GNH USA

Europe — EMA

Icatibant Glenmark

GNH USA supplies Icatibant Glenmark (Icatibant), a bradykinin B2 receptor antagonist for acute attacks of hereditary angioedema.

Icatibant

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What is Icatibant?

Icatibant, the active ingredient in Icatibant Glenmark, is a bradykinin B2 receptor antagonist presented as a 30 mg per 0.3 mL prefilled syringe solution for subcutaneous use. It is indicated for the treatment of acute attacks of hereditary angioedema in patients with C1‑inhibitor deficiency.

GNH USA supplies Icatibant Glenmark as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with distribution across EU and other regulated markets.

What is Icatibant used for?

Icatibant is used to manage hereditary angioedema by blocking the bradykinin pathway.

Hereditary angioedema (C1‑inhibitor deficiency): provides rapid reduction of swelling during acute attacks. Hereditary angioedema (type I/II): alleviates edema and associated pain when an attack occurs. Hereditary angioedema (type III/normal C1‑inhibitor): can be employed for acute symptom control in regions where approved.

What are the side effects of Icatibant?

The most frequently reported reactions to icatibant are related to the injection site, while rare events may involve systemic hypersensitivity.

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

Serious or Rare Side Effects: - Anaphylaxis: severe allergic reaction requiring immediate medical attention. - Angioedema of the face or airway: potentially life‑threatening swelling. - Hypotension: sudden drop in blood pressure, may cause dizziness.

What precautions apply to Icatibant?

When prescribing icatibant, clinicians should consider several safety and handling factors.

Pregnancy: safety not established; use only if potential benefit justifies the risk. Breastfeeding: unknown excretion; weigh benefits against possible infant exposure. Renal impairment: no dose adjustment required, but monitor for accumulation. Concomitant ACE inhibitors or ARBs: may increase risk of angioedema; observe closely. Hypersensitivity: discontinue treatment if signs of allergic reaction appear. Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Icatibant interact with?

Icatibant may interact with other agents that influence the bradykinin system or fluid balance.

Major Interactions (Avoid): - ACE inhibitors: combined use can heighten the risk of angioedema. - Concurrent use of ARBs with ACE inhibitors: avoid due to additive bradykinin effects.

Moderate Interactions (Monitor Closely): - Estrogen‑containing oral contraceptives: may exacerbate hereditary angioedema; monitor symptoms. - Diuretics: can affect plasma volume; observe for changes in edema. - Other bradykinin‑targeting therapies (e.g., ecallantide): monitor for additive effects on blood pressure and swelling.

Frequently asked questions

What is Icatibant Glenmark used for?+
Icatibant Glenmark is indicated for the treatment of acute attacks of hereditary angioedema (HAE) in patients who have a deficiency of C1‑inhibitor. By rapidly reducing swelling, it helps restore normal airway function and alleviates pain associated with HAE episodes.
How does icatibant work?+
Icatibant works as 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 that cause the swelling seen in hereditary angioedema.
What is the usual dose of icatibant?+
The prescribed dose of icatibant is determined by the treating physician. The product is supplied as a 30 mg/0.3 mL prefilled syringe for subcutaneous injection, and the prescriber decides the timing and number of injections based on the severity of the HAE attack.
Is icatibant safe in pregnancy or breastfeeding?+
Safety data for icatibant during pregnancy and lactation are limited. It is classified as pregnancy category unknown, so it should only be used when the potential benefit outweighs any possible risk to the fetus or infant. Breastfeeding mothers should discuss potential exposure with their healthcare provider.
How do I order Icatibant Glenmark from GNH USA?+
To place an order, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA supplies hospitals, pharmacies and procurement teams worldwide, and will request trade or institutional credentials before providing pricing, availability, shipping details (including cold‑chain handling) and import documentation.
How does icatibant compare with the main alternative therapy for HAE?+
The primary alternative for acute HAE attacks is plasma‑derived or recombinant C1‑inhibitor concentrate. Icatibant directly blocks the bradykinin B2 receptor, offering a rapid subcutaneous option, whereas C1‑inhibitor replacement works by restoring the deficient protein and is administered intravenously. Choice depends on patient preference, attack severity and clinical guidelines.
How should Icatibant be stored and handled?+
Icatibant should be stored at 2‑8 °C (refrigerated). Keep the prefilled syringes in their original packaging, protect them from light, and do not freeze or shake the product. If a temporary temperature excursion occurs, consult the manufacturer’s stability guidelines before use.
How is Icatibant administered?+
Icatibant is given as a single subcutaneous injection using the prefilled 0.3 mL syringe. The injection site is typically the abdomen or thigh. Patients or caregivers should follow aseptic technique, rotate injection sites, and monitor for any immediate reactions after administration.
What are the most serious risks to watch for with icatibant?+
The most serious adverse events include anaphylaxis, severe angioedema of the face or airway, and sudden hypotension. Any signs of difficulty breathing, swelling of the lips or tongue, or a rapid drop in blood pressure require immediate medical attention and discontinuation of the drug.
Who should not use icatibant?+
Icatibant is contraindicated in individuals with a known hypersensitivity to icatibant or any of its excipients. Caution is also advised for patients with a history of severe allergic reactions, uncontrolled cardiovascular disease, or those receiving ACE inhibitors or ARBs without appropriate monitoring.
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
Glenmark Arzneimittel Gmbh
Origin
EU

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