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furosemide subcutaneous cartridge kitBlue Cross Blue Shield of Montana

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 has consulted with such a specialist AND
  • The patient does NOT have any FDA labeled contraindications to the requested agent

Approval duration

12 months