FDA Approves Zepbound: First Drug for Sleep Apnea

Tejal Somvanshi

FDA has approved Zepbound, marking the first medication authorized for treating moderate to severe obstructive sleep apnea in adults with obesity.

Photo Source: Blacktupelo (CC BY-SA 4.0)

Doctors say that FDA’s approval of Zepbound marks the first drug treatment option for certain patients with obstructive sleep apnea.

Photo Source: Kampus Production (Pexels)

The trials demonstrated that after 52 weeks of treatment, patients receiving Zepbound experienced measurable improvements in their apnea-hypopnea index.

Photo Source: @EliLillyandCo (X Formerly Twitter)

Patients not using CPAP machines showed approximately 25 fewer AHI breathing events per hour with Zepbound, compared to only five fewer events with placebo.

Photo Source: Russ (CC BY-NC-ND 2.0)

Weight loss results showed participants lost about 18% of their body weight, on average, in the first trial and about 20% in the second.

Photo Source: Click2pharmacy (CC BY 2.0)

Experts say that the availability of Zepbound as an option is relevant given that OSA affects approximately 30 million Americans, with obesity being a major contributing factor.

Photo Source: Photo By Kaboompics.com (Pexels)

The FDA reports several side effects, including gastrointestinal issues, injection site reactions, fatigue, hair loss, gastroesophageal reflux disease, etc.

Photo Source: Wendy Burchfield (CC BY 2.0)

Medicare’s current policy excludes coverage for weight-loss medications and will only be available to those above 65 to treat sleep apnea.

Photo Source: Nicola Barts (Pexels)

Photo Source: Nicola Barts (Pexels)

7,107 Duloxetine Bottles Recalled Over Cancer-Causing Contaminants