tolvaptan — Blue Cross Blue Shield of Kansas
clinically significant hypervolemic hyponatremia
Initial criteria
- Requested agent was initiated (or re-initiated) in the hospital AND
- Prior to initiating therapy, patient has/had clinically significant hypervolemic or euvolemic hyponatremia defined by ONE of the following: (A) serum sodium <125 mEq/L OR (B) serum sodium ≥125 mEq/L and symptomatic hyponatremia that has resisted correction with fluid restriction AND
- Patient does NOT have underlying liver disease, including cirrhosis AND
- Medications known to cause hyponatremia have been evaluated and discontinued when appropriate AND
- Patient will NOT be using the requested agent in combination with another tolvaptan product for the requested indication AND
- Patient does not have any FDA labeled contraindications to the requested agent AND
- Patient has not already received 30 days of therapy with the requested agent for the current hospitalization
Approval duration
365 days