Product image of Icatibant Ratiopharm (Icatibant Acetate) supplied by GNH India

Icatibant Ratiopharm

Active Ingredient:
Icatibant Acetate
Origin:
EU

Icatibant Ratiopharm (Icatibant Acetate)

Icatibant acetate, the active ingredient in Icatibant Ratiopharm, is a bradykinin B2 receptor antagonist presented as a subcutaneous injection for subcutaneous use. It treats hereditary angioedema (HAE) attacks in patients with a confirmed diagnosis.

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

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

  • Icatibant Ratiopharm is used to treat conditions mediated by excessive bradykinin activity, primarily hereditary angioedema.
  • Hereditary angioedema (HAE) attacks: rapid reduction of swelling and pain during acute episodes.

How It Works

  • Icatibant acetate selectively blocks the bradykinin B2 receptor on vascular endothelial cells, preventing bradykinin‑induced vasodilation and increased vascular permeability. By inhibiting this pathway, the drug reduces the fluid extravasation that causes the swelling characteristic of hereditary angioedema attacks.

Side Effects

Common Side Effects

  • Injection site pain or erythema
  • Local swelling or induration
  • Nausea or mild headache
  • Dizziness or fatigue

Serious or Rare Side Effects

  • Hypersensitivity reactions including rash or urticaria
  • Anaphylaxis or severe allergic response
  • Marked hypotension
  • Angioedema unrelated to HAE
  • Thrombocytopenia or abnormal bleeding
  • Severe infection at the injection site

Precautions & Warnings

Before initiating therapy, confirm the diagnosis of hereditary angioedema and assess for prior hypersensitivity to bradykinin antagonists.

  • Allergy assessment: avoid in patients with known B2‑receptor antagonist allergy.
  • Monitoring: observe for signs of severe hypotension or anaphylaxis after injection.
  • Concomitant therapy: use under medical supervision when combined with ACE inhibitors or other bradykinin‑modulating agents.
  • Pregnancy and lactation: discuss potential risks with a healthcare professional before use.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Icatibant may interact with drugs that influence bradykinin levels or vascular tone.

Major Interactions (Avoid)

  • ACE inhibitors: can increase bradykinin and heighten risk of angioedema.
  • Neprilysin inhibitors: may elevate bradykinin concentrations.
  • Other bradykinin B2 antagonists: additive pharmacologic effect.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may exacerbate swelling or pain.
  • Oral contraceptives: potential for altered vascular response.
  • Diuretics: monitor blood pressure changes.
  • Antihistamines: may mask early signs of hypersensitivity.

Frequently Asked Questions

Icatibant Ratiopharm is prescribed for the acute treatment of hereditary angioedema (HAE) attacks. It works by rapidly reducing the swelling and pain that occur during an HAE episode, providing relief for patients with a confirmed diagnosis.

Icatibant acetate is a selective antagonist of the bradykinin B2 receptor. By blocking this receptor, it prevents bradykinin‑mediated vasodilation and increased vascular permeability, which are the primary mechanisms that cause the swelling seen in HAE attacks.

The dosage and administration schedule for Icatibant Ratiopharm are determined by the prescribing healthcare professional based on the patient’s clinical condition and regulatory guidelines. Patients should follow the prescriber’s instructions precisely.

Safety data for icatibant acetate in pregnancy and lactation are limited. Women who are pregnant, planning to become pregnant, or breastfeeding should discuss potential risks and benefits with their physician before using the product.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying 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 handling if needed) and import documentation.

Icatibant is a bradykinin B2 receptor antagonist, whereas other approved HAE therapies include C1‑esterase inhibitor concentrates and kallikrein inhibitors. Icatibant’s subcutaneous route offers rapid onset of action and does not require plasma‑derived products, making it a distinct option for patients who prefer a synthetic agent.

Icatibant Ratiopharm 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.

The medication is given by subcutaneous injection, typically into the abdomen or thigh. A healthcare professional or trained patient can perform the injection using the supplied pre‑filled syringe, following aseptic technique and the prescriber’s dosing instructions.

Serious risks include hypersensitivity reactions such as anaphylaxis, severe hypotension, and rare cases of angioedema unrelated to HAE. Patients should be monitored closely after the first dose and instructed to seek immediate medical attention if they experience signs of a severe allergic reaction.

Icatibant is contraindicated in individuals with a known allergy to icatibant acetate or any component of the formulation. It should also be avoided in patients who have experienced severe hypersensitivity to other bradykinin B2 receptor antagonists.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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