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

Icatibant Accord

Active Ingredient:
Icatibant
Origin:
EU

Icatibant Accord (Icatibant)

Icatibant, the active ingredient in Icatibant Accord, is a bradykinin B2 receptor antagonist presented as an injectable solution for subcutaneous use. It is indicated for the treatment of acute attacks of hereditary angioedema in adult patients. The product is authorized in the European Union and is administered by a healthcare professional.

GNH India supplies Icatibant Accord as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, providing reliable cold‑chain logistics and regulatory support for global distribution, and ensuring product integrity.

Manufacturer / TM Owner

Accord Healthcare S.L.U.

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Indications & Clinical Uses

  • Icatibant is used to treat conditions mediated by excessive bradykinin activity, primarily hereditary angioedema.
  • Acute hereditary angioedema attacks (type I): rapid reduction of subcutaneous and submucosal edema.
  • Acute hereditary angioedema attacks (type II): alleviation of swelling and associated discomfort.
  • Hereditary angioedema in adults (any type): control of bradykinin‑mediated vascular permeability.

How It Works

  • Icatibant acts as a selective competitive antagonist at the bradykinin B2 receptor. By binding to this receptor, it blocks the actions of endogenous bradykinin, preventing bradykinin‑induced vasodilation and increased vascular permeability that underlie the swelling seen in hereditary angioedema.

Side Effects

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

Common Side Effects

  • Injection site pain or erythema.
  • Local swelling or induration at the injection site.
  • Nausea or mild headache.
  • Dizziness or fatigue.

Serious or Rare Side Effects

  • Severe hypersensitivity reactions, including anaphylaxis.
  • Acute hypotension.
  • Paradoxical angioedema or airway compromise.
  • Thrombocytopenia or other hematologic abnormalities.

Precautions & Warnings

  • When using Icatibant, certain precautions should be observed.
  • Pregnancy: safety not established; use only if benefit outweighs risk.
  • Breastfeeding: unknown safety; consider potential risks.
  • Renal impairment: monitor as drug is primarily renally excreted.
  • Concomitant ACE inhibitors: may increase bradykinin levels; observe for enhanced edema.
  • Hypersensitivity: discontinue immediately if 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 medicines that affect bradykinin pathways.

Major Interactions (Avoid)

  • ACE inhibitors: additive bradykinin effect may worsen angioedema.
  • Angiotensin receptor blockers: similar risk of increased bradykinin activity.
  • Estrogen‑containing contraceptives: may raise frequency of HAE attacks.

Moderate Interactions (Monitor Closely)

  • NSAIDs: can exacerbate swelling in susceptible individuals.
  • Diuretics: may alter fluid balance and affect symptom severity.
  • Other B2 receptor antagonists: no additive benefit and may increase adverse event risk.

Frequently Asked Questions

Icatibant Accord is indicated for the treatment of acute attacks of hereditary angioedema (HAE) in adult patients. It works by rapidly reducing swelling caused by excess bradykinin, providing symptom relief during HAE episodes.

Icatibant is a selective competitive antagonist of the bradykinin B2 receptor. By blocking this receptor, it prevents bradykinin‑mediated vasodilation and increased vascular permeability, which are the primary mechanisms driving the swelling seen in hereditary angioedema.

The dose and administration schedule are determined by the prescribing clinician based on the patient’s condition and response. Icatibant is administered as a subcutaneous injection, and the exact amount is individualized for each acute HAE episode.

Safety data for Icatibant in pregnancy and lactation are limited. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the decision should be made in consultation with a healthcare professional.

To 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) and necessary import documentation.

The main alternative class for HAE is plasma‑derived or recombinant C1‑esterase inhibitors, which replace the deficient protein. Icatibant, by contrast, blocks the bradykinin B2 receptor directly, offering a rapid, receptor‑targeted approach without the need for plasma products.

Icatibant Accord must be stored at 2‑8 °C (refrigerated). Keep the vial in its original packaging, protect it from light, and avoid freezing or shaking the solution. Do not use the product if it has been exposed to temperatures outside this range.

The medication is given by subcutaneous injection, usually into the abdomen or thigh. Administration should be performed by a qualified healthcare professional or a trained patient, following aseptic technique and rotating injection sites to minimize local reactions.

Serious risks include severe hypersensitivity reactions such as anaphylaxis, acute hypotension, and paradoxical angioedema that can affect the airway. Patients should be monitored closely after injection, and any signs of severe allergic response require immediate medical attention.

Icatibant is contraindicated in individuals with known hypersensitivity to icatibant or any of its excipients. Caution is also advised for patients with severe renal impairment or those receiving medications that significantly increase bradykinin levels, as the risk of adverse reactions may be higher.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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