The FDA approved the Amplatzer PFO Occluder device to reduce stroke risk in patients who have had a stroke from a blood clot passing through a patent foramen ovale.
The FDA has approved class-wide labeling changes for all prescription testosterone products with information regarding the risks of abuse and dependence.
The FDA approved a new method of administering treatment for patients with wet age-related macular degeneration and macular edema following retinal vein occlusion.
The US Food and Drug Administration is now requiring a Boxed Warning be added to the drug labels of certain direct-acting antiviral medicines used for the treatment of hepatitis C.
The FDA approved a biologic to treat adults with active Crohn disease who have failed or were intolerant to treatment with immunomodulators or corticosteroids.