Intrarosa (prasterone)
Indications for Prior Authorization
Intrarosa (prasterone)
-
For diagnosis of Moderate to Severe Dyspareunia
Indicated for the treatment of moderate to severe dyspareunia, a symptom of vulvar and vaginal atrophy, due to menopause.
Criteria
Intrarosa
Step Therapy
Length of Approval: 12 Month(s)
- Requested drug is being used for a Food and Drug Administration (FDA)-approved indication AND
- Trial and failure (of a minimum 28-day supply), contraindication, or intolerance to one of the following:
- Premarin vaginal cream
- Osphena
P & T Revisions
2024-06-20, 2023-05-10, 2022-06-02, 2021-07-07, 2020-09-02
References
- Intrarosa prescribing information. AMAG Pharmaceuticals, Inc. Waltham, MA. February 2018.
Revision History
- 2024-06-20: 2024 UM Annual Review. No criteria changes
- 2023-05-10: 2023 UM Annual Review. Updated trial duration to 28 days supply
- 2022-06-02: Updated criteria.
- 2021-07-07: New program
- 2020-09-02: New Program