GNH USA

Europe — EMA

Icatibant Universal Farma

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

Icatibant

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What is Icatibant?

Icatibant, the active ingredient in Icatibant Universal Farma, is a bradykinin B2 receptor antagonist presented as an injection solution for subcutaneous use. It is indicated for the treatment of acute attacks of hereditary angioedema in patients with C1‑inhibitor deficiency, providing rapid reduction of swelling and associated discomfort.

GNH USA supplies Icatibant Universal Farma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with a focus on quality assurance and regulatory compliance and timely delivery to global markets.

What is Icatibant used for?

Icatibant acts on the bradykinin pathway to relieve hereditary angioedema symptoms.

- Hereditary angioedema type I: rapid reduction of swelling and pain during acute attacks, often within minutes of administration. - Hereditary angioedema type II: alleviates edema and associated discomfort during flare‑ups, helping restore normal function. - Hereditary angioedema with normal C1‑inhibitor: provides effective symptom control during acute episodes, reducing airway and peripheral swelling.

What are the side effects of Icatibant?

Icatibant may cause a range of adverse reactions, most of which are related to its subcutaneous administration.

Common Side Effects: - Injection site pain: mild discomfort. - Redness: localized erythema. - Swelling: transient edema. - Nausea: occasional queasiness. - Headache: mild to moderate. - Dizziness: brief light‑headedness.

Serious or Rare Side Effects: - Hypersensitivity: rash or hives. - Anaphylaxis: severe allergic reaction. - Severe hypotension: sudden blood‑pressure drop. - Paradoxical angioedema: worsening swelling. - Thrombocytopenia: low platelet count. - Urticaria: widespread hives.

What precautions apply to Icatibant?

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

- Allergy assessment: verify no known hypersensitivity to icatibant or formulation components. - Pregnancy: safety not established; use only if potential benefit justifies risk. - Breastfeeding: unknown excretion; weigh benefits against possible infant exposure. - Renal impairment: no dosage adjustment required, but monitor for accumulation of adverse effects. - 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 that influence bradykinin levels or vascular tone.

Major Interactions (Avoid): - ACE inhibitors: may increase bradykinin and exacerbate angioedema. - Concomitant B2 receptor antagonists: additive blockade could alter efficacy.

Moderate Interactions (Monitor Closely): - Estrogen‑containing oral contraceptives: may raise attack frequency; monitor symptoms. - NSAIDs: can trigger angioedema in susceptible individuals; observe closely. - C1‑inhibitor concentrate administered simultaneously: may affect therapeutic response; coordinate timing.

Frequently asked questions

What is Icatibant Universal Farma used for?+
Icatibant Universal Farma is indicated for the treatment of acute attacks of hereditary angioedema (HAE) in patients with C1‑inhibitor deficiency. It works to quickly reduce swelling and associated pain during an HAE flare, helping restore normal breathing and facial function.
How does icatibant work?+
Icatibant is a selective antagonist of the bradykinin B2 receptor. By blocking this receptor on vascular endothelial cells, it prevents bradykinin‑induced vasodilation and increased vascular permeability, which are the primary drivers of the rapid swelling seen in hereditary angioedema attacks.
What is the usual dose of icatibant?+
The dosage of icatibant is determined by the prescribing clinician based on the patient’s condition and regulatory guidelines. Typically, a single subcutaneous injection is administered at the onset of an acute HAE attack, with additional doses given only if medically required.
Is icatibant safe in pregnancy or breastfeeding?+
Safety data for icatibant during 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 the decision should be made in consultation with a healthcare professional.
How do I order Icatibant Universal Farma from GNH USA?+
To place an order, 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 if needed) and any required import documentation.
How does icatibant compare with the main alternative treatment for HAE?+
The primary alternative for HAE is plasma‑derived or recombinant C1‑inhibitor concentrate, which replaces the deficient protein. Icatibant, by contrast, blocks the downstream bradykinin B2 receptor. Both provide rapid symptom relief, but icatibant is a small‑molecule injection that does not require plasma sourcing, while C1‑inhibitor products are larger proteins administered intravenously.
What are the storage and handling requirements for icatibant?+
Icatibant should be stored refrigerated at 2‑8 °C. Keep the vial in its original packaging, protect it from light, and do not freeze or shake the solution. If refrigeration is temporarily unavailable, the product may remain at controlled room temperature for a limited period as indicated in the labeling.
How is icatibant given or administered?+
Icatibant is administered as a subcutaneous injection, usually into the abdomen or thigh. The injection can be performed by a healthcare professional or, after proper training, by the patient or caregiver at the onset of an HAE attack. The site should be rotated to minimize local irritation.
What are the most serious risks to watch for when using icatibant?+
Serious risks include hypersensitivity reactions such as rash, hives, or anaphylaxis, as well as severe hypotension and paradoxical worsening of angioedema. Patients should be instructed to seek immediate medical attention if they experience signs of a severe allergic reaction, sudden drop in blood pressure, or unexpected swelling after injection.
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 currently receiving ACE inhibitors or other medications that increase bradykinin levels, as the combination may heighten the risk of angioedema.
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
Universal Farma, S.L.
Origin
EU

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