GNH USA

Europe — EMA

Icatibant Sun

GNH USA supplies Icatibant Sun (icatibant), a bradykinin B2 receptor antagonist for acute hereditary angioedema attacks in adults. Request a quote globally.

Icatibant

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What is 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 USA 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.

What is Icatibant used for?

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.

What are the side effects of Icatibant?

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.

What precautions apply to Icatibant?

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.

What does Icatibant interact with?

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

What is Icatibant Sun used for?+
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.
How does icatibant work?+
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.
What is the usual dose of Icatibant Sun?+
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.
Is Icatibant Sun safe during pregnancy or breastfeeding?+
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.
How do I order Icatibant Sun from GNH USA?+
To order Icatibant Sun, submit an enquiry on the product page at gnh-usa.com with the required quantity. GNH USA 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.
How does Icatibant compare with the main alternative drug for HAE?+
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.
What are the storage and handling requirements for Icatibant Sun?+
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.
How is Icatibant Sun administered?+
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.
What are the most serious risks to watch for when using Icatibant Sun?+
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.
Who should not use Icatibant Sun?+
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.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Icatibant
Route
Subcutaneous Use
Manufacturer
Sun Pharmaceutical Industries Europe B.V.
Origin
EU

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