GNH USA

Europe — EMA

Icatibant Universal Farma

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

Icatibant

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What is Icatibant?

Icatibant, the active ingredient in Icatibant Universal Farma, is a bradykinin B2 receptor antagonist presented as a solution for subcutaneous injection use. It treats hereditary angioedema in patients with C1‑inhibitor deficiency, reducing swelling episodes caused by excess bradykinin.

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 used to manage hereditary angioedema, a disorder involving excessive bradykinin activity.

- Hereditary angioedema (type I & II, C1‑inhibitor deficiency): Reduces the frequency and severity of swelling attacks by blocking the B2 receptor. - Hereditary angioedema (type III, normal C1‑inhibitor): Provides rapid relief of acute edema through bradykinin antagonism. - Acute attacks of hereditary angioedema: Offers prompt symptom control when administered at the onset of swelling.

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 exposure.

Common Side Effects: - Injection site pain: mild to moderate discomfort at the injection site. - Redness or erythema: localized skin flushing. - Swelling at injection site: transient localized edema. - Nausea: occasional gastrointestinal upset. - Headache: mild to moderate intensity. - Dizziness: transient light‑headedness.

Serious or Rare Side Effects: - Anaphylaxis: severe allergic reaction requiring immediate medical attention. - Severe hypotension: marked drop in blood pressure. - Urticaria: widespread hives. - Angioedema unrelated to HAE: unexpected swelling in other areas. - Thrombocytopenia: low platelet count observed in rare cases. - Severe allergic reaction: includes bronchospasm or facial swelling.

What precautions apply to Icatibant?

Before using Icatibant, consider the following safety measures.

- Pregnancy: safety not established; use only if potential benefit justifies the risk. - Breastfeeding: unknown excretion; weigh benefits against possible infant exposure. - Renal impairment: exercise caution; monitor renal function as clearance may be affected. - Concomitant ACE inhibitors: may increase bradykinin levels; observe for enhanced angioedema. - Hypersensitivity: discontinue immediately if signs of severe allergic reaction appear. - 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 pathways or fluid balance.

Major Interactions (Avoid): - ACE inhibitors: additive bradykinin effect may worsen angioedema. - Other bradykinin‑targeting biologics: may reduce therapeutic efficacy.

Moderate Interactions (Monitor Closely): - NSAIDs: may increase risk of swelling or gastrointestinal irritation. - Estrogen‑containing contraceptives: can exacerbate hereditary angioedema attacks. - Diuretics: may alter fluid status and affect edema management.

Frequently asked questions

What is Icatibant Universal Farma used for?+
Icatibant Universal Farma is indicated for the treatment of hereditary angioedema (HAE) attacks in patients with C1‑inhibitor deficiency. By blocking the bradykinin B2 receptor, it helps to rapidly reduce swelling associated with acute HAE episodes.
How does icatibant work?+
Icatibant is a selective antagonist of the bradykinin B2 receptor. It binds to this receptor on vascular endothelial cells, preventing bradykinin from triggering vasodilation and increased vascular permeability, which are the primary mechanisms behind angioedema swelling.
What is the usual dose of icatibant?+
The dose of Icatibant Universal Farma is determined by the prescribing clinician based on the patient’s condition, severity of the attack, and clinical guidelines. Healthcare professionals set the exact amount and frequency of administration.
Is icatibant safe during pregnancy or breastfeeding?+
Safety data for icatibant in pregnancy and lactation are limited. It should only be used if the potential benefit justifies the potential 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 where required) 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‑inhibitor concentrates and kallikrein inhibitors. Icatibant provides a rapid, subcutaneous option focused on blocking bradykinin, while C1‑inhibitor products replace the deficient protein and kallikrein inhibitors target upstream pathways.
What are the storage and handling requirements for icatibant?+
Icatibant Universal Farma should be stored at 2‑8 °C (refrigerated). Keep the vial in its original packaging, protect it from light, and avoid freezing or shaking the solution. If temporary temperature excursions occur, consult the product label before use.
How is icatibant administered?+
Icatibant is supplied as a solution for subcutaneous injection. The prescribed dose is injected into the subcutaneous tissue, typically in the abdomen or thigh, using a sterile needle. Administration is performed by the patient or a trained caregiver under medical guidance.
What are the most serious risks associated with icatibant?+
The most serious risks include anaphylaxis, severe hypotension, and rare cases of thrombocytopenia. Patients should be monitored for signs of severe allergic reaction, sudden drop in blood pressure, or unexplained bleeding, and seek immediate medical attention if these occur.
Who should not use icatibant?+
Icatibant is contraindicated in individuals with known hypersensitivity to icatibant or any of its excipients. Patients with a history of severe allergic reactions to the drug should avoid its use, and clinicians should assess each patient’s medical history 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
Universal Farma, S.L.
Origin
EU

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