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  • Medications for Pulmonary Arterial Hypertension

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    21 results
    • adcirca

      (Tadalafil)
      United Therapeutics Corporation
      Usage: ADCIRCA® is indicated for treating pulmonary arterial hypertension (PAH) (WHO Group 1) to enhance exercise capacity. It has been primarily studied in patients with NYHA Functional Class II-III symptoms, including cases of idiopathic or heritable PAH and PAH linked to connective tissue diseases.
    • alyq

      (Tadalafil)
      Teva Pharmaceuticals Inc
      Usage: ALYQ® (tadalafil tablets) is indicated for the treatment of pulmonary arterial hypertension (PAH) to improve exercise ability in patients, particularly those with NYHA Functional Class II-III symptoms, including idiopathic, heritable PAH, and PAH tied to connective tissue diseases.
    • ambrisentan

      (ambrisentan)
      Sun Pharmaceutical Industries, Inc.
      Usage: Ambrisentan is indicated for treating pulmonary arterial hypertension (PAH) to improve exercise capacity and delay clinical worsening, primarily in patients with WHO Functional Class II–III symptoms and idiopathic, heritable, or connective tissue disease-associated PAH.
    • bosentan

      (bosentan)
      Actavis Pharma, Inc.
      Usage: Bosentan tablets are indicated for treating pulmonary arterial hypertension (PAH) in adults and pediatric patients aged 3 and older. In adults, it improves exercise ability and decreases clinical worsening, while in children, it aims to improve pulmonary vascular resistance, enhancing exercise performance.
    • bosentan

      (Bosentan)
      Amneal Pharmaceuticals LLC
      Usage: Bosentan tablets are indicated for treating pulmonary arterial hypertension (PAH) in adults. They improve exercise ability and reduce clinical worsening in patients with WHO Functional Class II-IV symptoms due to idiopathic or heritable PAH, connective tissue diseases, or congenital heart disease with left-to-right shunts.
    • bosentan

      (Bosentan)
      Zydus Pharmaceuticals USA Inc.
      Usage: Bosentan tablets are indicated for treating pulmonary arterial hypertension (PAH) in adults. They improve exercise ability and reduce clinical worsening, particularly in patients with WHO Functional Class II-IV symptoms related to idiopathic or heritable PAH, connective tissue diseases, and congenital heart disease with left-to-right shunts.
    • epoprostenol

      (EPOPROSTENOL)
      Mylan Institutional LLC
      Usage: Epoprostenol for injection is indicated for treating pulmonary arterial hypertension (PAH) to improve exercise capacity, primarily in patients with NYHA Functional Class III-IV symptoms, including those with idiopathic, heritable PAH, or PAH associated with connective tissue diseases.
    • letairis

      (AMBRISENTAN)
      Gilead Sciences, Inc
      Usage: Letairis is indicated for treating pulmonary arterial hypertension (PAH) to improve exercise capacity, delay clinical worsening, and reduce disease progression and hospitalization risks when combined with tadalafil. It is primarily studied in patients with WHO Functional Class II–III symptoms related to idiopathic, heritable PAH, or connective tissue diseases.
    • opsumit

      (macitentan)
      Actelion Pharmaceuticals US, Inc.
      Usage: OPSUMIT is indicated for treating pulmonary arterial hypertension (PAH, WHO Group I) to reduce disease progression and hospitalization risks. Its effectiveness was demonstrated in a long-term study involving patients with various forms of PAH, primarily those with WHO Functional Class II–III symptoms.
    • orenitram

      (treprostinil)
      United Therapeutics Corporation
      Usage: Orenitram is indicated for treating pulmonary arterial hypertension (PAH) to delay disease progression and improve exercise capacity, primarily in patients with WHO functional class II-III symptoms, including idiopathic, heritable, or connective tissue disease-associated PAH.