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 treats acute attacks of hereditary angioedema in adult patients, providing rapid relief by blocking bradykinin‑mediated vascular permeability and swelling.

GNH India supplies Icatibant Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

Icatibant is used to manage hereditary angioedema (HAE) attacks, a bradykinin‑mediated condition affecting the vascular system.

  • Hereditary angioedema type I: reduces swelling and pain during acute attacks.
  • Hereditary angioedema type II: provides rapid symptom relief in episodes.
  • Hereditary angioedema with C1‑inhibitor deficiency: alleviates attack severity in adults.

How It Works

  • Icatibant acts as a competitive antagonist at the bradykinin B2 receptor. By binding to this receptor, it blocks the action of bradykinin, a peptide that causes vasodilation and increased vascular permeability. The inhibition prevents the cascade that leads to the rapid swelling characteristic of hereditary angioedema, thereby limiting attack duration and severity.

Side Effects

Icatibant may cause a range of adverse reactions, most of which are related to the injection site or systemic exposure.

Common Side Effects

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

Serious or Rare Side Effects

  • Hypersensitivity reactions: rash, urticaria, or angioedema.
  • Anaphylaxis: severe, potentially life‑threatening allergic response.
  • Severe hypotension: marked drop in blood pressure requiring medical attention.
  • Thrombocytopenia: low platelet count observed in rare cases.
  • Acute pulmonary edema: rare respiratory compromise.

Precautions & Warnings

Before using Icatibant, consider the following safety measures.

  • Pregnancy: safety not established; avoid unless clearly needed.
  • Breastfeeding: unknown effects; weigh benefits against potential risks.
  • Renal impairment: use with caution; monitor renal function.
  • History of hypersensitivity: avoid if previous allergic reaction to icatibant.
  • Concomitant ACE inhibitors: monitor for increased bradykinin‑related effects.
  • 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 bradykinin pathways or hemodynamics.

Major Interactions (Avoid)

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

Moderate Interactions (Monitor Closely)

  • C1‑inhibitor concentrates: concurrent use may affect therapeutic response.
  • Other bradykinin antagonists: additive inhibition could alter efficacy.
  • Diuretics: monitor blood pressure and electrolyte balance during therapy.

Frequently Asked Questions

Icatibant Teva is indicated for the treatment of acute attacks of hereditary angioedema (HAE) in adult patients. It works by rapidly reducing swelling and pain associated with HAE episodes, providing timely symptom relief.

Icatibant is a competitive antagonist of the bradykinin B2 receptor. By blocking this receptor, it prevents bradykinin from causing vasodilation and increased vascular permeability, which are the primary drivers of swelling in hereditary angioedema.

The dose of Icatibant Teva is determined by the prescribing clinician based on the patient’s condition and regulatory guidelines. The prescriber will specify the exact amount and frequency appropriate for each individual.

Safety of icatibant in pregnancy and lactation has not been established. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the decision must 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 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.

Icatibant is a bradykinin B2 receptor antagonist, whereas other approved HAE therapies include C1‑inhibitor concentrates and kallikrein inhibitors. Icatibant offers a subcutaneous route and rapid onset, making it suitable for patients who prefer self‑administration over intravenous options.

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

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

Serious risks include hypersensitivity reactions such as rash, urticaria, anaphylaxis, severe hypotension, and rare cases of thrombocytopenia. Patients should be monitored for any signs of allergic response or sudden blood pressure changes after administration.

Icatibant is contraindicated in individuals with known hypersensitivity to icatibant or any of its excipients. Caution is also advised for patients with severe renal impairment or those receiving ACE inhibitors or ARBs without appropriate monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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