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

Icatibant Hikma

Active Ingredient:
Icatibant
Origin:
EU

Icatibant Hikma (Icatibant)

Icatibant, the active ingredient in Icatibant Hikma, is a bradykinin B2 receptor antagonist presented as a sterile solution for injection for intravenous administration. It is indicated for the treatment of acute attacks of hereditary angioedema type I and II in patients with a confirmed diagnosis, helping to reduce swelling and associated symptoms.

GNH India supplies Icatibant Hikma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable global distribution.

Manufacturer / TM Owner

Hikma Farmacêutica (Portugal), S.A.

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Indications & Clinical Uses

Icatibant acts on the bradykinin pathway to control swelling in hereditary angioedema.

  • Hereditary angioedema type I: reduces swelling during acute attacks.
  • Hereditary angioedema type II: alleviates symptoms of acute episodes.
  • Acute hereditary angioedema attacks: provides rapid symptom control.

How It Works

  • Icatibant selectively blocks the bradykinin B2 receptor, preventing bradykinin from binding and triggering vasodilation and increased vascular permeability. By inhibiting this receptor, the drug curtails the cascade that leads to the rapid formation of edema in hereditary angioedema, thereby limiting swelling and associated discomfort.

Side Effects

Common Side Effects

  • Injection site pain: mild to moderate discomfort at the injection site.
  • Erythema: localized redness around the injection area.
  • Nausea: occasional feeling of queasiness.
  • Headache: transient mild to moderate headache.
  • Dizziness: brief episodes of light‑headedness.
  • Flushing: temporary warmth and reddening of the skin.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Angioedema: swelling of face, lips, or throat despite treatment.
  • Hypotension: sudden drop in blood pressure.
  • Severe allergic reaction: rash, bronchospasm, or swelling.
  • Thrombocytopenia: low platelet count observed in rare cases.

Precautions & Warnings

Before initiating therapy, clinicians should consider patient‑specific factors and monitor for adverse events.

  • Assess patient history: verify diagnosis of HAE type I or II before use.
  • Monitor for hypersensitivity: observe for signs of allergic reaction after injection.
  • Avoid use in patients with known hypersensitivity to icatibant or formulation components.
  • Use with caution in pregnant or breastfeeding women: limited data, weigh benefits and risks.
  • Renal or hepatic impairment: no dosage adjustment known, monitor clinical response.
  • 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: may increase bradykinin levels, raising risk of angioedema.
  • Angiotensin receptor blockers: similar risk of enhanced bradykinin activity.
  • Other bradykinin B2 antagonists: additive pharmacologic effect, avoid concurrent use.

Moderate Interactions (Monitor Closely)

  • Corticosteroids: may mask signs of infection, monitor patient closely.
  • Antihistamines: could alter assessment of allergic reactions, observe for changes.
  • NSAIDs: may exacerbate gastrointestinal irritation, watch for adverse GI events.

Frequently Asked Questions

Icatibant Hikma is used to treat acute attacks of hereditary angioedema (HAE) types I and II. It works by rapidly reducing swelling and associated symptoms during an HAE episode, providing relief for patients with a confirmed diagnosis.

Icatibant 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 drivers of swelling in hereditary angioedema.

The dosage and administration schedule for Icatibant Hikma are determined by the prescribing healthcare professional based on the patient’s condition, severity of the attack, and clinical guidelines. The prescriber will set the appropriate dose.

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.

To order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain where required) and import documentation.

Icatibant is a bradykinin B2 receptor antagonist, whereas other HAE therapies such as C1‑esterase inhibitor concentrates replace deficient proteins. Icatibant offers a rapid, subcutaneous route of administration and directly blocks bradykinin, providing an alternative mechanism of action.

Icatibant Hikma should be stored at 2‑8 °C in a refrigerator, protected from light. Do not freeze the solution and avoid shaking the vial. Keep it in the original packaging until ready for use.

The product is supplied as a sterile solution for injection and is administered intravenously by a qualified healthcare professional. The injection is given into a vein, typically in a clinical setting, following the prescriber’s instructions.

The most serious risks include anaphylaxis, severe angioedema, and hypotension. Patients should be monitored closely after administration for any signs of allergic reaction or sudden drop in blood pressure, and emergency measures should be available.

Icatibant should not be used in individuals with known hypersensitivity to icatibant or any component of the formulation. It is also contraindicated in patients receiving other bradykinin B2 antagonists or those with uncontrolled severe allergic conditions.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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