GNH USA

Europe — EMA

Icatibant Glenmark

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

Icatibant

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What is Icatibant?

Icatibant, the active ingredient in Icatibant Glenmark, is a bradykinin B2 receptor antagonist presented as a sterile solution for injection for subcutaneous administration. It is indicated for the treatment of acute attacks of hereditary angioedema type I and type II, providing rapid symptom relief in affected individuals.

GNH USA supplies Icatibant Glenmark as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring quality‑controlled sourcing and reliable cold‑chain logistics where required. The company adheres to stringent regulatory standards and provides comprehensive documentation for import and distribution.

What is Icatibant used for?

Icatibant is used to treat hereditary angioedema, a disorder characterized by excessive bradykinin‑mediated swelling.

- Hereditary angioedema type I: reduces swelling and pain during acute attacks. - Hereditary angioedema type II: provides rapid relief of edema in acute episodes. - Hereditary angioedema (all types): controls symptoms of sudden swelling episodes.

What are the side effects of Icatibant?

Icatibant may cause a range of adverse reactions, varying from mild to serious.

Common Side Effects: - Injection site pain: discomfort at the subcutaneous injection site. - Redness or swelling at injection site: localized inflammatory response. - Nausea: mild gastrointestinal upset. - Headache: transient cranial discomfort.

Serious or Rare Side Effects: - Anaphylaxis: severe allergic reaction requiring immediate medical attention. - Airway angioedema: swelling that may compromise breathing. - Severe hypotension: marked drop in blood pressure. - Thrombocytopenia: low platelet count that can increase bleeding risk.

What precautions apply to Icatibant?

Before using Icatibant, certain safety considerations should be observed.

- Confirm diagnosis: ensure the patient has hereditary angioedema type I or II. - Monitor hypersensitivity: watch for signs of allergic reaction during and after injection. - Use under medical supervision: administration should be directed by a qualified healthcare professional. - Avoid in known hypersensitivity: do not give to patients with documented allergy to icatibant or its excipients. - Pregnancy and lactation: safety is unknown; weigh potential benefits against risks. - 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 affect the bradykinin pathway or hemodynamic stability.

Major Interactions (Avoid): - ACE inhibitors: may increase bradykinin levels and worsen angioedema. - Concomitant use of other bradykinin B2 antagonists: can lead to unpredictable pharmacodynamic effects.

Moderate Interactions (Monitor Closely): - C1‑esterase inhibitor concentrates: may alter clinical response when used together. - Other prophylactic HAE agents (e.g., androgens): monitor for additive effects on swelling control. - Antihistamines: may mask early signs of an allergic reaction, requiring careful observation.

Frequently asked questions

What is Icatibant Glenmark used for?+
Icatibant Glenmark is indicated for the treatment of acute attacks of hereditary angioedema type I and type II. It works by rapidly reducing swelling and associated pain during an episode, providing symptom relief for patients with confirmed HAE.
How does icatibant work in the body?+
Icatibant is a selective antagonist of the bradykinin B2 receptor. By binding to this receptor, it blocks the action of bradykinin, a peptide that causes blood vessels to dilate and become more permeable, thereby preventing the fluid leakage that leads to swelling in hereditary angioedema.
What is the usual dose of Icatibant Glenmark?+
The dose of Icatibant Glenmark is determined by the prescribing healthcare professional based on the patient’s condition, severity of the attack, and clinical guidelines. Dosage instructions are provided on the prescription label and should be followed exactly as directed.
Is Icatibant safe to use during pregnancy or breastfeeding?+
The safety of Icatibant during pregnancy and lactation has not been established. Healthcare providers will weigh the potential benefits against any possible risks before prescribing it to pregnant or nursing individuals.
How do I order Icatibant Glenmark from GNH USA?+
To 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 handling if needed), and import documentation.
How does Icatibant compare with other HAE treatments?+
Icatibant is a bradykinin B2 receptor antagonist, whereas other approved therapies such as C1‑esterase inhibitors replace a deficient protein, and newer monoclonal antibodies target different pathways. Icatibant offers a subcutaneous, rapid‑acting option that directly blocks bradykinin, making it useful for patients who prefer self‑administration during attacks.
What are the storage requirements for Icatibant Glenmark?+
The product should be stored refrigerated at 2 °C to 8 °C. Keep the vial in its original packaging, protect it from light, and avoid freezing or shaking the solution. If temporary storage at room temperature is unavoidable, limit exposure to no more than 30 °C for a short period.
How is Icatibant Glenmark administered?+
Icatibant Glenmark is supplied as a sterile solution for subcutaneous injection. The patient or a trained caregiver injects the dose into the subcutaneous tissue, typically in the abdomen or thigh, using the pre‑filled syringe provided. Injection technique and site rotation are explained by the prescribing clinician.
What are the most serious risks associated with Icatibant?+
Serious risks include anaphylaxis, airway angioedema that can compromise breathing, severe hypotension, and rare hematologic abnormalities such as thrombocytopenia. Patients should be monitored after injection, and any signs of severe allergic reaction or breathing difficulty require immediate medical attention.
Who should not use Icatibant Glenmark?+
Icatibant Glenmark should not be used by individuals with known hypersensitivity to icatibant or any of its excipients. It is also contraindicated in patients who have experienced severe allergic reactions to related bradykinin B2 antagonists. Clinical judgment is required for patients with unstable cardiovascular 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
Glenmark Arzneimittel Gmbh
Origin
EU

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