Exenatide (Byetta®), Exenatide extended release (Bydureon®, Bydureon BCise®)
SELF ADMINISTRATION
Indications for Prior Authorization:
- Adjunctive therapy to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus
The following indications do not meet the criteria for use established by the Western Health Advantage Pharmacy and Therapeutics Committee:
- Treatment of Type 1 diabetes
- Treatment of ketoacidosis
- Appetite suppression or treatment of obesity
All of the following must be met as a condition(s) for coverage:
- Diagnosis of Type 2 diabetes confirmed by chart note documentation, AND
- Trial and failure of metformin
- DPP4 (dipeptidyl peptidase-4) inhibitors are not approvable with concurrent administration of GLP-1 (glucagon-like peptide-1) agonists
- Exenatide (Byetta®), Exenatide Extended-Release (Bydureon®, Bydureon BCise®), Liraglutide (Victoza®), Semaglutide (Ozempic®, Rybelsus®), Dulaglutide (Trulicity®) are the preferred agents
Dosing:
Exenatide (Byetta®)
- Initiate at 5 mcg SubQ twice a day within the 60 minute period before the morning and evening meals. If an inadequate response, then dose may be increased to 10 mcg twice a day after one month
Exenatide extended release (Bydureon®, Bydureon BCise®)
- Inject 2 mg SubQ every week
Approval:
- 1 year
Last review date: July 30, 2020