Tetrabenazine Prior Authorization (with Quantity Limit) Criteria - Medicare Part D
Medicare Utilization Management Policy
Version Date: January 1, 2025
Prior Authorization and Quantity Limit Criteria for Approval
Tetrabenazine will be approved when ALL of the following are met:
-
ONE of the following:
- The patient has a diagnosis of chorea associated with Huntington’s disease
OR - The patient has an indication that is supported in CMS approved compendia for the requested medication
AND
- The patient has a diagnosis of chorea associated with Huntington’s disease
-
ONE of the following:
- The patient does NOT have a current diagnosis of depression
OR - The patient has a current diagnosis of depression and is being treated for depression
AND
- The patient does NOT have a current diagnosis of depression
-
ONE of the following:
- The patient does NOT have a diagnosis of suicidal ideation and/or behavior
OR - The patient has a diagnosis of suicidal ideation and/or behavior and must NOT be actively suicidal
AND
- The patient does NOT have a diagnosis of suicidal ideation and/or behavior
-
The patient will NOT be using the requested medication in combination with a monoamine oxidase inhibitor (MAOI)
AND -
The patient will NOT be using the requested medication in combination with reserpine
AND -
The patient does NOT have any FDA labeled contraindications to the requested medication
AND -
ONE of the following:
-
The requested quantity (dose) does NOT exceed the program quantity limit
OR -
ALL of the following
- The requested quantity (dose) is greater than the program quantity limit
AND - The requested quantity (dose) cannot be achieved with a lower quantity of a higher strength that does not exceed the program quantity limit
AND - The prescriber has submitted information in support of therapy with a higher dose for the requested indication
- The requested quantity (dose) is greater than the program quantity limit
-
Length of Approval: 12 months