Specialty Pharmacy

In the United States, REMODULIN® (treprostinil) Injection is distributed by the following companies*:


Accredo Therapeutics
(866) 344-4874
http://www.accredotx.com


Curascript
(866) 474-8326
http://www.curascript.com


CVSCaremark
(877) 242-2738
http://www.caremark.com

*Disclaimer: Accredo Therapeutics, CuraScript Inc., and Caremark Inc. are separate independent specialty pharmaceutical services providers that provide medications and related services to patients in the home setting and have been contracted by United Therapeutics Corporation to distribute REMODULIN.

Specialty Pharmacy Service Offerings

  • All third-party reimbursement management
    • De novo patients
    • Patients transitioning from other PAH therapies
  • Patient assessment and evaluation
  • Pre-teaching
    • In home, hospital, or clinic
  • Coordination of services
  • Discharge planning support
  • Hotline access
    • Functions
    • Limitations
    • Service values

Continuous Specialty Pharmacy Support

  • PAH pump selection
  • Dosing sheets
  • Infusion site pain management support
  • Regular communication updates
    • Weekly or monthly, based on patient status
  • Drug monitoring
    • Efficacy
    • Adverse events
    • Drug interactions
  • Patient conviction and compliance with REMODULIN therapy

REMODULIN® (treprostinil) Injection

Indication

REMODULIN is indicated for the treatment of pulmonary arterial hypertension (PAH) in patients with NYHA Class II-IV symptoms to diminish symptoms associated with exercise. It may be administered as a continuous subcutaneous infusion or continuous intravenous infusion; however, because of the risks associated with chronic indwelling central venous catheters, including serious blood stream infections, continuous intravenous infusion should be reserved for patients who are intolerant of the subcutaneous route, or in whom these risks are considered warranted.

In patients with PAH requiring transition from Flolan® (epoprostenol sodium), REMODULIN is indicated to diminish the rate of clinical deterioration. The risks and benefits of each drug should be carefully considered prior to transition.

Important Safety Information:

Chronic intravenous infusions of REMODULIN are delivered using an indwelling central venous catheter. This route is associated with the risk of blood stream infections (BSI) and sepsis, which may be fatal. Therefore, continuous subcutaneous infusion is the preferred mode of administration. REMODULIN should be used only by clinicians experienced in the diagnosis and treatment of PAH. REMODULIN is a potent pulmonary and systemic vasodilator. It lowers blood pressure, which may be further lowered by other drugs that also reduce blood pressure. REMODULIN inhibits platelet aggregation and therefore, may increase the risk of bleeding, particularly in patients on anticoagulants. REMODULIN dosage adjustment may be necessary if inhibitors or inducers of CYP2C8 are added or withdrawn. Initiation of REMODULIN must be performed in a setting with adequate personnel and equipment for physiological monitoring and emergency care. Therapy with REMODULIN may be used for prolonged periods, and the patient’s ability to administer REMODULIN and care for an infusion system should be carefully considered. REMODULIN dosage should be increased for lack of improvement in, or worsening of, symptoms and it should be decreased for excessive pharmacologic effects or for unacceptable infusion site symptoms. Abrupt withdrawal or sudden large reductions in dosage of REMODULIN may result in worsening of PAH symptoms and should be avoided. Caution should be used in patients with hepatic or renal insufficiency.

The most common side effects of REMODULIN included those related to the method of infusion. For subcutaneous infusion, infusion site pain and infusion site reaction (redness and swelling) occurred in the majority of patients. These symptoms were often severe and could lead to treatment with narcotics or discontinuation of REMODULIN. For intravenous infusion, line infections, sepsis, arm swelling, tingling sensations, bruising, and pain were most common. General side effects (>5% more than placebo) were diarrhea, jaw pain, vasodilatation, and edema.

For more information about REMODULIN, please see the Full Prescribing Information.