Pulmoris Tablet 10's

Pulmoris Tablet 10's

Prescription drug
Manufacturer / Marketer : ETABX
Expiry : 31-10-2027
AboutPulmoris Tablet contains ambrisentan, an endothelin receptor antagonist used for the treatment of pulmonary arterial hypertension (PAH) in adults with WHO functional class II, III, or IV symptoms, including idiopathic PAH and PAH associated with connective tissue disease.Usage InstructionsTake once daily as prescribed by your specialist physician, with or without food. Swallow whole with water. Do not stop or change dose without consulting your doctor. Regular monitoring required.Benefits- Improves exercise capacity in PAH patients- Reduces pulmonary arterial pressure- Delays clinical worsening- Improves WHO functional class- Enhances quality of life- Specific treatment for pulmonary hypertensionHow it WorksAmbrisentan selectively blocks endothelin-1 receptors on blood vessel walls, preventing vasoconstriction and vascular remodeling in pulmonary arteries, thereby reducing pulmonary pressure and improving blood flow to lungs.Side EffectsCommon: Headache, flushing, nasal congestion, peripheral edema (swelling of legs/ankles), palpitations. Less common: Anemia, liver enzyme elevation. Serious: Birth defects (teratogenic), liver toxicity.Safety Advice- Strict prescription and specialist monitoring required- CONTRAINDICATED in pregnancy (can cause severe birth defects)- Women of childbearing potential must use reliable contraception- Monthly pregnancy tests required during treatment- Regular liver function monitoring needed- Not for use in severe liver impairment- Inform doctor of all medications (drug interactions possible)StorageStore below 30°C in original packaging. Protect from moisture and light. Keep out of reach of children. Do not use beyond expiry date.
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AboutPulmoris Tablet contains ambrisentan, an endothelin receptor antagonist used for the treatment of pulmonary arterial hypertension (PAH) in adults with WHO functional class II, III, or IV symptoms, including idiopathic PAH and PAH associated with connective tissue disease.Usage InstructionsTake once daily as prescribed by your specialist physician, with or without food. Swallow whole with water. Do not stop or change dose without consulting your doctor. Regular monitoring required.Benefits- Improves exercise capacity in PAH patients- Reduces pulmonary arterial pressure- Delays clinical worsening- Improves WHO functional class- Enhances quality of life- Specific treatment for pulmonary hypertensionHow it WorksAmbrisentan selectively blocks endothelin-1 receptors on blood vessel walls, preventing vasoconstriction and vascular remodeling in pulmonary arteries, thereby reducing pulmonary pressure and improving blood flow to lungs.Side EffectsCommon: Headache, flushing, nasal congestion, peripheral edema (swelling of legs/ankles), palpitations. Less common: Anemia, liver enzyme elevation. Serious: Birth defects (teratogenic), liver toxicity.Safety Advice- Strict prescription and specialist monitoring required- CONTRAINDICATED in pregnancy (can cause severe birth defects)- Women of childbearing potential must use reliable contraception- Monthly pregnancy tests required during treatment- Regular liver function monitoring needed- Not for use in severe liver impairment- Inform doctor of all medications (drug interactions possible)StorageStore below 30°C in original packaging. Protect from moisture and light. Keep out of reach of children. Do not use beyond expiry date.

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