronavirus vaccine for people 16 and older, a decision that is likely to set off a...
FDA expands approval of first gene therapy for rare form of ... - CNN
WEBJun 20, 2024 · The US Food and Drug Administration has given the green light for the first gene therapy that treats a rare form of muscular dystrophy to be used in most people who have the disease and a...
U.S. Food and Drug Administration Approves Bristol Myers …
WEB10 hours ago · PRINCETON, N.J.--(BUSINESS WIRE)--Bristol Myers Squibb (NYSE: BMY) today announced that the U.S. Food and Drug Administration (FDA) has approved COBENFY™ (xanomeline and trospium chloride), an ...