Product image of Icatibant Generics (Uk) (Icatibant) supplied by GNH India

Icatibant Generics (Uk)

Active Ingredient:
Icatibant
Origin:
EU

Icatibant Generics (Uk) (Icatibant)

Icatibant, the active ingredient in Icatibant Generics (Uk), is a Bradykinin B2 receptor antagonist presented as a solution for injection for subcutaneous use. It treats acute attacks of hereditary angioedema type I and type II in patients who experience rapid swelling of the skin, gastrointestinal tract, or airway.

GNH India supplies Icatibant Generics (Uk) as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with a focus on quality assurance and regulatory compliance to meet global demand.

Manufacturer / TM Owner

Generics [uk] Limited

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Indications & Clinical Uses

Icatibant is used to treat hereditary angioedema by targeting the bradykinin pathway.

  • Hereditary angioedema type I: provides rapid reduction of swelling and pain during acute attacks.
  • Hereditary angioedema type II: delivers swift control of edema and associated discomfort in acute episodes.
  • Bradykinin‑mediated angioedema: alleviates symptoms by blocking bradykinin effects that cause vascular leakage.

How It Works

  • Icatibant selectively binds to the bradykinin B2 receptor on vascular endothelial cells, preventing bradykinin from activating the receptor. By blocking this interaction, the drug inhibits bradykinin‑induced vasodilation and increased vascular permeability, thereby reducing the fluid leakage that causes swelling in hereditary angioedema attacks. The antagonism is rapid and reversible, allowing prompt symptom control after subcutaneous administration.

Side Effects

Icatibant may cause a range of adverse reactions, most of which are related to its injection route or pharmacologic activity.

Common Side Effects

  • Injection site pain: mild to moderate discomfort at the injection site.
  • Redness at injection site: localized erythema.
  • Swelling at injection site: transient edema.
  • Nausea: occasional feeling of queasiness.
  • Headache: mild to moderate head pain.
  • Dizziness: brief sensation of light‑headedness.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Severe hypotension: marked drop in blood pressure.
  • Angioedema paradoxical: unexpected swelling despite treatment.
  • Urticaria: widespread hives.
  • Thrombocytopenia: low platelet count.
  • Severe injection site reaction: necrosis or infection.

Precautions & Warnings

When using Icatibant, several safety considerations should be observed to minimize risk.

  • Pregnancy: safety not established; avoid unless clearly needed.
  • Breastfeeding: unknown safety; weigh benefits against potential risks.
  • Renal impairment: use with caution; monitor renal function.
  • Concomitant ACE inhibitors: may increase bradykinin levels; observe for enhanced edema.
  • Hypersensitivity: discontinue if signs of allergic reaction appear.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Icatibant can interact with other medicines that influence the bradykinin system or cardiovascular function.

Major Interactions (Avoid)

  • ACE inhibitors: may raise bradykinin levels and increase risk of angioedema.
  • Angiotensin receptor blockers: similar potential to augment bradykinin‑mediated effects.

Moderate Interactions (Monitor Closely)

  • Diuretics: monitor blood pressure and electrolyte balance.
  • Other bradykinin antagonists: additive pharmacologic effect may require dose adjustment.
  • NSAIDs: may affect edema control and renal function.

Frequently Asked Questions

Icatibant is indicated for the treatment of acute attacks of hereditary angioedema (HAE) types I and II. By blocking the bradykinin B2 receptor, it rapidly reduces swelling of the skin, gastrointestinal tract, and airway that occurs during an HAE episode.

Icatibant works as a selective antagonist of the bradykinin B2 receptor. It prevents bradykinin from binding to this receptor on vascular endothelial cells, thereby inhibiting the vasodilation and increased vascular permeability that lead to the fluid leakage responsible for angioedema.

The dose of Icatibant is determined by the prescribing clinician. Typically, a single subcutaneous injection is administered at the onset of an acute HAE attack, and additional doses may be given based on clinical response. Patients should follow the prescriber’s exact instructions and not adjust the dose on their own.

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 order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, and will request trade or institutional credentials. The team then replies with pricing, availability, shipping details (including cold‑chain handling if required) and any necessary import documentation.

The primary alternative for acute HAE is a plasma‑derived C1‑esterase inhibitor (e.g., Berinert). Icatibant offers a subcutaneous, self‑administered option that works by blocking bradykinin, whereas C1‑esterase inhibitors replace the deficient protein and are given intravenously. Choice depends on patient preference, speed of onset, and clinical response.

Icatibant should be stored at 2‑8 °C (refrigerated). Keep the vial in its original packaging, protect it from light, and avoid freezing or shaking. If temporary storage at room temperature is unavoidable, limit exposure to no more than 30 °C for a short period.

Icatibant is given as a subcutaneous injection, usually into the abdomen or thigh. The injection site should be cleaned with an alcohol swab, and the solution administered using the supplied pre‑filled syringe. Patients are advised to rotate injection sites and monitor for local reactions.

Serious risks include anaphylaxis, severe hypotension, and paradoxical angioedema that can worsen swelling despite treatment. Any signs of severe allergic reaction, sudden drop in blood pressure, or unexpected swelling should prompt immediate medical attention.

Icatibant is contraindicated in individuals with known hypersensitivity to the active substance or any of the excipients. Caution is also advised for patients with severe renal impairment or those receiving ACE inhibitors or ARBs, as the risk of bradykinin‑related adverse events may be increased.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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