Product image of Icatibant Glenmark Pharmaceuticals Europe (Icatibant Acetate) supplied by GNH India

Icatibant Glenmark Pharmaceuticals Europe

Active Ingredient:
Icatibant Acetate
Origin:
EU

Icatibant Glenmark Pharmaceuticals Europe (Icatibant Acetate)

Icatibant acetate, the active ingredient in Icatibant Glenmark Pharmaceuticals Europe, is a bradykinin B2 receptor antagonist presented as a sterile solution for subcutaneous injection. It is indicated for the treatment of acute hereditary angioedema attacks in patients with C1‑inhibitor deficiency, providing rapid symptom relief by blocking bradykinin‑mediated vascular effects.

GNH India supplies Icatibant Glenmark Pharmaceuticals Europe as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company ensures quality compliance and reliable cold‑chain logistics for this injectable therapy.

Manufacturer / TM Owner

Glenmark Pharmaceuticals Europe Limited

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Indications & Clinical Uses

Icatibant is a bradykinin B2 receptor antagonist used in the management of hereditary angioedema.

  • Hereditary angioedema type I: reduces swelling and pain during acute attacks.
  • Hereditary angioedema type II: blocks bradykinin‑mediated edema to control episodes.
  • Hereditary angioedema attacks (C1‑inhibitor deficiency): provides rapid relief of symptoms.

How It Works

  • Icatibant acetate acts as a competitive antagonist at the bradykinin B2 receptor. By binding to this receptor, it prevents bradykinin from inducing vasodilation and increasing vascular permeability, thereby limiting the fluid extravasation and swelling that characterize hereditary angioedema attacks.

Side Effects

Icatibant is generally well tolerated, but adverse reactions can occur.

Common Side Effects

  • Injection site pain: discomfort at the injection site.
  • Redness or erythema: mild skin irritation.
  • Swelling at injection site: localized edema.
  • Nausea: occasional gastrointestinal upset.
  • Headache: mild to moderate.
  • Dizziness: transient light‑headedness.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical care.
  • Angioedema: unexpected swelling of face, lips, or throat.
  • Hypotension: significant drop in blood pressure.
  • Severe injection‑site reactions: necrosis or ulceration.
  • Urticaria: widespread hives.
  • Thrombocytopenia: low platelet count observed rarely.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient history and monitor for potential adverse events.

  • Assess patient history: confirm hereditary angioedema diagnosis prior to use.
  • Monitor for hypersensitivity: watch for signs of allergic reaction during and after injection.
  • Avoid in known hypersensitivity: do not use if the patient is allergic to icatibant or excipients.
  • Use with caution in pregnancy or breastfeeding: safety not established, weigh benefits against risks.
  • Renal or hepatic impairment: no dosage adjustment required but 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 medications that influence bradykinin pathways or cardiovascular function.

Major Interactions (Avoid)

  • ACE inhibitors: may increase bradykinin levels, potentially reducing icatibant efficacy.
  • Angiotensin receptor blockers: similar risk of altered bradykinin activity.
  • Other bradykinin B2 antagonists: additive effects not studied.

Moderate Interactions (Monitor Closely)

  • Estrogen‑containing contraceptives: may affect frequency of HAE attacks.
  • Concurrent injectable biologics: monitor for overlapping injection‑site reactions.
  • Diuretics: observe blood pressure for possible hypotensive episodes.

Frequently Asked Questions

Icatibant acetate is indicated for the treatment of acute attacks of hereditary angioedema (HAE) in patients with C1‑inhibitor deficiency. It rapidly reduces swelling and associated symptoms during an HAE episode.

Icatibant is a competitive antagonist of the bradykinin B2 receptor. By binding to this receptor, it blocks the actions of bradykinin, preventing vasodilation and increased vascular permeability that cause the swelling characteristic of HAE attacks.

The dosing regimen for Icatibant is determined by the prescribing clinician based on the patient’s condition and regulatory guidelines. The medication is administered subcutaneously, and the prescriber decides the exact dose and timing.

The safety of icatibant in pregnancy and lactation has not been established. It should be used only if the potential benefit justifies the potential risk to the fetus or infant, and the decision should be made by a qualified healthcare professional.

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 logistics) and necessary import documentation.

Icatibant is a small‑molecule bradykinin B2 receptor antagonist, whereas other approved options such as C1‑inhibitor concentrates are plasma‑derived or recombinant proteins that replace the deficient inhibitor. Icatibant offers a rapid, subcutaneous route and targets the downstream mediator bradykinin directly.

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

The medication is supplied as a sterile solution for subcutaneous injection. The patient or a healthcare professional injects the prescribed dose into the subcutaneous tissue, typically in the abdomen or thigh, following aseptic technique.

Serious or rare adverse reactions can include anaphylaxis, severe hypersensitivity, angioedema, and significant hypotension. Immediate medical attention is required if any of these events occur.

Icatibant is contraindicated in individuals with known hypersensitivity to icatibant acetate or any of its excipients. Patients with such allergies should avoid the medication and seek alternative HAE therapies.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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