furosemide subcutaneous cartridge kit — Blue Cross Blue Shield of Illinois
Other FDA labeled indication for requested agent and route of administration
Initial criteria
- ONE of the following:
 - A. The patient has a diagnosis of edema with chronic heart failure or chronic kidney disease (including nephrotic syndrome) AND BOTH of the following:
 - 1. The patient was treated with an oral loop diuretic total daily dose of 40–160 mg furosemide equivalent AND
 - 2. The patient will NOT be using the requested agent in combination with another loop diuretic and will transition back to oral diuretic therapy after completion of the requested agent OR
 - B. The patient has another FDA labeled indication for the requested agent and route of administration AND
 - If the patient has an FDA labeled indication, then ONE of the following:
 - A. The patient’s age is within FDA labeling for the requested indication for the requested agent OR
 - B. There is support for using the requested agent for the patient’s age for the requested indication AND
 - The prescriber is a specialist in the area of the patient’s diagnosis (e.g., cardiologist, nephrologist), or the prescriber has consulted with a specialist in the area of the patient’s diagnosis AND
 - The patient does NOT have any FDA labeled contraindications to the requested agent
 
Reauthorization criteria
- Same as initial criteria
 
Approval duration
12 months