Product image of Icatibant Ethypharm (Icatibant) supplied by GNH India

Icatibant Ethypharm

Active Ingredient:
Icatibant
Origin:
EU

Icatibant Ethypharm (Icatibant)

Icatibant, the active ingredient in Icatibant Ethypharm, is a bradykinin B2 receptor antagonist presented as an injection solution for subcutaneous use. It is indicated for the treatment of acute attacks of hereditary angioedema in patients with C1‑inhibitor deficiency, helping to rapidly reduce swelling and restore normal airway function.
GNH India supplies Icatibant Ethypharm as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Ethypharm

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Indications & Clinical Uses

Icatibant acts on the bradykinin pathway to control swelling in hereditary angioedema.

  • Hereditary angioedema (C1‑inhibitor deficiency): provides rapid relief of acute swelling episodes and reduces the risk of airway obstruction.
  • Hereditary angioedema (acquired): may be used under specialist supervision to manage acute attacks.
  • Hereditary angioedema (type I/II): helps control symptoms when on‑demand therapy is required.

How It Works

  • Icatibant is a competitive antagonist of the bradykinin B2 receptor. By binding to this receptor, it blocks the actions of bradykinin, a peptide that causes vasodilation and increased vascular permeability. The inhibition prevents the cascade that leads to fluid extravasation and tissue swelling, thereby mitigating the acute manifestations of hereditary angioedema.

Side Effects

Icatibant may cause a range of adverse reactions following subcutaneous injection.

Common Side Effects

  • Injection site pain: mild to moderate discomfort at the injection site.
  • Redness or erythema: localized skin irritation.
  • Swelling at injection site: transient edema.
  • Nausea: occasional gastrointestinal upset.
  • Headache: mild to moderate intensity.
  • Dizziness: transient sensation of light‑headedness.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Severe hypotension: sudden drop in blood pressure.
  • Angioedema unrelated to HAE: unexpected swelling in other body parts.
  • Urticaria: widespread hives.
  • Severe allergic reaction: includes bronchospasm or throat tightening.
  • Thrombocytopenia: low platelet count observed in rare cases.

Precautions & Warnings

Before initiating therapy, clinicians should assess patient history and monitor for potential risks.

  • Assess C1‑inhibitor status: confirm deficiency before use.
  • Monitor for hypersensitivity: observe for signs of allergic reaction after each dose.
  • Avoid in known hypersensitivity: do not administer to patients with documented icatibant allergy.
  • Use with caution in pregnancy or breastfeeding: safety data are limited, weigh benefits against potential risks.
  • Evaluate renal and hepatic function: adjust monitoring if organ impairment is present.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Icatibant may interact with other agents that influence the bradykinin system or cause additive effects.

Major Interactions (Avoid)

  • ACE inhibitors: increased bradykinin levels may reduce icatibant efficacy and raise risk of angioedema.
  • Angiotensin‑converting enzyme‑derived peptides: concurrent use may potentiate swelling.

Moderate Interactions (Monitor Closely)

  • Estrogen‑containing contraceptives: may increase frequency of HAE attacks.
  • DPP‑4 inhibitors: theoretical increase in bradykinin activity.
  • Other B2 receptor antagonists: additive pharmacodynamic effects.
  • Immunosuppressants: monitor for altered infection risk.

Frequently Asked Questions

Icatibant Ethypharm is used to treat acute attacks of hereditary angioedema (HAE) in patients who have a deficiency of C1‑inhibitor. By rapidly blocking the effects of bradykinin, it helps reduce swelling of the skin, gastrointestinal tract, and airway, providing prompt symptom relief.

Icatibant works as a competitive antagonist of the bradykinin B2 receptor. By binding to this receptor, it prevents bradykinin from triggering vasodilation and increased vascular permeability, which are the primary mechanisms that cause the swelling seen in HAE attacks.

The dose of icatibant is determined by the prescribing clinician based on the patient’s condition and regulatory guidelines. Typically, a single subcutaneous injection is administered at the onset of an HAE attack, and additional doses may be given if needed under medical supervision.

Safety data for icatibant in pregnancy and lactation are limited, and the product is classified as having an unknown pregnancy category. Healthcare providers should weigh the potential benefits against any possible risks before prescribing it to pregnant or nursing women.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies, and procurement teams worldwide, and will request trade or institutional credentials before providing pricing, availability, shipping details (including cold‑chain if needed), and import documentation.

Icatibant is a bradykinin B2 receptor antagonist, whereas other approved therapies include C1‑inhibitor concentrates and kallikrein inhibitors. Icatibant offers a subcutaneous, on‑demand option that works directly at the receptor level, providing rapid symptom control without the need for intravenous infusion.

Icatibant should be stored at 2‑8 °C (refrigerated). Keep the vial in its original packaging, protect it from light, and avoid freezing or shaking the solution. If temporary storage at room temperature is unavoidable, limit exposure to no more than 30 °C for a short period.

Icatibant is administered as a subcutaneous injection, usually into the abdomen or thigh. The injection is performed by a trained healthcare professional or, in some cases, by the patient after proper instruction. The site should be rotated for each dose to minimize local irritation.

The most serious risks include severe allergic reactions such as anaphylaxis, sudden hypotension, and unexpected angioedema unrelated to HAE. Patients should be monitored closely after the first dose, and any signs of severe hypersensitivity require immediate medical intervention.

Icatibant should not be used in individuals with known hypersensitivity to the drug or any of its excipients. Caution is also advised for patients receiving ACE inhibitors or other agents that increase bradykinin levels, as the interaction may diminish therapeutic effectiveness.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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