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Inhaled Ventavis® (iloprost) Inhalation Solution Breathe In the Power of Prostacyclin In Pulmonary Arterial Hypertension (PAH) NYHA Class III or IV
About PAH
PAH Pathways - Actelion Services & Support
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About PAH

Pulmonary arterial hypertension (PAH) is a devastating disease. Before the introduction of modern therapies, on average, patients survived only 2.5 years.1 Fortunately, treatment options have expanded over the last decade and now include 6 FDA-approved medications. With these expanded treatment options, the prognosis is improving2 and patients are living longer than historical predictions indicated. PAH therapies, including Ventavis® (iloprost), have had a positive impact on clinical status, exercise capacity, functional class, and hemodynamics.

Pulmonary Arterial Hypertension Defined

Mean pulmonary artery pressure (mPAP) ≥ 25 mm Hg with a pulmonary capillary wedge pressure ≤ 15 mm Hg measured by cardiac catheterization1

Read more about Ventavis:

1. Badesch DB, Abman SH, Simonneau G, Rubin LJ, and McLaughlin, V V. Medical Therapy for Pulmonary Arterial Hypertension. Chest 2007;131:1917-1928.
2. Chin KM, Rubin LF. Pulmonary Arterial Hypertension. J Am Coll Cardiol 2008;51:1527-38)



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