Patients should always discuss adverse events with their healthcare providers.

Patients are encouraged to report adverse events related to LIKMEZ^TM by calling 1-833-727-8254 (U.S. only). Patients may also contact the U.S. Food and Drug Administration (FDA) directly. Visit www.fda.gov/medwatch or call 1-800-FDA-1088.

This site is intended only for U.S. residents.

Email: drugsafety@saptalis.com

Saptalis Pharmaceuticals, LLC.
45 Davids Dr.
Hauppauge, New York 11788
USA