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FDA Approves First Medication for Obstructive Sleep Apnea

By Drug Administration
From Livingston County News

FDA Approves First Medication for Obstructive Sleep Apnea

SILVER SPRING, Md., Dec. 20, 2024 /PRNewswire/ -- Today, the U.S. Food and Drug Administration approved Zepbound (tirzepatide) for the treatment of moderate to severe obstructive sleep apnea (OSA) in adults with obesity, to be used in combination with a reduced-calorie diet and increased physical activity.

"Today's approval marks the first drug treatment option for certain patients with obstructive sleep apnea," said Sally Seymour, M.D., director of the Division of Pulmonology, Allergy, and Critical Care in the FDA's Center for Drug Evaluation and Research. "This is a major step forward for patients with obstructive sleep apnea."

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