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

Icatibant Piramal

Active Ingredient:
Icatibant
Origin:
EU

Icatibant Piramal (Icatibant)

Icatibant, the active ingredient in Icatibant Piramal, is a bradykinin B2 receptor antagonist presented as a subcutaneous injection for subcutaneous use. It treats acute attacks of hereditary angioedema caused by C1‑inhibitor deficiency in patients of all ages.

GNH India supplies Icatibant Piramal as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory‑compliant sourcing for global markets.

Manufacturer / TM Owner

Piramal Critical Care B.V.

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Indications & Clinical Uses

Icatibant is used to manage hereditary angioedema by targeting the bradykinin pathway.

  • Hereditary angioedema (C1‑inhibitor deficiency, type I): rapidly reduces swelling and pain during acute attacks.
  • Hereditary angioedema (type II): provides prompt symptom relief and shortens attack duration.
  • Hereditary angioedema (type III or idiopathic): effective in decreasing severity of swelling episodes.

How It Works

  • Icatibant acts as a selective competitive antagonist of the bradykinin B2 receptor. By binding to this receptor, it blocks the actions of bradykinin, preventing bradykinin‑mediated vasodilation and increased vascular permeability that underlie the swelling seen in 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 reddening.
  • Swelling at injection site: transient edema.
  • Headache: mild to moderate intensity.
  • Nausea: occasional upset stomach.
  • Dizziness: brief sensation of light‑headedness.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Angioedema of the face or airway: potentially life‑threatening swelling.
  • Severe hypotension: marked drop in blood pressure.
  • Thrombocytopenia: low platelet count observed in rare cases.
  • Severe injection‑site necrosis: tissue death at the site of injection.

Precautions & Warnings

Before using Icatibant, consider the following safety measures.

  • Contraindication: Do not use in patients with known hypersensitivity to icatibant or any excipients.
  • Pregnancy: Safety has not been established; use only if the potential benefit justifies the risk.
  • Breastfeeding: Caution advised; limited data are available.
  • Monitoring: Observe for signs of anaphylaxis or severe angioedema after injection.
  • Drug interactions: Review concomitant medications for potential bradykinin‑related effects.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Icatibant may interact with other medicines that influence the bradykinin pathway or vascular tone.

Major Interactions (Avoid)

  • Concurrent use of other bradykinin B2 receptor antagonists: may lead to additive pharmacologic effects.
  • Simultaneous administration of C1‑esterase inhibitor concentrates: overlapping therapeutic action can increase risk of adverse events.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors: may reduce the effectiveness of icatibant by increasing bradykinin levels.
  • Angiotensin receptor blockers (ARBs): monitor blood pressure and swelling response.
  • Diuretics: watch for changes in fluid balance that could affect edema management.

Frequently Asked Questions

Icatibant Piramal is indicated for the treatment of acute attacks of hereditary angioedema (HAE) caused by C1‑inhibitor deficiency. It helps to rapidly reduce swelling and associated pain during an HAE episode.

Icatibant works by selectively blocking the bradykinin B2 receptor. This inhibition prevents bradykinin‑induced vasodilation and increased vascular permeability, which are the primary mechanisms driving swelling in hereditary angioedema.

The dose of icatibant is determined by the prescribing healthcare professional based on the patient’s condition and clinical guidelines. The prescriber will decide the exact amount and frequency of administration.

Safety of icatibant in pregnancy and lactation has not been fully established. It should be used only if the potential benefit outweighs any possible risk to the mother or infant, and under medical supervision.

To place an 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 HAE therapies such as C1‑esterase inhibitor concentrates replace the deficient protein. Icatibant offers a rapid, subcutaneous option that directly blocks bradykinin, providing fast symptom relief without the need for intravenous infusion.

Icatibant should be stored at 2‑8 °C (refrigerated). Keep the product in its original packaging, protect it from light, and avoid freezing or shaking the vial to maintain stability.

Icatibant is given by 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.

The most serious risks include severe allergic reactions such as anaphylaxis, airway angioedema, and significant hypotension. Patients should be monitored closely after injection for any signs of these potentially life‑threatening events.

Icatibant should not be used by individuals with a known hypersensitivity to the drug or its excipients. Caution is also advised for patients with uncontrolled cardiovascular disease or those receiving duplicate bradykinin‑targeted therapies.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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