Product image of Icatibant Glenmark (Icatibant) supplied by GNH India

Icatibant Glenmark

Active Ingredient:
Icatibant
Origin:
EU

Icatibant Glenmark (Icatibant)

Icatibant, the active ingredient in Icatibant Glenmark, is a bradykinin B2 receptor antagonist presented as a subcutaneous formulation for injection use. It is indicated for the treatment of acute attacks of hereditary angioedema in patients with C1‑inhibitor deficiency.
GNH India supplies Icatibant Glenmark as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Glenmark Arzneimittel Gmbh

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Indications & Clinical Uses

Icatibant acts on the bradykinin pathway to relieve swelling in hereditary angioedema.

  • Acute hereditary angioedema (C1‑inhibitor deficiency): rapidly reduces edema and restores airway patency during an attack.

How It Works

  • Icatibant selectively blocks the bradykinin B2 receptor, preventing bradykinin from binding and triggering vasodilation and increased vascular permeability. By inhibiting this receptor, the drug curtails the cascade that leads to the swelling characteristic of hereditary angioedema, providing prompt symptom relief.

Side Effects

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: discomfort at the site of subcutaneous administration.
  • Redness or erythema: localized skin reddening.
  • Swelling at injection site: mild to moderate edema.
  • Headache: transient cranial discomfort.
  • Nausea: occasional gastrointestinal upset.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Angioedema of the face or throat: worsening swelling despite therapy.
  • Hypotension: significant drop in blood pressure.
  • Thrombocytopenia: reduced platelet count observed in rare cases.
  • Severe injection site necrosis: tissue death at the injection site.

Precautions & Warnings

Before using Icatibant, consider the following safety measures.

  • Pregnancy: safety has not been established; use only if clearly needed.
  • Breastfeeding: unknown whether the drug is excreted in milk; weigh benefits against risks.
  • Renal impairment: monitor renal function and adjust therapy if necessary.
  • Concomitant ACE inhibitors or neprilysin inhibitors: increased bradykinin levels may heighten risk of angioedema.
  • Storage: Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Icatibant can interact with other agents that affect bradykinin or vascular tone.

Major Interactions (Avoid)

  • ACE inhibitors: may amplify bradykinin‑mediated angioedema.
  • Neprilysin inhibitors: increase bradykinin levels, raising risk of severe swelling.

Moderate Interactions (Monitor Closely)

  • Angiotensin II receptor blockers (ARBs): observe for enhanced hypotensive effects.
  • Estrogen‑containing oral contraceptives: may modestly increase angioedema risk.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): monitor for additive vasodilatory effects.

Frequently Asked Questions

Icatibant Glenmark is used to treat acute attacks of hereditary angioedema caused by C1‑inhibitor deficiency. By blocking the bradykinin B2 receptor, it quickly reduces swelling and helps restore normal airway and tissue function during an episode.

Icatibant works as a selective antagonist of the bradykinin B2 receptor. By preventing bradykinin from binding, it stops the cascade that leads to vasodilation and increased vascular permeability, thereby reducing the swelling that characterises hereditary angioedema attacks.

The dose of icatibant is determined by the prescribing healthcare professional based on the patient’s condition and clinical guidelines. The medication is administered subcutaneously, and the exact regimen should be followed as directed by the prescriber.

Safety of icatibant in pregnancy and lactation has not been fully established. 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.

To order, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain where needed) and import documentation.

Icatibant is a bradykinin B2 receptor antagonist, whereas other therapies such as C1‑inhibitor concentrates replace the deficient protein. Icatibant provides rapid symptom relief through receptor blockade, while C1‑inhibitor products work by restoring the missing inhibitor. Choice depends on clinical response, route preference and patient-specific factors.

Icatibant should be stored at 2‑8 °C in a refrigerator, protected from light. Do not freeze or shake the vial. If temporary storage at room temperature is unavoidable, limit exposure to no more than 30 °C for a short period, and return the product to refrigeration promptly.

Icatibant is given by subcutaneous injection, typically into the abdomen or thigh. The injection is performed by a trained healthcare professional or, after proper instruction, by the patient or caregiver. The site should be rotated for repeated doses to minimize local irritation.

The most serious risks include anaphylaxis, severe angioedema that may worsen despite treatment, and hypotension. Patients should be monitored closely after injection, and any signs of severe allergic reaction or worsening swelling require immediate medical attention.

Icatibant is contraindicated in patients with known hypersensitivity to icatibant or any of its excipients. Caution is also advised for individuals taking ACE inhibitors or neprilysin inhibitors, as the combined effect on bradykinin may increase the risk of angioedema.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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