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
      OR
    • 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

  1. Xromi Prescribing Information. Nova Laboratories Ltd. Leicester, United Kingdom. December 2024.

  • 2025-04-03: New program for Xromi
  • 2025-04-03: New program for Xromi
  • 2025-04-03: New Program for Xromi

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