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Photrexa – Enhanced & Essential

Commercial Policy
Version Date: July 2022

Utilization Management Policy Name: Photrexa – Enhanced & Essential

 

Restricted Product(s):

  • Photrexa® viscous (riboflavin 5’-phosphate)
  • Photrexa® (riboflavin 5’-phosphate)

 

FDA Approved Use:

  • Indicated for use with the KXL system in corneal collagen cross-linking for the treatment of progressive keratoconus and corneal ectasia following refractive surgery. 

 

Criteria for Approval of Restricted Product(s):

 

Initial Coverage

    1. The patient is 14 years of age or older; AND

    2. The patient has been diagnosed with ONE of the following (medical documentation required);

        1. Progressive keratoconus; OR

        2. Corneal ectasia following refractive surgery; AND

    3. The patient will use Photrexa in combination with corneal cross-linking procedure; AND

    4. The prescribed dose and quantity are appropriate based on intended use and FDA labeling; AND

    5. For formularies that exclude (non-formulary) the requested medication, Non-formulary Exception Criteria applies.

 

Duration of Approval:

30 days

 

References:

All information referenced is from FDA package insert unless otherwise noted below.

 

Policy Implementation/Update Information:

July 2022: Original utilization management policy issued