Product image of Icatibant Genus Pharmaceuticals (Icatibant) supplied by GNH India

Icatibant Genus Pharmaceuticals

Active Ingredient:
Icatibant
Origin:
EU

Icatibant Genus Pharmaceuticals (Icatibant)

Icatibant, the active ingredient in Icatibant Genus Pharmaceuticals, is a bradykinin B2 receptor antagonist presented as a 30 mg/1 mL injection solution for subcutaneous use. It treats acute attacks of hereditary angioedema in patients with C1‑inhibitor deficiency and provides rapid relief of swelling episodes associated with the disease.

GNH India supplies Icatibant Genus Pharmaceuticals as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics, including emergency departments and specialized treatment centres, worldwide.

Manufacturer / TM Owner

Genus Pharmaceuticals Limited

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Indications & Clinical Uses

Icatibant is used to treat conditions mediated by excessive bradykinin activity, primarily hereditary angioedema.

  • Hereditary angioedema (HAE) with C1‑inhibitor deficiency: provides rapid reduction of swelling during acute attacks.
  • Hereditary angioedema type I: alleviates edema during episodes.
  • Hereditary angioedema type II: blocks bradykinin‑mediated vascular leakage in attacks.

How It Works

  • Icatibant acts as a selective competitive antagonist of the bradykinin B2 receptor. By binding to this receptor, it prevents bradykinin from inducing vasodilation and increasing vascular permeability, thereby reducing the fluid extravasation that causes the swelling characteristic of hereditary angioedema attacks.

Side Effects

Icatibant may cause a range of adverse reactions following subcutaneous administration.

Common Side Effects

  • Injection site pain: mild to moderate discomfort at the injection site.
  • Redness or erythema: localized skin redness.
  • Swelling at injection site: transient edema.
  • Nausea: occasional gastrointestinal upset.
  • Headache: mild to moderate intensity.
  • Dizziness: transient light‑headedness.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Angioedema unrelated to HAE: unexpected swelling in other body parts.
  • Severe hypotension: marked drop in blood pressure.
  • Urticaria: widespread hives.
  • Infection at injection site: signs of local infection.
  • Thrombocytopenia: low platelet count observed in rare cases.

Precautions & Warnings

Before using Icatibant, consider the following safety measures.

  • Pregnancy: safety unknown; avoid unless the potential benefit justifies the risk.
  • Breastfeeding: unknown safety; weigh benefits against possible risks.
  • Renal impairment: use with caution; monitor renal function.
  • Concomitant ACE inhibitors: may increase bradykinin levels; observe for angioedema.
  • Hypersensitivity: discontinue if a severe allergic reaction occurs.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Icatibant can interact with other medications that affect bradykinin pathways or fluid balance.

Major Interactions (Avoid)

  • ACE inhibitors: additive bradykinin effects may raise angioedema risk.
  • Other bradykinin B2 antagonists: duplication of pharmacologic effect.
  • Combined use with ARBs and ACE inhibitors: heightened bradykinin activity.

Moderate Interactions (Monitor Closely)

  • Diuretics: may influence fluid status and blood pressure.
  • NSAIDs: could increase local injection‑site irritation.
  • Antihistamines: may mask early signs of hypersensitivity reactions.

Frequently Asked Questions

Icatibant is indicated for the treatment of acute attacks of hereditary angioedema (HAE) in patients who have a deficiency of C1‑inhibitor. It works to quickly reduce swelling and alleviate symptoms during an HAE episode.

Icatibant selectively blocks the bradykinin B2 receptor, preventing bradykinin from causing vasodilation and increased vascular permeability. This inhibition stops the fluid leakage that leads to the swelling seen in hereditary angioedema attacks.

The prescribed dose of Icatibant is determined by the treating physician based on the patient’s clinical condition and regulatory guidelines. The medication is supplied as a 30 mg/1 mL injection solution for subcutaneous administration.

The safety of Icatibant in pregnancy and while breastfeeding has not been established. Use is only recommended if the potential benefit justifies any possible risk to the mother or infant, and it should be decided by a qualified healthcare professional.

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

Icatibant is a bradykinin B2 receptor antagonist, whereas other approved HAE therapies include C1‑inhibitor concentrates and kallikrein inhibitors. Icatibant offers a subcutaneous route and rapid onset of action, making it suitable for self‑administration during acute attacks, while C1‑inhibitor products are typically given intravenously.

Icatibant should be stored at 2‑8 °C (refrigerated). Keep the product in its original packaging, protect it from light, and do not freeze or shake the vial. If temporary storage at room temperature is unavoidable, limit exposure to no more than 30 minutes.

Icatibant is administered as a single subcutaneous injection into the abdomen, thigh, or upper arm. The injection is performed by a trained healthcare professional or, in some cases, by the patient after appropriate instruction. The site should be rotated for each dose to minimize local reactions.

The most serious risks include anaphylaxis, severe hypotension, and paradoxical angioedema unrelated to hereditary angioedema. Patients should be monitored for signs of allergic reaction, sudden blood pressure drops, or unexpected swelling, and seek immediate medical attention if these occur.

Icatibant is contraindicated in individuals with known hypersensitivity to the active ingredient or any excipients in the formulation. It should also be avoided in patients who are simultaneously receiving other bradykinin B2 antagonists or who have uncontrolled severe cardiovascular disease without medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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