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

Icatibant

Active Ingredient:
Icatibant Acetate
Origin:
EU

Icatibant (Icatibant Acetate)

Icatibant, the active ingredient in Icatibant, is a bradykinin B2 receptor antagonist presented as an injectable solution for subcutaneous administration. It is indicated for the treatment of acute attacks of hereditary angioedema in patients who have a C1‑inhibitor deficiency, helping to reduce swelling and related symptoms.

GNH India supplies Icatibant as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with distribution aligned to EU regulatory standards.

Manufacturer / TM Owner

Newbury Pharmaceuticals Ab

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Indications & Clinical Uses

Icatibant acts on the bradykinin pathway to control hereditary angioedema episodes.

  • Hereditary angioedema (C1‑inhibitor deficiency): rapidly reduces swelling during acute attacks.
  • Hereditary angioedema type I: provides prompt symptom relief.
  • Hereditary angioedema type II: blocks bradykinin‑mediated edema.
  • Acute angioedema not responding to C1‑inhibitor therapy: offers an alternative mechanism of action.

How It Works

  • Icatibant is a selective antagonist of the bradykinin B2 receptor. By binding to this receptor, it blocks the actions of bradykinin, preventing the vasodilation and increased vascular permeability that lead to the 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 exposure.

Common Side Effects

  • Injection site pain: discomfort at the subcutaneous injection site.
  • Injection site erythema: redness around the injection area.
  • Injection site swelling: localized edema.
  • Nausea: feeling of stomach upset.
  • Headache: mild to moderate head pain.
  • Dizziness: transient sense of light‑headedness.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Severe hypotension: marked drop in blood pressure.
  • Angioedema of the face or airway: swelling that can compromise breathing.
  • Urticaria: widespread hives.
  • Infection at injection site: signs of local infection.
  • Thrombocytopenia: low platelet count observed in rare cases.

Precautions & Warnings

Before using icatibant, several safety considerations should be observed.

  • Confirm diagnosis: verify hereditary angioedema with C1‑inhibitor deficiency.
  • Assess hypersensitivity: monitor for allergic reactions to icatibant or excipients.
  • Administer under supervision: ensure trained healthcare personnel give the subcutaneous injection.
  • Avoid in known hypersensitivity: do not use if the patient has a documented allergy to icatibant.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Icatibant can interact with other medicines that affect the bradykinin system or blood pressure.

Major Interactions (Avoid)

  • ACE inhibitors: may increase bradykinin levels and raise the risk of angioedema.
  • Angiotensin receptor blockers: similar potential to elevate bradykinin‑related swelling.
  • Other bradykinin B2 antagonists: additive pharmacologic effect may be unsafe.

Moderate Interactions (Monitor Closely)

  • Estrogen‑containing contraceptives: may influence hereditary angioedema severity.
  • C1‑inhibitor concentrate: concurrent use may be unnecessary and should be coordinated.
  • Diuretics: monitor blood pressure changes when combined with icatibant.

Frequently Asked Questions

Icatibant is used to treat acute attacks of hereditary angioedema in patients who have a C1‑inhibitor deficiency. It works by rapidly reducing swelling and related symptoms during an HAE episode.

Icatibant selectively blocks the bradykinin B2 receptor, preventing bradykinin from causing vasodilation and increased vascular permeability. This inhibition stops the swelling process that characterises hereditary angioedema attacks.

The dose of Icatibant is determined by the prescribing healthcare professional based on the patient’s condition and regulatory guidelines. Patients should follow the exact dosing instructions provided by their prescriber.

The safety of Icatibant in pregnancy or while breastfeeding has not been fully established. Healthcare providers should weigh the potential benefits against any possible risks before prescribing it to pregnant or nursing individuals.

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

Icatibant differs from C1‑inhibitor concentrates by targeting the bradykinin pathway directly rather than replacing the deficient protein. This provides a rapid, subcutaneous option for patients who may not respond adequately to protein‑based therapies.

Icatibant should be stored at 2‑8 °C in a refrigerator, protected from light. Do not freeze or shake the vial. Keep it in the original packaging until use to maintain stability.

Icatibant is given as a single subcutaneous injection, typically into the abdomen or thigh. The injection should be performed by a trained healthcare professional using aseptic technique.

The most serious risks include anaphylaxis, severe hypotension, and airway‑compromising angioedema. Patients should be monitored closely after injection and seek immediate medical attention if any of these symptoms develop.

Icatibant should not be used in individuals with known hypersensitivity to the drug or any of its excipients. It is also contraindicated in patients who have experienced severe allergic reactions to other bradykinin B2 antagonists.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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