GNH USA

Europe — EMA

Icatibant Hikma

GNH USA supplies Icatibant Hikma (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 Hikma, is a Bradykinin B2 receptor antagonist presented as an injection for intravenous use. It treats hereditary angioedema attacks in patients with a confirmed diagnosis.

GNH USA supplies Icatibant Hikma 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 acute swelling.

Hereditary angioedema attacks: provides rapid reduction of edema and associated pain during an acute episode.

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 or erythema - Headache - Nausea or vomiting - Dizziness or light‑headedness - Flushing - Fatigue

Serious or Rare Side Effects: - Severe hypersensitivity or anaphylaxis - Angioedema unrelated to hereditary disease - Urticaria or rash - Significant hypotension - Necrotic skin reactions at injection site - Pulmonary edema

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 effects; weigh benefits against possible infant exposure. - Renal impairment: no specific dose adjustment, but monitor renal function. - Concomitant ACE inhibitors or neprilysin inhibitors: may increase bradykinin levels; observe for enhanced edema. - Known hypersensitivity: discontinue immediately if severe 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 agents that influence bradykinin or vascular tone.

Major Interactions (Avoid): - ACE inhibitors: may potentiate bradykinin‑mediated effects, increasing risk of angioedema. - Neprilysin inhibitors (e.g., sacubitril): elevate bradykinin levels, heightening adverse event potential. - Other bradykinin B2 antagonists: additive pharmacodynamic effects.

Moderate Interactions (Monitor Closely): - NSAIDs: may exacerbate gastrointestinal irritation. - Estrogen‑containing contraceptives: possible increase in bradykinin activity. - Diuretics: monitor blood pressure and electrolyte balance. - Antihistamines: may mask early signs of hypersensitivity. - Corticosteroids: assess for overlapping immunomodulatory effects.

Frequently asked questions

What is Icatibant Hikma used for?+
Icatibant Hikma is indicated for the treatment of acute attacks of hereditary angioedema (HAE) in patients with a confirmed diagnosis. It works to quickly reduce swelling and associated discomfort during an HAE episode.
How does icatibant work?+
Icatibant is a selective 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 dosing regimen for icatibant is determined by the prescribing clinician based on the patient’s condition, weight, and severity of the attack. Healthcare professionals follow the product label and local guidelines to set the appropriate dose.
Is icatibant safe during pregnancy or breastfeeding?+
Safety data for icatibant in pregnancy and lactation are limited. It should only be used when 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 Hikma 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 provides rapid symptom relief, while C1‑esterase products are given intravenously and work by replacing the deficient protein.
What are the storage and handling requirements for icatibant?+
Icatibant should be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. Keep the product in its original packaging until use to maintain stability.
How is icatibant administered?+
Icatibant is supplied as a sterile solution for subcutaneous injection. The prescribed dose is injected into the abdomen or thigh using the pre‑filled syringe provided, following aseptic technique and the instructions of the treating clinician.
What are the most serious risks associated with icatibant?+
Serious risks include severe hypersensitivity reactions such as anaphylaxis, unexpected angioedema unrelated to HAE, and significant hypotension. Patients should be monitored closely after administration, and any signs of a severe 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 receiving ACE inhibitors, neprilysin inhibitors, or other agents that increase bradykinin levels.
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
Intravenous Use
Manufacturer
Hikma Farmacêutica (Portugal), S.A.
Origin
EU

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