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FDA Approves Skyrizi for Ulcerative Colitis
Medscape· 1 day agoThe approval is the fourth indication for the anti–interleukin 23 monoclonal antibody after approval for Crohn's disease, psoriatic arthritis, and plaque...
Aurion Biotech gets FDA approval to speed development of vision restoring treatment
GeekWire· 11 hours agoFood and Drug Administration that should speed up the development of its treatment for a common...
FDA Approves Pneumococcal Vax Designed Specifically for Adults
MedPage Today· 2 days agoThe FDA approved a 21-valent pneumococcal conjugate vaccine (Capvaxive) for preventing invasive...
US FDA approves Merck’s pneumococcal vaccine for adults
WSAU Wausau· 2 days ago(Reuters) - Merck said on Monday the U.S. Food and Drug Administration has approved its...
FDA Ban On Shock Devices For Those With Developmental Disabilities Faces New Hurdle
Disability Scoop· 6 hours agoA bill making its way through the U.S. House of Representatives would limit the FDA’s ability to do...
Perspective: Ketamine, Matthew Perry and the coming wave of psychedelic medicine
Deseret News via Yahoo News· 5 hours agoFDA would not allow in research), with some clinics giving patients ketamine to take at home — a...
New drug hope for Alzheimers. Drug by Lilly may slow progression of disease and could get FDA...
KIVI Boise· 18 hours agoThe new drug from Ely Lilly - Donanemab - recently got approval from an FDA advisory panel. The FDA...
New FDA-Approved Treatment Offers Hope for Tinnitus Relief
KLAX-TV· 2 days agoA new FDA-approved treatment may help train the brain to ignore the ear ringing of tinnitus by...
Alzheimer's in Focus as FDA Panel Endorses Lilly's Donanemab (Revised)
Zacks via Yahoo Finance· 6 days agoIf Eli Lilly's (LLY) donanemab is approved by the FDA, it will become the second drug approved by...
Arizona health officials announce recall of candy, chocolate, gummies after illnesses reported
KSAZ via Yahoo News· 11 hours agoSafely dispose of any Diamond Shruumz-brand product you may have or return it to the retailer it was...