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 an injectable solution for subcutaneous use. It is indicated for the treatment of acute attacks of hereditary angioedema in patients with C1‑inhibitor deficiency. The medication is formulated for rapid subcutaneous administration, allowing prompt symptom relief.

GNH India supplies Idanuz as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with a quality‑focused supply chain that ensures product integrity and provides technical documentation for customers.

Manufacturer / TM Owner

Norameda Uab

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Indications & Clinical Uses

Idanuz, a bradykinin B2 receptor antagonist, is used to manage hereditary angioedema attacks.

  • Acute hereditary angioedema (C1‑inhibitor deficiency): rapid reduction of swelling during attacks.
  • Hereditary angioedema type I: alleviates edema and improves patient comfort.
  • Hereditary angioedema type II: provides prompt symptom relief and shortens attack duration.

How It Works

  • Icatibant acts as a competitive antagonist at the bradykinin B2 receptor, binding to the receptor and preventing bradykinin from inducing vasodilation and increased vascular permeability. By blocking this pathway, the drug reduces the edema and pain associated with hereditary angioedema attacks.

Side Effects

Idanuz may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Injection site pain: discomfort at the subcutaneous injection site.
  • Redness or swelling: localized erythema and edema.
  • Nausea: mild gastrointestinal upset.
  • Headache: transient cranial discomfort.

Serious or Rare Side Effects

  • Hypotension: significant drop in blood pressure.
  • Anaphylactic reaction: severe allergic response requiring immediate medical attention.
  • Severe injection site necrosis: tissue damage at the injection area.

Precautions & Warnings

When prescribing Idanuz, consider the following precautions to ensure safe use.

  • Pregnancy: consult a healthcare professional before use.
  • Breastfeeding: evaluate potential risks to the infant.
  • Renal impairment: monitor patients with reduced kidney function.
  • Concomitant ACE inhibitor therapy: use caution due to possible additive bradykinin effects.
  • Known hypersensitivity: avoid administration in patients with previous allergic reactions to icatibant.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Idanuz can interact with other medicines; awareness of these interactions helps manage patient therapy.

Major Interactions (Avoid)

  • ACE inhibitors: may increase bradykinin levels, heightening risk of angioedema.
  • Other bradykinin B2 receptor antagonists: concurrent use can lead to excessive blockade.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may augment risk of swelling or gastrointestinal irritation.
  • Estrogen‑containing contraceptives: can exacerbate hereditary angioedema symptoms.
  • Diuretics: monitor blood pressure and electrolyte balance during therapy.

Frequently Asked Questions

Idanuz contains icatibant and is indicated for the treatment of acute attacks of hereditary angioedema in patients with C1‑inhibitor deficiency. It works by rapidly reducing swelling and improving breathing and comfort during an attack.

Icatibant is a competitive antagonist of the bradykinin B2 receptor. By binding to this receptor, it blocks the action of bradykinin, a peptide that causes vasodilation and increased vascular permeability, thereby preventing the swelling associated with hereditary angioedema attacks.

The dosage of Idanuz is determined by the prescribing healthcare professional based on the patient’s condition, severity of the attack, and clinical guidelines. The prescriber decides the amount and timing of each subcutaneous injection, and patients should follow the exact instructions provided.

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 by a qualified healthcare provider after evaluating the individual situation.

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 handling if needed—and necessary import documentation.

Idanuz (icatibant) is a bradykinin B2 receptor antagonist, whereas alternative therapies such as C1‑inhibitor concentrates replace the deficient protein, and newer agents like lanadelumab are monoclonal antibodies targeting plasma kallikrein. Icatibant offers rapid subcutaneous administration and acts directly on the bradykinin pathway, providing a distinct mechanism of action.

Idanuz should be stored at 2‑8 °C (refrigerated) in its original packaging, protected from light. Do not freeze or shake the product. Before use, allow the solution to reach room temperature if required, and inspect for particulate matter or discoloration; discard if any abnormalities are observed.

Idanuz is given as a subcutaneous injection, typically into the abdomen or thigh. The injection is performed by a healthcare professional or trained patient using the supplied pre‑filled syringe or autoinjector. Proper aseptic technique and correct site rotation help minimize injection‑site reactions.

The most serious risks include severe hypotension, anaphylactic reactions, and rare cases of injection‑site necrosis. Patients should be monitored for signs of systemic allergic response, sudden drop in blood pressure, or worsening swelling, and seek immediate medical attention if any of these occur.

Idanuz is contraindicated in individuals with known hypersensitivity to icatibant or any of the formulation components. It should also be avoided in patients who have experienced severe anaphylactic reactions to the drug and in those for whom alternative approved therapies are more appropriate, as determined by a healthcare professional.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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