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

Iloprost Teva

Active Ingredient:
Iloprost
Origin:
EU

Iloprost Teva (Iloprost)

Iloprost, the active ingredient in Iloprost Teva, is a prostacyclin analog presented as an injectable solution for intravenous and subcutaneous use. It is employed to manage pulmonary arterial hypertension, digital ulcers linked to systemic sclerosis, and peripheral arterial disease in adult patients.

GNH India supplies Iloprost Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory support for cross‑border distribution, ensuring product integrity throughout the supply chain.

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

  • Iloprost is indicated for several vascular conditions where prostacyclin pathways are compromised.
  • Pulmonary arterial hypertension: reduces pulmonary arterial pressure, improves functional class, and increases six‑minute walk distance in affected adults.
  • Digital ulcers associated with systemic sclerosis: accelerates ulcer closure, decreases pain, and lowers the incidence of new digital lesions.
  • Peripheral arterial disease: mitigates ischemic pain during walking, improves walking distance, and supports tissue perfusion in patients with limb ischemia.

How It Works

  • Iloprost is a synthetic analogue of prostacyclin (PGI2) that binds to prostacyclin (IP) receptors on vascular smooth‑muscle cells. Activation of the IP receptor stimulates adenylate cyclase, raising intracellular cyclic‑AMP levels, which leads to vasodilation, inhibition of platelet aggregation, and antiproliferative effects on the vascular wall, thereby improving blood flow in the pulmonary and peripheral circulations. These actions collectively reduce pulmonary vascular resistance and support microvascular repair.

Side Effects

Iloprost may be associated with a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Headache: mild to moderate intensity, often transient.
  • Flushing: warmth and reddening of the skin.
  • Nausea: occasional gastrointestinal discomfort.
  • Jaw pain: mild discomfort during infusion.
  • Diarrhea: loose stools during treatment.
  • Peripheral edema: swelling of the limbs.

Serious or Rare Side Effects

  • Hypotension: significant drop in blood pressure requiring medical intervention.
  • Bleeding: increased risk of hemorrhage due to platelet inhibition.
  • Pulmonary edema: fluid accumulation in the lungs, a rare but serious event.

Precautions & Warnings

When prescribing Iloprost, clinicians should observe several precautionary measures to ensure patient safety.

  • Dose titration: start with low dose and increase gradually under medical supervision.
  • Cardiovascular monitoring: regularly assess blood pressure and heart rate during therapy.
  • Bleeding risk: evaluate coagulation status and avoid concomitant anticoagulants unless necessary.
  • Renal impairment: adjust therapy in patients with severe kidney dysfunction.
  • Pregnancy and lactation: avoid use unless benefits outweigh potential risks.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Iloprost can interact with other medicines, influencing its efficacy or safety profile.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin, heparin): additive antiplatelet effect may increase bleeding risk.
  • Phosphodiesterase‑5 inhibitors (e.g., sildenafil): may cause profound hypotension.
  • Endothelin receptor antagonists (e.g., bosentan): potential for enhanced vasodilatory response.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may affect renal function and platelet activity.
  • Calcium channel blockers: possible additive blood pressure lowering effect.
  • Beta‑blockers: may mask tachycardia associated with hypotension.

Frequently Asked Questions

Iloprost Teva is prescribed for pulmonary arterial hypertension, digital ulcers associated with systemic sclerosis, and peripheral arterial disease. In each case, the drug helps improve blood flow by dilating vessels and reducing platelet aggregation, which can alleviate symptoms and slow disease progression.

Iloprost mimics the natural prostacyclin molecule, binding to IP receptors on vascular smooth‑muscle cells. This triggers an increase in cyclic‑AMP, causing the muscles to relax, which widens blood vessels, lowers pulmonary pressure, and inhibits platelet clumping, thereby enhancing circulation.

The specific dose and infusion schedule for Iloprost are set by the prescribing clinician based on the patient’s diagnosis, severity of disease, response to therapy, and any concurrent medical conditions. Dosage adjustments are made according to clinical monitoring and tolerance.

Safety data for Iloprost in pregnancy and lactation are limited. The drug should be used only if the potential benefits justify the possible risks to the fetus or infant, and the decision must be made by a qualified healthcare professional.

To place an order, submit an enquiry on the Iloprost Teva 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 where required) and necessary import documentation.

Iloprost is a synthetic prostacyclin analog that can be administered intravenously or subcutaneously, offering flexibility compared with some prostacyclin agents that require continuous infusion. Its short half‑life allows for titrated dosing, but it may require more frequent administration than longer‑acting formulations such as treprostinil or epoprostenol.

Iloprost Teva should be stored at 2‑8 °C (refrigerated). Keep the product in its original packaging, protect it from light, and avoid freezing or shaking the vial, as temperature excursions can affect stability and potency.

Iloprost is supplied as a sterile injectable solution and can be given either intravenously or subcutaneously. The route, infusion rate, and duration are determined by the treating physician, who monitors the patient for therapeutic response and any adverse effects during administration.

The most serious risks include severe hypotension, which can lead to dizziness or syncope, and bleeding complications due to its antiplatelet activity. Rarely, patients may develop pulmonary edema. Prompt medical evaluation is required if any of these events occur.

Iloprost is contraindicated in patients with known hypersensitivity to the drug or its excipients, those with uncontrolled severe hypotension, active bleeding disorders, or recent major surgery where platelet inhibition could be hazardous. Clinicians should also exercise caution in patients with significant renal impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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