Alosetron Prior Authorization with Quantity Limit Criteria - Medicare Part D
Prior Authorization Criteria for Approval
Alosetron will be approved when ALL of the following are met:
- The patient has a diagnosis of irritable bowel syndrome with severe diarrhea (IBS-D) AND
- The patient’s sex is female AND
- The patient exhibits at least ONE of the following
- Frequent and severe abdominal pain/discomfort OR
- Frequent bowel urgency or fecal incontinence OR
- Disability or restriction of daily activities due to IBS AND
- The prescriber has ruled out anatomic or biochemical abnormalities of the gastrointestinal tract 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 provided information in support of therapy with a higher dose for the requested indication
Length of Approval: 12 months
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