Xromi (hydroxyurea)
Indications for Prior Authorization
Xromi (hydroxyurea)
-
For diagnosis of Sickle Cell Anemia
Indicated to reduce the frequency of painful crises and reduce the need for blood transfusions in pediatric patients aged 6 months of age and older with sickle cell anemia with recurrent moderate to severe painful crises.
Criteria
Xromi
Prior Authorization (Initial Authorization)
Length of Approval: 12 Month(s)
- Diagnosis of sickle cell anemia AND
- Patient has moderate to severe painful crises AND
- Patient is 6 months of age or older AND
- One of the following:
- Patient is unable to swallow solid oral dosage forms (e.g., oral tablet, capsule) due to one of the following:
- Age
- Physical impairment (e.g., difficulties with motor or oral coordination)
- Dysphagia
- Patient is using a feeding tube or nasal gastric tube
- Dosage requirements cannot be met with a solid dosage form
Xromi
Prior Authorization (Reauthorization)
Length of Approval: 12 Month(s)
- Patient demonstrates positive clinical response to therapy
P & T Revisions
2025-04-03, 2025-04-03, 2025-04-03
References
- Xromi Prescribing Information. Nova Laboratories Ltd. Leicester, United Kingdom. December 2024.
Revision History
- 2025-04-03: New program for Xromi
- 2025-04-03: New program for Xromi
- 2025-04-03: New Program for Xromi