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

Icatibant Teva

Active Ingredient:
Icatibant Acetate
Origin:
EU

Icatibant Teva (Icatibant Acetate)

Icatibant, the active ingredient in Icatibant Teva, is a bradykinin B2 receptor antagonist presented as a solution for injection for subcutaneous use. It is indicated for the treatment of acute attacks of hereditary angioedema type I and type II in affected patients.

GNH India supplies Icatibant Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with distribution focused on the EU market. The company adheres to stringent quality standards and provides cold‑chain logistics for injectable products.

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

  • Icatibant is employed in the management of hereditary angioedema (HAE), a rare genetic disorder, by blocking the bradykinin pathway that causes rapid swelling of skin and mucosal tissues.
  • Hereditary angioedema type I: rapidly reduces swelling and pain during acute attacks.
  • Hereditary angioedema type II: alleviates symptoms of sudden edema episodes.
  • Hereditary angioedema (all types): provides prompt relief of airway and peripheral swelling.
  • Hereditary angioedema with airway involvement: helps prevent life‑threatening laryngeal edema during attacks.

How It Works

  • Icatibant selectively antagonizes the bradykinin B2 receptor on endothelial cells, preventing bradykinin from binding and activating the receptor. By blocking this interaction, the drug inhibits bradykinin‑mediated vasodilation, increased vascular permeability, and subsequent plasma extravasation that underlie the swelling seen in hereditary angioedema. The result is a rapid reduction of edema without affecting other vasoactive pathways.

Side Effects

The most frequently reported adverse reactions to Icatibant are related to its subcutaneous administration and its pharmacologic activity.

Common Side Effects

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

Serious or Rare Side Effects

  • Hypersensitivity reactions: rash, urticaria, or anaphylaxis.
  • Severe angioedema: worsening of swelling despite treatment.
  • Hypotension: marked drop in blood pressure.
  • Infection at injection site: cellulitis or abscess formation.

Precautions & Warnings

Before using Icatibant, clinicians should consider several safety aspects to minimize risk.

  • Renal impairment: monitor dosing as the drug is primarily eliminated renally.
  • Hepatic impairment: use with caution; limited data in severe liver disease.
  • Pregnancy: safety not established; prescribe only if benefit outweighs risk.
  • Breastfeeding: unknown excretion; consider alternative therapy.
  • Concomitant ACE inhibitors or ARBs: may increase risk of angioedema.
  • 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 levels or vascular tone.

Major Interactions (Avoid)

  • ACE inhibitors: additive bradykinin effect can precipitate angioedema.
  • Angiotensin receptor blockers: similar risk of increased bradykinin‑mediated swelling.
  • Other bradykinin B2 antagonists: no added therapeutic benefit and may increase adverse events.

Moderate Interactions (Monitor Closely)

  • Diuretics: may alter fluid balance and affect blood pressure.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): potential for heightened hypersensitivity.
  • Anticoagulants: monitor for bleeding if hypotension occurs.

Frequently Asked Questions

Icatibant Teva is indicated for the treatment of acute attacks of hereditary angioedema type I and type II. It works by rapidly reducing swelling of the skin, mucosa, and airway that can occur during an HAE episode.

Icatibant 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 drivers of the swelling seen in hereditary angioedema.

The dose and frequency of Icatibant Teva are determined by the prescribing clinician based on the patient’s condition and severity of the attack. It is administered as a subcutaneous injection, and the prescriber will provide specific instructions.

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 with 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 where required) and import documentation.

The primary alternative is plasma‑derived or recombinant C1‑esterase inhibitor replacement therapy. Icatibant offers a subcutaneous, self‑administered option that targets the bradykinin pathway directly, whereas C1‑esterase inhibitors replace the deficient protein and are given intravenously. Choice depends on patient preference, attack severity and clinical guidelines.

Icatibant Teva should be stored at 2‑8 °C (refrigerated). Keep the product in its original packaging, protect it from light, and do not freeze or shake the vial. If temperature excursions occur, consult the supplier before use.

Icatibant is supplied as a solution for injection and is given subcutaneously, typically into the abdomen or thigh. The injection is performed by a trained healthcare professional or, in some cases, by the patient after appropriate instruction.

Serious risks include hypersensitivity reactions such as rash, urticaria or anaphylaxis, worsening angioedema despite treatment, and significant hypotension. Patients should be monitored for these events, especially during the first administration.

Icatibant is contraindicated in patients with known hypersensitivity to icatibant or any of its excipients. Caution is also advised for individuals with severe renal or hepatic impairment, and for those taking ACE inhibitors or ARBs due to an increased risk of angioedema.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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