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

Icatibant Sun

Active Ingredient:
Icatibant
Origin:
EU

Icatibant Sun (Icatibant)

Icatibant, the active ingredient in Icatibant Sun, is a bradykinin B2 receptor antagonist presented as a sterile solution for subcutaneous injection use. It is indicated for the treatment of acute attacks of hereditary angioedema in adult patients, providing rapid symptom relief by blocking bradykinin‑mediated vascular effects.

GNH India supplies Icatibant Sun as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring quality‑assured products that meet European Union regulatory standards through a robust cold‑chain logistics network and dedicated regulatory support.

Manufacturer / TM Owner

Sun Pharmaceutical Industries Europe B.V.

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Indications & Clinical Uses

  • Icatibant is a bradykinin B2 receptor antagonist used in the management of hereditary angioedema.
  • Hereditary angioedema (HAE) acute attacks: rapid reduction of swelling and associated pain in adult patients.

How It Works

  • Icatibant selectively and competitively binds to the bradykinin B2 receptor on vascular endothelial cells, preventing bradykinin from activating the receptor. By blocking this pathway, it inhibits bradykinin‑induced vasodilation, increased vascular permeability, and subsequent plasma extravasation that cause the characteristic swelling of hereditary angioedema. The antagonism is rapid, allowing prompt reversal of acute edema episodes in patients and improves quality of life.

Side Effects

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

Common Side Effects

  • Injection site pain: mild to moderate discomfort at the injection site.
  • Injection site erythema: redness around the injection area.
  • Injection site swelling: localized edema.
  • Nausea: occasional feeling of queasiness.
  • Headache: transient head pain.
  • Dizziness: light‑headed sensation.

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 throat: swelling that may compromise airway.
  • Urticaria: widespread hives.
  • Thrombocytopenia: low platelet count.
  • Severe injection site reaction: necrosis or extensive tissue damage.

Precautions & Warnings

Before using Icatibant, consider the following precautions to ensure safe administration.

  • Hypersensitivity assessment: verify no known allergy to icatibant or any formulation components.
  • Cardiovascular monitoring: observe patients with existing heart disease for blood pressure changes.
  • Pregnancy and lactation: safety has not been established; use only if the potential benefit justifies the risk.
  • Concomitant bradykinin‑modulating drugs: avoid combining with other B2 receptor antagonists.
  • Renal or hepatic impairment: dose adjustment is not established; monitor clinical response.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Icatibant can interact with other medicines; awareness of major and moderate interactions helps prevent adverse outcomes.

Major Interactions (Avoid)

  • ACE inhibitors: may increase bradykinin levels and reduce icatibant efficacy.
  • Neprilysin inhibitors (e.g., sacubitril): elevate bradykinin, potentially diminishing therapeutic effect.
  • Estrogen‑containing therapies: can exacerbate hereditary angioedema severity.
  • Other bradykinin B2 receptor antagonists: additive antagonism may lead to unexpected effects.
  • Immunosuppressants that alter immune response: may affect injection site reactions.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may increase risk of gastrointestinal discomfort.
  • Diuretics: monitor blood pressure and electrolyte balance.
  • Corticosteroids: observe for enhanced immunosuppression.
  • Antihistamines: may mask early signs of allergic reactions.
  • Anticoagulants: watch for bleeding at injection sites.

Frequently Asked Questions

Icatibant Sun is indicated for the treatment of acute attacks of hereditary angioedema (HAE) in adult patients. It works by rapidly reducing swelling and associated pain during an HAE episode.

Icatibant selectively blocks the bradykinin B2 receptor on vascular endothelial cells, preventing bradykinin‑induced vasodilation and increased vascular permeability. This inhibition stops the plasma leakage that causes the swelling seen in hereditary angioedema.

The dosing regimen for Icatibant Sun is determined by the prescribing healthcare professional based on the patient’s clinical condition and regulatory guidelines. Patients should follow the prescriber’s instructions exactly.

Safety data for Icatibant Sun in pregnancy and lactation are limited. It should be used only if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and under medical supervision.

To order Icatibant Sun, 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 where required) and import documentation.

The primary alternative for acute HAE attacks is a C1‑esterase inhibitor (e.g., Berinert). While C1‑esterase inhibitors replace the deficient protein, icatibant directly blocks the bradykinin B2 receptor. Icatibant offers a subcutaneous route and rapid onset, whereas C1‑esterase inhibitors are administered intravenously.

Icatibant Sun 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 before use.

Icatibant Sun is supplied as a sterile solution for subcutaneous injection. The prescribed dose is injected into the subcutaneous tissue, typically in the abdomen or thigh, using the supplied pre‑filled syringe or auto‑injector as directed by the healthcare provider.

Serious risks include anaphylaxis, severe hypotension, angioedema of the face or throat that could compromise the airway, urticaria, and thrombocytopenia. Patients should seek immediate medical attention if any of these symptoms develop.

Icatibant Sun should not be used by individuals with a known hypersensitivity to icatibant or any component of the formulation. Caution is also advised in patients receiving other bradykinin‑modulating therapies or those with uncontrolled cardiovascular disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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