Patients should always discuss adverse events with their healthcare providers.

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

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


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



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