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

Icatibant Teva

Active Ingredient:
Icatibant Acetate
Origin:
EU

Icatibant Teva (Icatibant Acetate)

Icatibant acetate, the active ingredient in Icatibant Teva, is a bradykinin B2 receptor antagonist presented as a sterile subcutaneous injection solution for subcutaneous administration. It is indicated for the treatment of acute attacks of hereditary angioedema in adult patients, providing rapid symptom relief.

GNH India supplies Icatibant Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring quality‑controlled distribution across multiple markets.

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

  • Icatibant Teva is used to manage hereditary angioedema, a disorder driven by excessive bradykinin activity.
  • Hereditary angioedema type I: Reduces swelling by blocking bradykinin B2 receptors during acute episodes.
  • Hereditary angioedema type II: Provides rapid relief of symptoms by inhibiting bradykinin‑mediated vascular permeability.
  • Acute HAE attacks in adults: Offers prompt control of edema and associated discomfort.

How It Works

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

Side Effects

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

Common Side Effects

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

Serious or Rare Side Effects

  • Anaphylactic reaction: severe allergic response requiring immediate medical attention.
  • Severe hypotension: marked drop in blood pressure.
  • Angioedema unrelated to HAE: unexpected swelling in other body parts.
  • Urticaria: hives or skin rash.
  • Thrombocytopenia: low platelet count, monitored via blood tests.
  • Severe injection‑site infection: signs of cellulitis or abscess.

Precautions & Warnings

Before using Icatibant Teva, several safety considerations should be observed.

  • Confirm diagnosis: ensure the patient has hereditary angioedema before administration.
  • Allergy assessment: avoid use in individuals with known hypersensitivity to icatibant or excipients.
  • Pregnancy: prescribe only if the potential benefit justifies the potential risk to the fetus.
  • Breastfeeding: evaluate the risk‑benefit ratio before use in nursing mothers.
  • Concomitant ACE inhibitor therapy: monitor closely as combined effects on bradykinin may occur.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Icatibant Teva can interact with other medicines that influence bradykinin pathways or cardiovascular function.

Major Interactions (Avoid)

  • ACE inhibitors: may increase bradykinin levels and diminish icatibant efficacy.
  • C1‑esterase inhibitor prophylaxis: concurrent use can complicate assessment of therapeutic response.

Moderate Interactions (Monitor Closely)

  • Estrogen‑containing contraceptives: may affect frequency of HAE attacks.
  • Other B2 receptor antagonists: additive pharmacologic effects possible.
  • 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 associated symptoms during an HAE episode.

Icatibant acetate is a competitive 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 swelling in hereditary angioedema.

The specific dose and administration schedule are determined by the prescribing clinician based on the patient’s condition and clinical guidelines. Icatibant is administered as a subcutaneous injection under medical supervision.

Safety data in pregnancy and lactation are limited. The drug should be used only if the potential benefit justifies any 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 where required) and necessary import documentation.

Icatibant is a bradykinin B2 receptor antagonist, whereas other approved therapies such as C1‑esterase inhibitors replace a deficient protein. Icatibant offers a rapid, subcutaneous option for on‑demand treatment, while C1‑esterase inhibitors are often administered intravenously and may be used for both prophylaxis and acute attacks.

Icatibant Teva should be stored refrigerated between 2 °C and 8 °C. Keep the product in its original packaging, protect it from light, and do not freeze or shake the vial before use.

The medication is supplied as a sterile solution for subcutaneous injection. A single dose is typically given into the abdomen or thigh using a pre‑filled syringe or autoinjector, following the instructions provided by a healthcare professional.

Serious adverse reactions, although rare, include anaphylaxis, severe hypotension, unexpected angioedema unrelated to HAE, and severe injection‑site infections. Patients should be monitored closely after administration and seek immediate medical attention if any severe symptoms develop.

Icatibant Teva is contraindicated in individuals with known hypersensitivity to icatibant acetate or any component of the formulation. It should also be used with caution in patients receiving ACE inhibitors or other agents that affect bradykinin metabolism.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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