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Pulmonary arterial hypertension

Pulmonary arterial hypertension is continuous high blood pressure in the pulmonary artery. The pulmonary artery carries blood from the right side of the heart to small arteries in the lungs.

In Pulmonary arterial hypertension, the arterial walls tighten, thicken, and scar. This leads to narrowing of the artery. In addition, tiny blood clots may cause blockage of blood flow.

All of these changes cause the right side of the heart to work harder to pump blood to the lungs. Over time, the heart weakens and cannot pump blood adequately. This may lead to right heart failure.

Although there is no cure for Pulmonary arterial hypertension, many treatment options are available. Treatment is based on the specific problem causing your condition. Medications that relax and open up the arteries to allow better circulation:

  • TracleerŽ (bosentan)
  • FlolanŽ (epoprostenol)
  • RemodulinŽ (treprostinil)
  • RevatioŽ (sildenafil)

Additional treatments may include anticoagulants (blood thinners), calcium channel blockers, and digitalis.

Diuretics (fluid pills) and oxygen are often used to relieve symptoms. Surgery is indicated only when required for removal of blood clots or, in severe cases, for lung or heart-lung transplant.

Your therapy

Walgreens will help you get the most from your therapy. Our specially trained pharmacists join your healthcare team, working together with your doctor and other providers to support your treatment plan.

To learn more about Walgreens' support services, call us toll free at 888-782-8443, or complete our online form.

Additional information is available to you through the following organizations:

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Information provided here does not constitute professional medical advice. Although it is intended to be accurate, neither Walgreen Co., its subsidiaries or affiliates, nor any other party assumes liability for loss or damage due to reliance on this material. If you have a medical question, consult your medical professional.

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