Name
209 Post-Launch Adverse Events Reported to FAERS for Long-Acting Injectable Buprenorphine
Description
This study analyzed FDA Adverse Event Reporting System data for Sublocade and Brixadi for the 12 months following their U.S. commercial launches. Adverse events were infrequent for both medications, supporting a favorable safety profile for long-acting injectable buprenorphine in the real-world treatment of moderate to severe opioid use disorder.
Speakers