GNH USA

Europe — EMA

Icatibant Universal Farma

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

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 treats acute attacks of hereditary angioedema in adults, including type I and type II forms of the disease.

GNH USA supplies Icatibant Universal Farma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

What is Icatibant used for?

Icatibant is a targeted therapy for hereditary angioedema, acting on the bradykinin pathway to relieve swelling.

- Acute hereditary angioedema attacks: rapid reduction of swelling and pain in adults. - Hereditary angioedema type I: alleviates attack‑related edema when administered promptly. - Hereditary angioedema type II: provides fast symptom control during acute episodes.

What are the side effects of Icatibant?

Icatibant may cause a range of adverse reactions, most of which are mild and transient.

Common Side Effects: - Injection site pain: discomfort at the site of subcutaneous injection. - Redness or erythema: localized skin irritation. - Swelling at injection site: mild edema around the needle entry. - Nausea: occasional gastrointestinal upset. - Headache: mild to moderate head discomfort. - Dizziness: transient light‑headedness.

Serious or Rare Side Effects: - Hypersensitivity reactions: rash, itching, or hives. - Anaphylaxis: severe allergic response requiring immediate medical attention. - Severe hypotension: marked drop in blood pressure. - Worsening angioedema: paradoxical increase in swelling. - Infection at injection site: signs of local infection. - Thrombocytopenia: low platelet count observed in rare cases.

What precautions apply to Icatibant?

Before using Icatibant, consider the following safety measures.

- Pregnancy: safety not established; use only if benefit outweighs potential risk. - Breastfeeding: unknown effects; weigh risks and benefits before administration. - Renal impairment: exercise caution and monitor renal function. - Concomitant ACE inhibitors: monitor for increased bradykinin‑related angioedema. - Known 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 that influence bradykinin levels or blood pressure.

Major Interactions (Avoid): - ACE inhibitors: may increase bradykinin, raising risk of angioedema. - Angiotensin receptor blockers: similar potential to elevate bradykinin. - Other bradykinin B2 antagonists: additive pharmacologic effect.

Moderate Interactions (Monitor Closely): - Diuretics: monitor blood pressure and electrolyte balance. - NSAIDs: may exacerbate edema or affect renal function. - Estrogen‑containing contraceptives: possible influence on HAE severity. - Antihistamines: may mask early signs of hypersensitivity. - Corticosteroids: monitor for overlapping immunomodulatory effects.

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 adult patients. It works by rapidly reducing swelling and associated pain during HAE episodes, providing prompt symptom relief.
How does icatibant work in the body?+
Icatibant is a selective antagonist of the bradykinin B2 receptor. By blocking this receptor, it prevents bradykinin‑mediated vasodilation and increased vascular permeability, which are the primary mechanisms causing the swelling seen in hereditary angioedema.
What is the usual dose of icatibant?+
The dose of icatibant is determined by the prescribing healthcare professional based on the patient’s clinical condition and regulatory guidelines. The prescriber will decide the exact amount and frequency of administration for each individual.
Is icatibant safe to use during pregnancy or breastfeeding?+
Safety data for icatibant in pregnancy and lactation are limited. It should only be used if the potential benefit justifies any possible risk to the fetus or infant, and the decision should be made by a qualified healthcare provider.
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 if needed) and import documentation.
How does icatibant compare with other HAE treatments?+
Icatibant is a bradykinin B2 receptor antagonist, whereas other approved HAE therapies include C1‑esterase inhibitor concentrates and kallikrein inhibitors. Icatibant is administered subcutaneously and acts directly at the receptor level, offering rapid symptom control without the need for intravenous infusion.
What are the storage and handling requirements for icatibant?+
Icatibant should be stored at 2‑8 °C in a refrigerator, protected from light. Do not freeze or shake the vial. If temporary temperature excursions occur, consult the product label for guidance before use.
How is icatibant administered?+
Icatibant is given as a subcutaneous injection into the abdomen or thigh. The injection is performed by a trained healthcare professional or, in some cases, by the patient after proper instruction. The site should be rotated for repeated doses.
What are the most serious risks associated with icatibant?+
Serious risks include hypersensitivity reactions such as anaphylaxis, severe hypotension, and paradoxical worsening of angioedema. Patients should be monitored closely after administration, and any signs of severe allergic reaction require immediate medical attention.
Who should not use icatibant?+
Icatibant is contraindicated in patients with known hypersensitivity to icatibant or any of its excipients. Caution is also advised for individuals with severe renal impairment or those taking 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
Universal Farma, S.L.
Origin
EU

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