GNH USA

Europe — EMA

Icatibant "viatris"

GNH USA supplies Icatibant viatris (Icatibant), a bradykinin B2 receptor antagonist for hereditary angioedema attacks. Request a quote for global supply.

Icatibant

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What is Icatibant?

Icatibant, the active ingredient in Icatibant viatris, is a bradykinin B2 receptor antagonist presented as a sterile subcutaneous injection solution for subcutaneous use. It is indicated for the treatment of acute hereditary angioedema attacks in patients with confirmed HAE diagnosis and can provide rapid symptom relief under medical supervision.

GNH USA supplies Icatibant viatris as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with a focus on quality assurance, regulatory compliance and reliable cold‑chain logistics for biologic products across Europe, Asia and the Americas.

What is Icatibant used for?

Icatibant is used to target bradykinin‑mediated pathways in hereditary angioedema, providing rapid control of swelling.

- Hereditary angioedema type I: reduces swelling during acute attacks, improving airway safety. - Hereditary angioedema type II: provides rapid symptom control and shortens attack duration. - Hereditary angioedema with normal C1‑INH: offers targeted therapy for patients unresponsive to C1‑INH replacement. - Acute HAE attacks in adults: delivers a subcutaneous dose that quickly alleviates pain and edema.

What are the side effects of Icatibant?

Icatibant may cause a range of adverse reactions, most of which are related to the injection site or systemic response.

Common Side Effects: - Injection site pain: mild to moderate discomfort at the injection site. - Redness: localized erythema around the injection area. - Nausea: occasional feeling of queasiness.

Serious or Rare Side Effects: - Anaphylaxis: severe allergic reaction requiring immediate medical attention. - Angioedema: worsening of swelling in face, lips or airway. - Severe hypotension: sudden drop in blood pressure.

What precautions apply to Icatibant?

Before using Icatibant, consider the following precautions: - Pregnancy: safety not established; use only if benefit outweighs risk. - Breastfeeding: unknown effects; consider discontinuation. - Renal impairment: use with caution, monitor patient response. - Concomitant ACE inhibitors: increased risk of bradykinin‑mediated angioedema; monitor closely. - Hypersensitivity: discontinue immediately if allergic reaction occurs. - 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; review the following categories.

Major Interactions (Avoid): - ACE inhibitors: may potentiate bradykinin accumulation and increase risk of angioedema. - Estrogen‑containing contraceptives: can exacerbate bradykinin‑mediated swelling.

Moderate Interactions (Monitor Closely): - NSAIDs: may augment inflammatory response, monitor for increased edema. - C1‑INH concentrate: concurrent use may reduce efficacy of Icatibant; assess clinical need. - Other bradykinin antagonists: additive pharmacodynamic effect; adjust therapy as needed.

Frequently asked questions

What is Icatibant used for?+
Icatibant is indicated for the treatment of acute hereditary angioedema (HAE) attacks. It works by rapidly reducing swelling caused by excess bradykinin, helping to relieve symptoms such as facial, peripheral, or airway edema in patients with confirmed HAE.
How does Icatibant work?+
Icatibant is a competitive antagonist of the bradykinin B2 receptor. By binding to this receptor on vascular endothelial cells, it blocks bradykinin‑induced vasodilation and increased vascular permeability, thereby preventing the fluid leakage that causes swelling during HAE attacks.
What is the usual dose of Icatibant?+
The dose of Icatibant is determined by the prescribing healthcare professional based on the patient’s condition and clinical guidelines. The prescriber decides the amount, frequency, and duration of therapy, and patients should follow the exact instructions provided on the prescription label.
Is Icatibant safe in pregnancy or breastfeeding?+
Safety data for Icatibant in pregnancy and lactation are limited. The product is classified as having an unknown pregnancy category, and its use is generally reserved for situations where the potential benefit justifies any potential risk. Breastfeeding mothers should discuss risks with their physician.
How do I order Icatibant viatris from GNH USA?+
To order Icatibant viatris, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain handling), and necessary import documentation.
How does Icatibant compare with the main alternative treatment for HAE?+
The primary alternative for HAE is C1‑esterase inhibitor (C1‑INH) concentrate, which replaces the deficient protein. Icatibant, by contrast, blocks the downstream bradykinin B2 receptor, offering a rapid, subcutaneous option that does not require intravenous infusion. Choice of therapy depends on patient preference, attack severity, and clinical response.
What are the storage and handling requirements for Icatibant?+
Icatibant should be stored refrigerated at 2‑8 °C. Keep the product in its original packaging, protect it from light, and avoid freezing or shaking the vial. If temporary temperature excursions occur, consult the product’s stability guidelines before use.
How is Icatibant administered?+
Icatibant is supplied as a sterile solution for subcutaneous injection. The prescribed dose is injected into the subcutaneous tissue of the abdomen, thigh, or upper arm using the pre‑filled syringe or autoinjector provided. Patients should be instructed on proper injection technique and site rotation.
What are the most serious risks associated with Icatibant?+
The most serious adverse reactions include anaphylaxis, severe angioedema involving the airway, and sudden hypotension. These events require immediate medical attention. Patients should be monitored after the first dose and instructed to seek emergency care if they experience any signs of a severe allergic reaction.
Who should not use Icatibant?+
Icatibant is contraindicated in individuals with known hypersensitivity to the active substance or any of the excipients in the formulation. Patients with a history of severe allergic reactions to bradykinin antagonists should avoid its use, and clinicians should assess risk before prescribing.
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
Viatris Limited
Origin
EU

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