Pulmonary Arterial Hypertension
Pulmonary arterial hypertension (PAH) is a distinct subgroup of pulmonary hypertension that comprises idiopathic PAH, familial/heritable forms, and PAH associated with connective tissue disease, congenital heart disease, portal hypertension, human immunodeficiency virus (HIV) infection, and some other conditions. PAH is a life-threatening condition which gets worse over time.
City Drugs is here to give you the support your need when you need it. If you have any questions about the medications we provide for patients with chronic, complex conditions, feel free to contact us at 212-988-4500 or click here