SILVER SPRING, Md. /PRNewswire/ — Today, the U.S. Food and Drug Administration approved Veozah (fezolinetant), an oral medication for the treatment of moderate to severe vasomotor symptoms, or hot...
Today, the U.S. Food and Drug Administration approved Vyjuvek, a herpes-simplex virus type 1 (HSV-1) vector-based gene therapy, for the treatment of wounds in patients 6...
FDA clears Beta Bionics iLet ACE Pump & iLet Dosing Decision Software for people with type 1 diabetes.
FDA approves first RSV vaccine, Arexvy, for those 60+ reducing risk of severe LRTD by 94.1%.
The U.S. Food and Drug Administration (FDA) has amended the emergency use authorizations (EUAs) of the Moderna and Pfizer-BioNTech COVID-19 bivalent mRNA vaccines to simplify the...
The FDA has recently approved a cell therapy called Omisirge (omidubicel-onlv) for patients with blood cancers who are undergoing stem cell transplantation. This allogeneic cord blood-based...
The FDA has approved the Azure Fastep COVID-19 Antigen Pen Home Test, a quick and convenient option for serial testing for symptomatic and asymptomatic individuals.
The FDA warns about hand sanitizer safety and advises following the Drug Facts label and safety tips to avoid harm from toxic substances, accidental fires, eye...
Agency Continues to Take Steps to Reduce New Cases of Opioid Use Disorder
The U.S. Food and Drug Administration released a national strategy outlining actions the agency will take immediately to help ensure one of the nation’s most vulnerable...
