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For PAH (WHO Group 1) to diminish symptoms associated with exercise and to diminish the rate of clinical deterioration in patients transitioning from Flolan® (epoprostenol sodium).

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The Remodulin SPmix Program delivers up to 7 days of premixed IV Remodulin and all necessary supplies to your patients’ homes each week.

Remodulin is a prostacyclin vasodilator indicated for the treatment of pulmonary arterial hypertension (PAH; WHO Group 1) to diminish symptoms associated with exercise. Studies establishing effectiveness included patients with NYHA Functional Class II-IV symptoms and etiologies of idiopathic or heritable PAH (58%), PAH associated with congenital systemic-to-pulmonary shunts (23%), or PAH associated with connective tissue diseases (19%).

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In patients with PAH requiring transition from epoprostenol, Remodulin is indicated to diminish the rate of clinical deterioration. Consider the risks and benefits of each drug prior to transition.

To ensure patients receive your choice of Remodulin® (treprostinil), make sure to indicate “Dispense as Written, Brand Medically Necessary, and No Substitution” in the Prescriber Signature section of the Referral Form.

In patients with PAH requiring transition from epoprostenol, Remodulin is indicated to diminish the rate of clinical deterioration. Consider the risks and benefits of each drug prior to transition.

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All other brands are trademarks of their respective owners. The makers of these brands are not affiliated with and do not endorse United Therapeutics or its products.

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The CADD®-Solis VIP ambulatory infusion pump is reliable for the continuous IV delivery of Remodulin and other medicines.1

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References: 1. Smiths Medical. CADD-Solis VIP™ Comparison Sheet. 2022. 2. Smiths Medical. CADD-Solis VIP™ Ambulatory Infusion System Brochure English. 2022. 3. Remodulin [package insert]. Research Triangle Park, NC: United Therapeutics Corporation; 2023.

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Remodulin is a prostacyclin vasodilator indicated for the treatment of pulmonary arterial hypertension (PAH; WHO Group 1) to diminish symptoms associated with exercise. Studies establishing effectiveness included patients with NYHA Functional Class II-IV symptoms and etiologies of idiopathic or heritable PAH (58%), PAH associated with congenital systemic-to-pulmonary shunts (23%), or PAH associated with connective tissue diseases (19%).

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