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

Icatibant Al

Active Ingredient:
Icatibant
Origin:
EU

Icatibant Al (Icatibant)

Icatibant, the active ingredient in Icatibant Al, is a Bradykinin B2 receptor antagonist presented as a solution for injection for subcutaneous use. It treats acute attacks of hereditary angioedema type I and type II in patients with hereditary angioedema.

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

Manufacturer / TM Owner

Aliud Pharma Gmbh

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Indications & Clinical Uses

Icatibant is a selective bradykinin B2 receptor antagonist used to manage hereditary angioedema attacks.

  • Acute attacks of hereditary angioedema type I: provides rapid reduction of swelling and pain.
  • Acute attacks of hereditary angioedema type II: alleviates edema and improves airway patency.
  • Hereditary angioedema (any type): offers prompt symptom control during episodic flare‑ups.

How It Works

  • Icatibant acts as a selective competitive antagonist at the bradykinin B2 receptor. By binding to this receptor, it blocks the actions of bradykinin, preventing vasodilation and increased vascular permeability that underlie the swelling seen in hereditary angioedema. The inhibition of the bradykinin pathway results in rapid resolution of edema during acute attacks.

Side Effects

Icatibant may cause a range of adverse reactions, most of which are mild and transient.

Common Side Effects

  • Injection site pain: discomfort at the subcutaneous injection site.
  • Redness or swelling at injection site: localized erythema.
  • Nausea: mild gastrointestinal upset.
  • Headache: transient cranial discomfort.
  • Dizziness: occasional light‑headedness.
  • Flushing: brief warmth or redness of the skin.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Angioedema unrelated to HAE: unexpected swelling in other body parts.
  • Hypotension: significant drop in blood pressure.
  • Severe injection‑site reactions: necrosis or ulceration.
  • Thrombocytopenia: low platelet count observed in rare cases.

Precautions & Warnings

Before using Icatibant, consider the following safety measures.

  • Pregnancy: safety not established; use only if benefit outweighs potential risk.
  • Breastfeeding: unknown excretion; weigh maternal benefit against infant risk.
  • Renal impairment: no dosage adjustment required, but monitor for accumulation.
  • Concomitant ACE inhibitors or neprilysin inhibitors: may increase bradykinin levels; observe for enhanced edema.
  • Hypersensitivity: discontinue immediately if signs of allergic reaction appear.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Icatibant can interact with other agents that influence the bradykinin pathway or cardiovascular function.

Major Interactions (Avoid)

  • ACE inhibitors: may potentiate bradykinin‑mediated effects, increasing risk of angioedema.
  • Neprilysin inhibitors (e.g., sacubitril): elevate bradykinin levels, heightening adverse‑event potential.
  • Other bradykinin‑potentiating drugs: additive risk of swelling.

Moderate Interactions (Monitor Closely)

  • Diuretics: may affect blood pressure when combined with hypotensive episodes.
  • Antihypertensive agents: monitor for excessive blood pressure reduction.
  • Other subcutaneous biologics: assess injection‑site tolerance when administered concurrently.

Frequently Asked Questions

Icatibant Al is indicated for the treatment of acute attacks of hereditary angioedema (HAE) types I and II. It works by rapidly reducing swelling caused by excess bradykinin, helping to restore normal airway function and relieve discomfort during HAE episodes.

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

The dosage of Icatibant Al is determined by the prescribing healthcare professional based on the patient’s clinical condition and regulatory guidelines. The prescriber will decide the exact amount and frequency of administration for each acute HAE episode.

Safety data for Icatibant in pregnancy and lactation are limited. It should be used only if the potential benefit justifies any possible risk to the fetus or infant. Healthcare providers will evaluate the individual situation before prescribing.

To place an 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 logistics if needed), and import documentation.

Icatibant is a bradykinin B2 receptor antagonist, whereas other approved HAE therapies include C1‑esterase inhibitor concentrates and kallikrein inhibitors. Icatibant offers a subcutaneous route and rapid onset of action, making it convenient for self‑administration during acute attacks.

Icatibant Al 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 to maintain stability and potency.

Icatibant Al is supplied as a sterile solution for subcutaneous injection. The medication is injected into the abdominal wall or thigh using a pre‑filled syringe, following the dosing instructions provided by the prescribing clinician.

The most serious adverse events include anaphylaxis, severe angioedema unrelated to HAE, and significant hypotension. Patients should be monitored for signs of allergic reaction or sudden blood pressure changes after administration and seek immediate medical care if they occur.

Icatibant is contraindicated in individuals with known hypersensitivity to icatibant or any component of the formulation. Caution is also advised for patients receiving ACE inhibitors, neprilysin inhibitors, or other bradykinin‑enhancing agents due to an increased risk of angioedema.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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