GNH USA

Europe — EMA

Icatibant Teva

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

Icatibant Acetate

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What is Icatibant Acetate?

Icatibant acetate, the active ingredient in Icatibant Teva, is a bradykinin B2 receptor antagonist presented as a 30 mg/1 mL injection solution for subcutaneous administration. It is indicated for the treatment of acute attacks of hereditary angioedema in patients with C1‑inhibitor deficiency, providing rapid symptom relief by blocking bradykinin‑mediated vascular effects.

GNH USA supplies Icatibant Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with capabilities for cold‑chain logistics and regulatory support, and ensuring product integrity throughout transport and storage.

What is Icatibant Acetate used for?

Icatibant Teva is a bradykinin B2 receptor antagonist used in the management of hereditary angioedema. - Acute HAE attacks (C1‑inhibitor deficiency): rapid reduction of swelling and pain. - Hereditary angioedema type I attacks: alleviation of edema during episodes. - Hereditary angioedema type II attacks: alleviation of edema during episodes.

What are the side effects of Icatibant Acetate?

Icatibant Teva may be associated with injection‑site reactions and systemic adverse events.

Common Side Effects: - Injection site pain: mild to moderate discomfort at the injection area. - Redness: localized erythema around the injection site. - Swelling: transient edema at the site. - Headache: mild headache occurring after administration.

Serious or Rare Side Effects: - Hypersensitivity reaction: rash, urticaria, or anaphylaxis requiring immediate medical attention. - Severe abdominal pain: persistent pain that may indicate an adverse gastrointestinal response. - Thrombocytopenia: low platelet count observed in rare cases, monitored by laboratory tests.

What precautions apply to Icatibant Acetate?

When using Icatibant Teva, clinicians should consider several precautionary measures to ensure safe administration. - Pregnancy: safety has not been established; use only if potential benefit justifies risk. - Breastfeeding: unknown safety; weigh benefits against potential infant exposure. - Renal impairment: no dosage adjustment required, but monitor for accumulation. - Concomitant ACE inhibitors: may increase risk of angioedema; observe closely. - Allergy to formulation components: avoid use in patients with known hypersensitivity. - Store at 2-8 °C: keep refrigerated, protect from light, do not freeze or shake.

What does Icatibant Acetate interact with?

Icatibant Teva has a limited interaction profile, but certain drug combinations require attention.

Major Interactions (Avoid): - ACE inhibitors: additive risk of angioedema; avoid concurrent use. - Estrogen‑containing contraceptives: may exacerbate hereditary angioedema; monitor closely.

Moderate Interactions (Monitor Closely): - C1‑inhibitor concentrate: may reduce need for icatibant; monitor clinical response. - Antifibrinolytics (e.g., tranexamic acid): possible additive effect on coagulation; observe. - Other bradykinin pathway modulators: may alter efficacy; assess therapeutic outcome.

Frequently asked questions

What is Icatibant Teva used for?+
Icatibant Teva is indicated for the treatment of acute attacks of hereditary angioedema in patients who have a deficiency of C1‑inhibitor. By rapidly blocking the effects of bradykinin, it helps to reduce swelling, pain, and other symptoms associated with an HAE episode.
How does icatibant acetate work?+
Icatibant acetate works by selectively and competitively antagonizing the bradykinin B2 receptor on vascular endothelial cells. This blocks bradykinin‑mediated signaling that leads to vasodilation and increased vascular permeability, thereby preventing the swelling characteristic of hereditary angioedema.
What is the usual dose of Icatibant Teva?+
The dose of Icatibant Teva is determined by the prescribing clinician based on the patient’s condition and clinical response. Typically, a single subcutaneous injection of 30 mg is administered at the onset of an HAE attack, but the exact regimen should follow the prescriber’s instructions.
Is Icatibant Teva safe during pregnancy or breastfeeding?+
Safety data for Icatibant Teva in pregnancy and lactation are limited. It should only be used if the potential benefit 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 Teva from GNH USA?+
To order Icatibant Teva, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, cold‑chain shipping details and any necessary import documentation.
How does Icatibant compare with the main alternative therapy?+
The primary alternative for acute HAE attacks is C1‑inhibitor concentrate, which replaces the deficient protein. Icatibant directly blocks bradykinin receptors, offering a rapid, subcutaneous option that does not require plasma‑derived products. Choice of therapy depends on patient preference, availability, and specific clinical considerations.
What are the storage and handling requirements for Icatibant Teva?+
Icatibant Teva must be stored refrigerated between 2 °C and 8 °C. It should be kept in its original packaging, protected from light, and must not be frozen or shaken. If temporary temperature excursions occur, the product should be inspected for any changes before use.
How is Icatibant Teva administered?+
Icatibant Teva is administered as a single subcutaneous injection, typically into the abdomen or thigh. The injection is performed by a trained healthcare professional or, in some cases, by the patient after appropriate instruction. No infusion set or IV access is required.
What are the most serious risks to watch for with Icatibant Teva?+
Serious risks include hypersensitivity reactions such as rash, urticaria, or anaphylaxis, and rare cases of severe abdominal pain or thrombocytopenia. Patients should be monitored for any signs of allergic response or unexpected systemic symptoms after injection and seek immediate medical attention if they occur.
Who should not use Icatibant Teva?+
Icatibant Teva should be avoided in individuals with known hypersensitivity to icatibant acetate or any of the formulation excipients. Caution is also advised for patients with a history of severe allergic reactions, and it is not recommended for use in pregnancy or breastfeeding unless clearly justified by a physician.
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 Acetate
Route
Subcutaneous Use
Manufacturer
Teva B.V
Origin
EU

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