Demser (metyrosine)
Indications for Prior Authorization
Demser (metyrosine)
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For diagnosis of Pheochromocytoma
Indicated for the treatment of patients with pheochromocytoma for preoperative preparation of patients for surgery, management of patients when surgery is contraindicated, and chronic treatment of patients with malignant pheochromocytoma. Metyrosine capsules are not recommended for the control of essential hypertension.
Criteria
Brand Demser, generic metyrosine
Prior Authorization
Length of Approval: 1 Time(s)
For diagnosis of Preoperative preparation
- Diagnosis of pheochromocytoma confirmed by one of the following biochemical testing:
- plasma free metanephrines
- urinary fractioned metanephrines
- Medication is being used for preoperative preparation AND
- Trial and failure, contraindication, or intolerance to both of the following:
- alpha-adrenergic blocker (e.g., phenoxybenzamine, doxazosin, terazosin)
- beta-adrenergic blocker (e.g., propranolol, metoprolol)
- Prescribed by or in consultation with one of the following:
- Endocrinologist
- Endocrine surgeon
Brand Demser, generic metyrosine
Prior Authorization (Initial Authorization)
Length of Approval: 6 Month(s)
For diagnosis of Treatment of pheochromocytoma
- Diagnosis of pheochromocytoma confirmed by one of the following biochemical testing:
- plasma free metanephrines
- urinary fractioned metanephrines
- Patient with hormonally active (catecholamine excess) pheochromocytoma AND
- One of the following:
- Patient is not a candidate for surgery OR
- Chronic treatment due to malignant pheochromocytoma
- Patient has not reached normotension after treatment with a selective alpha-1-adrenergic blocker (e.g., doxazosin, terazosin) and beta-adrenergic blocker (e.g., propranolol, metoprolol) AND
- Medication will not be used to control essential hypertension AND
- Prescribed by or in consultation with one of the following:
- Endocrinologist
- Provider who specializes in the management of pheochromocytoma
Brand Demser, generic metyrosine
Prior Authorization (Reauthorization)
Length of Approval: 12 Month(s)
For diagnosis of Treatment of pheochromocytoma
- Patient demonstrates positive clinical response to therapy (e.g., decreased frequency and severity of hypertensive attacks)
P & T Revisions
2024-03-14, 2023-09-13, 2023-03-01, 2022-10-26, 2022-03-01
References
- Metyrosine Prescribing Information. Amneal Pharmaceuticals LLC. Bridgewater, NJ. November 2020.
- Naruse M, Satoh F, Tanabe A, et al. Efficacy and safety of metyrosine in pheochromocytoma/paraganglioma: a multi-center trial in Japan. Endocrine Journal. 2018;65(3):359-371.
- Lenders JWM, Duh Q-Y, Eisenhofer G, et al. Pheochromocytoma and Paraganglioma: An Endocrine Society Clinical Practice Guideline. The Journal of Clinical Endocrinology & Metabolism. 2014;99(6):1915-1942.
Revision History
- 2024-03-14: 2024 Annual Review - no changes
- 2023-09-13: Program update to standard reauthorization language. No changes to clinical intent.
- 2023-03-01: 2023 Annual Review - no changes
- 2022-10-26: Attached EHB Formulary
- 2022-03-01: New Program