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

Icatibant Auxilia

Active Ingredient:
Icatibant Acetate
Origin:
EU

Icatibant Auxilia (Icatibant Acetate)

Icatibant, the active ingredient in Icatibant Auxilia, is a bradykinin B2 receptor antagonist presented as an injection solution for subcutaneous use. It treats acute attacks of hereditary angioedema in patients with C1‑inhibitor deficiency.

GNH India supplies Icatibant Auxilia as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Auxilia Pharma

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Indications & Clinical Uses

  • Icatibant acts on the bradykinin pathway to manage hereditary angioedema attacks.
  • Acute hereditary angioedema (C1‑inhibitor deficiency): rapid reduction of swelling and pain.
  • Hereditary angioedema type I: blocks bradykinin‑mediated vasodilation.
  • Hereditary angioedema type II: decreases vascular permeability.

How It Works

  • Icatibant is a selective competitive antagonist of the bradykinin B2 receptor. By binding to this receptor, it prevents bradykinin from inducing vasodilation and increasing vascular permeability, thereby limiting the plasma leakage and tissue swelling that characterize acute 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 site of subcutaneous administration.
  • Redness or erythema: localized skin irritation.
  • Swelling at injection site: mild edema around the needle entry.
  • Nausea: transient gastrointestinal upset.
  • Headache: mild to moderate intensity.
  • Dizziness: temporary light‑headedness.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Severe hypotension: marked drop in blood pressure.
  • Angioedema of other regions: swelling beyond the treated area.
  • Urticaria: widespread hives.
  • Thrombocytopenia: low platelet count.
  • Severe allergic reaction: includes bronchospasm or laryngeal edema.

Precautions & Warnings

  • Before using Icatibant, consider the following safety measures.
  • Pregnancy: safety not established; use only if benefit outweighs risk.
  • Breastfeeding: unknown safety; evaluate potential risks.
  • Renal impairment: use with caution; monitor renal function.
  • Concomitant ACE inhibitors: monitor for increased bradykinin‑related effects.
  • History of hypersensitivity: avoid if previous reaction to icatibant.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Icatibant can interact with other medications that influence the bradykinin system or cardiovascular function.

Major Interactions (Avoid)

  • ACE inhibitors: additive bradykinin effect may increase angioedema risk.
  • Angiotensin receptor blockers: similar risk of enhanced bradykinin activity.
  • Other bradykinin B2 antagonists: no additive benefit and may raise adverse‑event likelihood.

Moderate Interactions (Monitor Closely)

  • Diuretics: monitor blood pressure for additive hypotensive effect.
  • NSAIDs: may increase risk of edema.
  • Estrogen‑containing contraceptives: may affect frequency of HAE attacks.

Frequently Asked Questions

Icatibant Auxilia is used to treat acute attacks of hereditary angioedema (HAE) caused by C1‑inhibitor deficiency. It works by rapidly reducing swelling and pain associated with these episodes, providing symptom relief for patients experiencing sudden HAE attacks.

Icatibant is a selective competitive antagonist of the bradykinin B2 receptor. By blocking this receptor, it prevents bradykinin‑mediated vasodilation and increased vascular permeability, which are the primary mechanisms that cause the swelling seen in hereditary angioedema attacks.

The dose of icatibant is determined by the prescribing healthcare professional based on the patient’s clinical condition and regulatory guidelines. The prescriber will decide the appropriate amount and frequency for each individual case.

The safety of icatibant in pregnancy and while breastfeeding has not been established. It should only be used if the potential benefit justifies any possible risk to the fetus or infant, and the decision should be made by a qualified healthcare provider.

To order, submit an enquiry on the product page at gnhindia.com specifying 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 where required) and necessary import documentation.

Icatibant is a bradykinin B2 receptor antagonist, whereas other approved HAE therapies include C1‑inhibitor concentrates and kallikrein inhibitors. Icatibant works by directly blocking bradykinin effects, offering a rapid subcutaneous option, while C1‑inhibitor products replace the deficient protein and are administered intravenously.

Icatibant should be stored at 2‑8 °C (refrigerated). Keep the product in its original packaging, protect it from light, and do not freeze or shake the vial. If temporary temperature excursions occur, follow the manufacturer’s guidance before use.

Icatibant is supplied as a sterile injection solution for subcutaneous use. The medication is injected into the subcutaneous tissue, typically in the abdomen or thigh, by a trained healthcare professional or a patient who has been instructed on proper technique.

The most serious risks include severe allergic reactions such as anaphylaxis, marked hypotension, and systemic angioedema affecting areas other than the treated site. Patients should be monitored for these rare but potentially life‑threatening events and seek immediate medical attention if they occur.

Icatibant should not be used by individuals with a known hypersensitivity to icatibant or any of its excipients. Caution is also advised for patients taking ACE inhibitors or ARBs, and those with uncontrolled cardiovascular conditions should be evaluated before use.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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