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Vfend (voriconazole)Blue Cross Blue Shield of Montana

other deep tissue Candida infection

Preferred products

  • fluconazole

Initial criteria

  • Patient has diagnosis of invasive aspergillosis OR
  • Patient receiving prophylaxis of invasive aspergillosis or Candida and is severely immunocompromised (hematopoietic stem cell transplant recipient, hematologic malignancy with prolonged neutropenia, or high-risk solid organ transplant recipient) OR
  • Patient has diagnosis of esophageal candidiasis, candidemia, or other deep tissue Candida infection AND one of the following: (A) meets stage four advanced metastatic cancer criteria with use consistent with best practices; (B) tried and inadequately responded to fluconazole; (C) intolerance or hypersensitivity to fluconazole; (D) FDA labeled contraindication to fluconazole OR
  • Patient has serious infection caused by Scedosporium or Fusarium species OR
  • Patient has another FDA labeled indication or compendia-supported indication for requested agent and route AND patient’s age is appropriate or supported for use AND patient has no FDA labeled contraindication
  • Compendia Allowed: AHFS or DrugDex 1, 2a, or 2b level of evidence

Reauthorization criteria

  • Patient previously approved for requested agent through prior authorization process AND
  • Patient has one of the following: (A) diagnosis of invasive aspergillosis, serious infection caused by Scedosporium or Fusarium species, esophageal candidiasis, candidemia, or deep tissue Candida infection AND continued clinical need documented

Approval duration

6 months