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 a subcutaneous injection for subcutaneous use. It is indicated for the treatment of acute attacks of hereditary angioedema (HAE) in patients with type I or type II disease.
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 relieve swelling in hereditary angioedema.

  • Hereditary angioedema type I: rapid reduction of swelling during acute attacks.
  • Hereditary angioedema type II: rapid reduction of swelling during acute attacks.
  • Acute HAE attacks in adults: provides prompt symptom relief and shortens attack duration.

How It Works

  • Icatibant selectively blocks the bradykinin B2 receptor, preventing bradykinin from binding and activating the receptor. This inhibition stops bradykinin‑mediated vasodilation and increased vascular permeability, thereby reducing the edema and swelling characteristic of hereditary angioedema attacks.

Side Effects

Icatibant may cause a range of adverse reactions, most of which are related to the injection site or systemic hypersensitivity.

Common Side Effects

  • Injection site pain: mild to moderate discomfort at the injection site.
  • Redness: localized erythema around the injection area.
  • Swelling: transient edema at the site of administration.
  • Warmth: sensation of heat at the injection site.
  • Nausea: occasional mild gastrointestinal upset.
  • Headache: transient mild headache.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Angioedema: unexpected swelling of face, lips, or throat.
  • Hypotension: sudden drop in blood pressure.
  • Thrombocytopenia: reduced platelet count observed in rare cases.
  • Severe injection site reactions: necrosis or ulceration.

Precautions & Warnings

Before using Icatibant, consider the following safety measures.

  • Hypersensitivity: avoid if known allergy to icatibant or any formulation component.
  • Pregnancy: use only if potential benefit justifies potential risk, as safety data are limited.
  • Breastfeeding: discontinue nursing or discontinue the drug, based on clinical judgment.
  • Concomitant ACE inhibitors: monitor closely for enhanced bradykinin effects.
  • Renal impairment: no dose adjustment required, but monitor clinical response.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Icatibant may interact with other medicines that influence the bradykinin system.

Major Interactions (Avoid)

  • ACE inhibitors: increased bradykinin levels may heighten risk of angioedema.
  • Angiotensin receptor blockers combined with ACE inhibitors: similar risk of enhanced bradykinin effects.

Moderate Interactions (Monitor Closely)

  • Estrogen‑containing contraceptives: may affect bradykinin metabolism, requiring observation.
  • Neprilysin inhibitors: potential additive effect on bradykinin levels.
  • Other B2 receptor antagonists: may lead to reduced efficacy or unpredictable pharmacodynamics.

Frequently Asked Questions

Icatibant Ethypharm is used to treat acute attacks of hereditary angioedema (HAE) in patients with type I or type II disease. By blocking the bradykinin B2 receptor, it helps reduce swelling and discomfort during an HAE episode.

Icatibant works as a selective antagonist of the bradykinin B2 receptor. By preventing bradykinin from binding, it stops the cascade that leads to vasodilation and increased vascular permeability, thereby limiting the swelling that characterises HAE attacks.

The dose of icatibant is determined by the prescribing clinician based on the patient’s condition and clinical guidelines. Typically, a single subcutaneous injection is administered at the onset of an HAE attack, with additional doses considered only under medical supervision.

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

To order, 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 where needed) and any required import documentation.

Icatibant is a bradykinin B2 receptor antagonist, whereas other HAE therapies such as C1‑esterase inhibitor concentrates replace the deficient protein. Icatibant offers a rapid, subcutaneous option focused on blocking bradykinin, while C1‑esterase inhibitors act upstream in the complement pathway.

Icatibant 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. If temporary storage at room temperature is unavoidable, limit exposure to less than 24 hours.

Icatibant is given as a subcutaneous injection, usually into the abdomen or thigh. The injection is performed by a trained healthcare professional or, after proper instruction, by the patient or caregiver at the onset of an HAE attack.

The most serious risks include severe allergic reactions such as anaphylaxis, unexpected angioedema, and hypotension. Patients should be monitored after injection, and any signs of severe hypersensitivity require immediate medical attention.

Icatibant should not be used by individuals with a known hypersensitivity to icatibant or any of its excipients. Caution is also advised for patients receiving ACE inhibitors or other drugs that increase bradykinin levels, as the risk of angioedema may be heightened.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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