Product image of Iloprost Rafarm (Iloprost) supplied by GNH India

Iloprost Rafarm

Active Ingredient:
Iloprost
Origin:
EU

Iloprost Rafarm (Iloprost)

Iloprost, the active ingredient in Iloprost Rafarm, is a prostacyclin analogue presented as an inhalation solution for inhalation use. It treats pulmonary arterial hypertension and digital ulcers associated with systemic sclerosis in adult patients.

GNH India supplies Iloprost Rafarm as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Rafarm Sa.

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Indications & Clinical Uses

Iloprost Rafarm is a prostacyclin analogue used in the management of vascular disorders affecting the pulmonary circulation and skin.

  • Pulmonary arterial hypertension: improves exercise capacity, delays disease progression, and reduces pulmonary vascular resistance.
  • Digital ulcers associated with systemic sclerosis: promotes ulcer healing and reduces the formation of new ulcers.
  • Adjunct therapy in PAH: provides inhaled vasodilation for patients unsuitable for oral or intravenous prostacyclin therapy.

How It Works

  • Iloprost is a synthetic prostacyclin analogue that selectively activates the IP (prostacyclin) receptor on vascular smooth‑muscle cells. Receptor activation increases cyclic AMP levels, leading to potent vasodilation of pulmonary arteries and inhibition of platelet aggregation, thereby improving pulmonary hemodynamics and tissue perfusion.

Side Effects

Iloprost may cause a range of adverse reactions, most of which are mild and reversible.

Common Side Effects

  • Cough: irritation of the airway during inhalation.
  • Throat irritation: discomfort or soreness in the throat.
  • Headache: mild to moderate intensity.
  • Nausea: occasional feeling of queasiness.
  • Flushing: transient warmth and redness of the skin.
  • Dizziness: light‑headed sensation, especially on standing.

Serious or Rare Side Effects

  • Hypotension: significant drop in blood pressure requiring medical attention.
  • Pulmonary edema: fluid accumulation in the lungs.
  • Severe bronchospasm: acute narrowing of the airways.
  • Bleeding events: increased risk of hemorrhage.
  • Chest pain: angina‑like discomfort.
  • Cardiac arrhythmia: irregular heart rhythm.

Precautions & Warnings

Before initiating Iloprost therapy, clinicians should consider several safety measures.

  • Blood pressure monitoring: check for hypotension before and during treatment.
  • Bleeding risk assessment: evaluate concurrent anticoagulant use.
  • Respiratory status: avoid in patients with active severe asthma or COPD exacerbations.
  • Recent hemoptysis: contraindicated in patients with recent coughing up of blood.
  • Pregnancy and lactation: use only if potential benefit justifies potential risk.
  • Store at room temperature: keep in original container, protect from moisture and light.

Avoid Interactions

Iloprost can interact with other medications that affect vascular tone or coagulation.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): may increase bleeding risk.
  • Endothelin receptor antagonists: additive hypotensive effect.
  • Phosphodiesterase‑5 inhibitors: excessive vasodilation and hypotension.

Moderate Interactions (Monitor Closely)

  • Aspirin and other NSAIDs: may enhance bleeding tendency.
  • Beta‑blockers: may blunt the desired vasodilatory response.
  • Calcium channel blockers: potential additive blood pressure lowering effect.

Frequently Asked Questions

Iloprost Rafarm is indicated for the treatment of pulmonary arterial hypertension and for the management of digital ulcers associated with systemic sclerosis. It works by dilating the pulmonary vessels and improving blood flow to the skin, helping to reduce symptoms and disease progression.

Iloprost is a synthetic prostacyclin analogue that activates IP receptors on vascular smooth‑muscle cells. This activation raises cyclic AMP levels, causing vasodilation of pulmonary arteries and inhibiting platelet aggregation, which together improve pulmonary hemodynamics and tissue perfusion.

The dose of Iloprost Rafarm is individualized by the prescribing clinician based on the patient’s condition, severity, and response to therapy. The prescriber determines the appropriate inhalation volume, frequency, and duration according to clinical guidelines and patient tolerance.

Safety data for Iloprost Rafarm in pregnancy and lactation are limited. It should only be used if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision should be made by a qualified healthcare professional.

To request Iloprost Rafarm, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if needed), and import documentation.

Iloprost is an inhaled prostacyclin analogue, offering rapid pulmonary vasodilation with a short half‑life, unlike oral endothelin antagonists or intravenous prostacyclin infusions. It is often chosen for patients who prefer inhalation over continuous infusion and who need targeted pulmonary artery dilation.

Iloprost Rafarm should be stored at room temperature, below 25 °C, in its original packaging. Protect the solution from moisture, direct sunlight, and extreme temperatures to maintain its stability and efficacy.

Iloprost Rafarm is supplied as an inhalation solution. The patient uses a certified nebulizer device to inhale the medication, typically several times per day as directed by the prescriber. Proper inhalation technique and device cleaning are essential for optimal delivery.

Serious risks include marked hypotension, pulmonary edema, severe bronchospasm, bleeding complications, chest pain, and cardiac arrhythmias. Patients should be monitored closely for these events, especially during dose titration or when combined with other vasodilators.

Iloprost Rafarm is contraindicated in patients with known hypersensitivity to iloprost or any component of the formulation, recent hemoptysis, severe uncontrolled asthma or COPD, and those with unstable cardiovascular conditions where rapid vasodilation could be hazardous.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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