Product image of Icatibant Gp-Pharm (Icatibant) supplied by GNH India

Icatibant Gp-Pharm

Active Ingredient:
Icatibant
Origin:
EU

Icatibant Gp-Pharm (Icatibant)

Icatibant, the active ingredient in Icatibant Gp-Pharm, is a bradykinin B2 receptor antagonist presented as a subcutaneous formulation for subcutaneous use. It treats hereditary angioedema (HAE) attacks in patients with this rare genetic disorder.

GNH India supplies Icatibant Gp-Pharm as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Gp-Pharm S.A.

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Indications & Clinical Uses

Icatibant is a bradykinin B2 receptor antagonist used in the management of hereditary angioedema.

  • Hereditary angioedema (HAE) attacks: provides rapid relief of swelling episodes by blocking bradykinin‑mediated vascular permeability.

How It Works

  • Icatibant selectively and competitively binds to the bradykinin B2 receptor, preventing bradykinin from activating the receptor. This inhibition blocks the downstream signaling that leads to vasodilation and increased vascular permeability, thereby reducing the swelling characteristic of hereditary angioedema attacks.

Side Effects

Icatibant may cause a range of adverse reactions, most of which are related to its subcutaneous administration.

Common Side Effects

  • Injection site pain: mild to moderate discomfort at the injection site.
  • Erythema: redness around the injection area.
  • Nausea: occasional feeling of queasiness.
  • Headache: transient head discomfort.
  • Dizziness: brief episodes of light‑headedness.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Hypotension: sudden drop in blood pressure.
  • Angioedema: new swelling episodes unrelated to HAE.
  • Thrombocytopenia: reduced platelet count.
  • Severe infection at injection site: signs of cellulitis or abscess formation.

Precautions & Warnings

Before using Icatibant, consider the following safety measures.

  • Pregnancy: safety not established; use only if potential benefit justifies the risk.
  • Breastfeeding: unknown safety; weigh benefits against possible infant exposure.
  • Renal impairment: monitor patients as clearance may be reduced.
  • Concomitant ACE inhibitors: may increase bradykinin levels; observe for enhanced effects.
  • Estrogen‑containing therapies: may potentiate bradykinin‑mediated reactions; monitor closely.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Icatibant can interact with other medicines that influence bradykinin pathways or cardiovascular function.

Major Interactions (Avoid)

  • ACE inhibitors: increase bradykinin levels and may heighten risk of angioedema.
  • Neprilysin inhibitors: similarly raise bradykinin concentrations.
  • Estrogen‑containing oral contraceptives: may exacerbate bradykinin‑mediated swelling.

Moderate Interactions (Monitor Closely)

  • NSAIDs: can affect renal function and alter drug clearance.
  • Diuretics: may influence blood pressure response.
  • Other antihypertensives: monitor for additive hypotensive effects.
  • Corticosteroids: may mask early signs of infection at injection site.
  • Additional B2 receptor antagonists: assess cumulative pharmacologic impact.

Frequently Asked Questions

Icatibant Gp-Pharm is indicated for the treatment of acute hereditary angioedema (HAE) attacks. It works by rapidly reducing swelling caused by excess bradykinin in patients with this rare genetic condition.

Icatibant is a selective competitive antagonist of the bradykinin B2 receptor. By blocking this receptor, it prevents bradykinin‑induced vasodilation and increased vascular permeability, which are the primary drivers of swelling in HAE.

The dosing regimen for icatibant is determined by the prescribing healthcare professional based on the patient’s clinical condition and regulatory guidelines. Patients should follow the prescriber’s instructions exactly.

Safety data for icatibant in pregnancy and lactation are limited. It should only be used if the potential benefit justifies any possible risk to the fetus or infant, and the decision must be made by a qualified clinician.

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 a deficient protein. Icatibant offers a rapid, subcutaneous option that directly blocks bradykinin, making it useful for patients who prefer self‑administration or who have contraindications to plasma‑derived products.

Icatibant should be stored at 2‑8 °C in a refrigerator, protected from light, and must not be frozen or shaken. Keep the product in its original packaging until use to maintain stability.

Icatibant is given by subcutaneous injection, typically into the abdomen or thigh. The injection is performed by the patient or a caregiver following the prescriber’s instructions and using aseptic technique.

Serious risks include anaphylaxis, severe hypotension, and new episodes of angioedema unrelated to HAE. Patients should be monitored for signs of allergic reaction or sudden blood pressure changes after administration.

Icatibant is contraindicated in individuals with known hypersensitivity to icatibant or any of its excipients. Caution is also advised for patients receiving ACE inhibitors, neprilysin inhibitors, or estrogen‑containing therapies, as these may increase the risk of adverse reactions.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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