Product image of Idanuz (Icatibant) supplied by GNH India

Idanuz

Active Ingredient:
Icatibant
Origin:
EU

Idanuz (Icatibant)

Icatibant, the active ingredient in Idanuz, is a bradykinin B2 receptor antagonist presented as a solution for injection for subcutaneous use. It treats acute attacks of hereditary angioedema in patients with a confirmed diagnosis.
GNH India supplies Idanuz as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Norameda Uab

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Indications & Clinical Uses

Idanuz is a bradykinin B2 receptor antagonist indicated for the treatment of hereditary angioedema attacks.

  • Acute hereditary angioedema: provides rapid relief of swelling episodes and reduces disease burden during attacks.

How It Works

  • Icatibant selectively and competitively blocks the bradykinin B2 receptor on vascular endothelial cells. By preventing bradykinin binding, it inhibits the downstream signaling that causes vasodilation and increased vascular permeability, thereby reducing the swelling and pain associated with hereditary angioedema attacks.

Side Effects

Common adverse reactions are usually mild and related to the injection site or transient systemic responses.

Common Side Effects

  • Injection site pain: discomfort at the subcutaneous injection site.
  • Redness or erythema: localized skin reddening.
  • Swelling at injection site: mild, temporary edema.
  • Nausea: occasional feeling of queasiness.
  • Headache: mild to moderate intensity.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Angioedema of the face or throat: may compromise airway.
  • Hypotension: sudden drop in blood pressure.
  • Severe injection site necrosis: tissue damage at the site.
  • Thrombocytopenia: low platelet count observed in rare cases.

Precautions & Warnings

Before using Idanuz, consider the following safety measures.

  • Pregnancy: safety not established; use only if potential benefit justifies the risk.
  • Breastfeeding: unknown excretion; weigh benefits against possible infant exposure.
  • Renal impairment: no dosage adjustment required, but monitor for accumulation.
  • Concomitant ACE inhibitors: may increase risk of angioedema; assess necessity.
  • Hypersensitivity: discontinue immediately if signs of allergic reaction appear.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Icatibant may interact with other agents that influence bradykinin pathways or immune responses.

Major Interactions (Avoid)

  • ACE inhibitors: can raise bradykinin levels and heighten angioedema risk.
  • Neprilysin inhibitors (e.g., sacubitril): may increase bradykinin concentrations, potentially reducing icatibant efficacy.

Moderate Interactions (Monitor Closely)

  • Antihistamines: may mask early signs of an allergic reaction.
  • Systemic corticosteroids: could alter assessment of swelling severity.
  • Other subcutaneous injections at the same site: may increase local irritation or infection risk.

Frequently Asked Questions

Idanuz is a branded formulation of icatibant, indicated for the treatment of acute attacks of hereditary angioedema. It works by rapidly reducing swelling and associated symptoms during an episode, providing relief for patients with this rare, hereditary 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 mechanisms that cause the swelling seen in hereditary angioedema attacks.

The dose of Idanuz is determined by the prescribing healthcare professional based on the patient’s clinical condition and regulatory guidelines. The prescriber will decide the exact amount and frequency required for each acute attack.

Safety data for icatibant in pregnancy and lactation are limited. It should only be used if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision should be made in consultation with a qualified healthcare provider.

To request Idanuz, 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 where required) and necessary import documentation.

Idanuz (icatibant) is a bradykinin B2 receptor antagonist, whereas other options such as C1‑esterase inhibitor concentrates replace a deficient protein, and newer monoclonal antibodies target different pathways. Icatibant offers a subcutaneous, rapid‑acting option that directly blocks bradykinin‑mediated swelling.

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

Idanuz is supplied as a solution for injection and is administered subcutaneously, typically into the abdomen or thigh. The injection is performed by a trained healthcare professional or, after proper instruction, by the patient or caregiver.

The most serious risks include severe allergic reactions such as anaphylaxis, angioedema involving the face or throat that could compromise the airway, and rare cases of hypotension. Patients should be monitored closely after administration for any signs of these reactions.

Idanuz is contraindicated in individuals with known hypersensitivity to icatibant or any of the formulation components. Caution is also advised for patients with a history of severe allergic reactions, uncontrolled hypertension, or those receiving ACE inhibitors without appropriate medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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