Product image of Icatibant Zentiva (Icatibant Acetate) supplied by GNH India

Icatibant Zentiva

Active Ingredient:
Icatibant Acetate
Origin:
EU

Icatibant Zentiva (Icatibant Acetate)

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

Manufacturer / TM Owner

Zentiva, K.S.

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Indications & Clinical Uses

Icatibant Zentiva acts on the bradykinin pathway to relieve acute hereditary angioedema episodes.

  • Hereditary angioedema type I: reduces the severity and duration of acute attacks.
  • Hereditary angioedema type II: provides rapid symptom relief during flare‑ups.
  • Hereditary angioedema with normal C1‑INH: alleviates swelling by blocking bradykinin‑mediated vascular leakage.

How It Works

  • Icatibant acetate competitively blocks the bradykinin B2 receptor on vascular endothelial cells, preventing bradykinin from inducing vasodilation and increased vascular permeability. By inhibiting this receptor, the drug curtails the cascade that leads to the rapid swelling characteristic of hereditary angioedema attacks.

Side Effects

Icatibant Zentiva may cause a range of adverse reactions following subcutaneous injection.

Common Side Effects

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

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Severe hypersensitivity: rash, itching, or swelling beyond the injection site.
  • Angioedema: unexpected swelling of lips, tongue, or throat.
  • Hypotension: sudden drop in blood pressure.
  • Thrombocytopenia: reduced platelet count.
  • Injection‑site infection: signs of local infection such as warmth, pus, or fever.

Precautions & Warnings

Before using Icatibant Zentiva, consider the following safety measures.

  • Pregnancy: consult a healthcare professional; safety data are limited.
  • Breastfeeding: weigh potential risks and benefits with a clinician.
  • Renal impairment: use with caution; monitor renal function.
  • Concomitant ACE inhibitors or neprilysin inhibitors: monitor for enhanced bradykinin effects.
  • History of hypersensitivity to icatibant or excipients: avoid use.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Icatibant Zentiva can interact with other medicines that influence bradykinin pathways or hemodynamics.

Major Interactions (Avoid)

  • ACE inhibitors: may increase bradykinin levels and risk of angioedema.
  • Neprilysin inhibitors: can potentiate bradykinin‑mediated effects.
  • Estrogen‑containing therapies: may exacerbate hereditary angioedema symptoms.

Moderate Interactions (Monitor Closely)

  • NSAIDs: watch for additive swelling or pain at injection sites.
  • Diuretics: monitor blood pressure and electrolyte balance during therapy.

Frequently Asked Questions

Icatibant Zentiva is used to treat acute attacks of hereditary angioedema (HAE). It works by rapidly reducing swelling and pain associated with HAE episodes, providing relief for patients who experience sudden, potentially life‑threatening swelling of the skin, gastrointestinal tract, or airway.

Icatibant acetate is a selective antagonist of the bradykinin B2 receptor. By blocking this receptor, it prevents bradykinin‑induced vasodilation and increased vascular permeability, which are the primary mechanisms causing the rapid swelling seen in hereditary angioedema attacks.

The dosage of Icatibant Zentiva is determined by the prescribing clinician based on the patient’s condition, weight, and severity of the HAE attack. The prescriber will specify the exact amount, frequency, and duration of treatment.

Safety data for icatibant acetate in pregnancy and lactation are limited. Healthcare providers should evaluate the potential benefits against any possible risks before prescribing it to pregnant or breastfeeding individuals.

To place an order, submit an enquiry on the product page at gnhindia.com, indicating 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 any required import documentation.

Icatibant Zentiva is a bradykinin B2 receptor antagonist, whereas other HAE therapies may target C1‑esterase inhibitor replacement or kallikrein inhibition. Icatibant offers a subcutaneous, rapid‑acting option that directly blocks bradykinin, making it useful for patients who prefer self‑administration and need quick symptom control.

Icatibant Zentiva should be stored at 2‑8 °C (refrigerated). Keep the product in its original packaging, protect it from light, and avoid freezing or shaking the vial. Do not use the medication if it has been exposed to temperatures outside the recommended range.

The medication is supplied as a sterile injection solution for subcutaneous use. A healthcare professional or trained patient injects the prescribed dose into the subcutaneous tissue, typically in the abdomen or thigh, following aseptic technique and the instructions provided by the prescriber.

Serious risks include anaphylaxis, severe hypersensitivity reactions, unexpected angioedema of the face or airway, and sudden hypotension. Patients should be monitored closely after injection, and any signs of severe allergic reaction or rapid swelling should prompt immediate medical attention.

Icatibant Zentiva is contraindicated in individuals with known hypersensitivity to icatibant acetate or any of the formulation excipients. Patients with a history of severe allergic reactions to bradykinin B2 antagonists should avoid its use.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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