GNH USA

Europe — EMA

Icatibant Sandoz

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

Icatibant

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What is Icatibant?

Icatibant, the active ingredient in Icatibant Sandoz, is a bradykinin B2 receptor antagonist presented as an injection for subcutaneous use. It treats acute attacks of hereditary angioedema in adult patients, providing rapid reduction of swelling and pain.

GNH USA supplies Icatibant Sandoz as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable cold‑chain logistics for injectable products. Clients benefit from on‑time delivery, regulatory support, and comprehensive documentation for import and distribution.

What is Icatibant used for?

Icatibant is used to treat hereditary angioedema by blocking the bradykinin pathway. - Hereditary angioedema type I and II: provides rapid relief of swelling during acute attacks in adults. - Hereditary angioedema with normal C1‑INH (type III): reduces symptom severity and duration. - Acquired angioedema related to bradykinin excess: helps control episodic swelling.

What are the side effects of Icatibant?

Icatibant may cause a range of adverse reactions, most of which are related to its injection route or pharmacologic activity.

Common Side Effects: - Injection site pain: mild to moderate discomfort at the injection site. - Redness or swelling at injection site: localized erythema or edema. - Nausea: occasional feeling of queasiness. - Headache: transient head discomfort. - Dizziness: light‑headed sensation.

Serious or Rare Side Effects: - Hypersensitivity reactions: rash, urticaria, or anaphylaxis. - Severe hypotension: marked drop in blood pressure. - Worsening angioedema: paradoxical increase in swelling. - Thrombocytopenia: low platelet count. - Injection‑site infection: signs of local infection requiring medical attention.

What precautions apply to Icatibant?

Before using Icatibant, healthcare professionals should consider several safety measures to minimize risks. - Assess severity of HAE attack: confirm that the episode requires pharmacologic intervention. - Verify patient history of hypersensitivity: avoid use in individuals with known allergy to icatibant or its excipients. - Use with caution in pregnancy or breastfeeding: safety has not been established; weigh potential benefits against risks. - Ensure proper subcutaneous administration technique: train patient or caregiver on correct injection method. - Monitor for signs of severe reactions: observe for anaphylaxis or worsening angioedema after injection. - 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, affecting its safety or efficacy.

Major Interactions (Avoid): - ACE inhibitors: may increase bradykinin levels and exacerbate angioedema. - Other bradykinin B2 receptor antagonists: additive pharmacologic effect may increase risk of adverse events. - Concomitant use of potent vasodilators: can lead to excessive hypotension.

Moderate Interactions (Monitor Closely): - Estrogen‑containing oral contraceptives: may influence frequency of HAE attacks. - C1‑INH concentrate therapy: concurrent use requires clinical monitoring of response. - Non‑steroidal anti‑inflammatory drugs (NSAIDs): may increase risk of injection‑site irritation. - Diuretics: monitor blood pressure due to potential additive hypotensive effect.

Frequently asked questions

What is Icatibant Sandoz used for?+
Icatibant Sandoz is indicated for the treatment of acute attacks of hereditary angioedema (HAE) in adult patients. By rapidly blocking the bradykinin B2 receptor, it helps to reduce swelling and associated discomfort during an HAE episode.
How does icatibant work?+
Icatibant works as a selective antagonist of the bradykinin B2 receptor. It binds competitively to this receptor on vascular endothelial cells, preventing bradykinin from triggering vasodilation and increased vascular permeability, which are the primary mechanisms behind the swelling seen in HAE.
What is the usual dose of icatibant?+
The dose of icatibant is determined by the prescribing healthcare professional based on the patient’s condition and clinical guidelines. The prescriber decides the exact amount, frequency, and duration of therapy for each individual case.
Is icatibant safe in pregnancy or breastfeeding?+
Safety data for icatibant in pregnancy and lactation are limited, and the product is classified as having an unknown pregnancy category. Use during pregnancy or while breastfeeding should only occur if the potential benefit justifies the potential risk to the fetus or infant.
How do I order Icatibant Sandoz from GNH USA?+
To order Icatibant Sandoz, 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 where required) and import documentation.
How does icatibant compare with the main alternative drug or class?+
The primary alternative for HAE is plasma‑derived or recombinant C1‑INH concentrate, which replaces the deficient inhibitor. Icatibant directly blocks the bradykinin B2 receptor, offering a rapid, subcutaneous option that does not require infusion. Choice between them depends on patient preference, attack severity, and clinical response.
What are the storage and handling requirements for Icatibant Sandoz?+
Icatibant Sandoz must be stored refrigerated at 2‑8 °C. Keep the product in its original packaging, protect it from light, and avoid freezing or shaking the vial. If temporary temperature excursions occur, consult the product’s stability data before use.
How is Icatibant administered?+
Icatibant is given as a subcutaneous injection, typically into the abdomen or thigh. The injection can be performed by a healthcare professional or, after proper training, by the patient or a caregiver. The device is a pre‑filled syringe designed for single‑use administration.
What are the most serious risks to watch for when using Icatibant?+
Serious risks include hypersensitivity reactions such as rash, urticaria, or anaphylaxis, severe hypotension, paradoxical worsening of angioedema, thrombocytopenia, and injection‑site infections. Patients should be observed after the first dose and instructed to seek immediate medical attention if any of these events occur.
Who should not use Icatibant?+
Icatibant should be avoided in individuals with known hypersensitivity to icatibant or any of its excipients. Caution is also advised for patients with severe cardiovascular instability or uncontrolled hypotension, as the drug may exacerbate these conditions.
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
Sandoz B.V.
Origin
EU

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