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 hereditary angioedema attacks in patients with confirmed HAE and is formulated for rapid subcutaneous administration to quickly alleviate swelling.

GNH India supplies Icatibant Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring reliable cold‑chain logistics and regulatory compliance for global distribution.

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

  • Icatibant is used to manage hereditary angioedema, a disorder characterized by excessive bradykinin‑mediated swelling.
  • Hereditary angioedema (HAE) type I: reduces swelling and relieves symptoms during acute episodes.
  • Hereditary angioedema (HAE) type II: blocks bradykinin‑induced edema to control attacks.
  • Hereditary angioedema with normal C1‑INH (HAE‑nC1‑INH): provides rapid symptom control in acute attacks.

How It Works

  • Icatibant selectively antagonizes the bradykinin B2 receptor on vascular endothelial cells, preventing bradykinin from binding and triggering vasodilation and increased vascular permeability. By blocking this pathway, the drug curtails the cascade that leads to fluid extravasation and tissue swelling characteristic of hereditary angioedema attacks.

Side Effects

Icatibant may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Injection site pain or erythema.
  • Localized swelling at the injection site.
  • Nausea or mild headache.
  • Dizziness or transient fatigue.

Serious or Rare Side Effects

  • Hypersensitivity reactions including anaphylaxis.
  • Severe hypotension or cardiovascular collapse.
  • Worsening angioedema or new onset of facial swelling.

Precautions & Warnings

  • When prescribing Icatibant, clinicians should observe several safety considerations.
  • Hypersensitivity assessment: verify no known allergy to icatibant or formulation components.
  • Monitor for worsening angioedema: observe patient after injection for any increase in swelling.
  • Cardiovascular caution: use carefully in patients with hypotension or cardiac disease.
  • Concurrent bradykinin‑modulating drugs: avoid co‑administration with ACE inhibitors or other B2 antagonists.
  • 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 pathway or affect injection site absorption.

Major Interactions (Avoid)

  • ACE inhibitors: may increase bradykinin levels and exacerbate angioedema.
  • Concurrent use of other bradykinin B2 receptor antagonists: additive blockade can lead to unpredictable effects.

Moderate Interactions (Monitor Closely)

  • Subcutaneous co‑injections (e.g., insulin): may alter absorption kinetics; monitor efficacy.
  • Immunosuppressive agents: watch for heightened infection risk.
  • Anticoagulants (e.g., warfarin): monitor for any changes in bleeding tendency.

Frequently Asked Questions

Icatibant Teva is indicated for the acute treatment of hereditary angioedema (HAE) attacks in patients with confirmed HAE. It works by rapidly reducing swelling and alleviating the painful symptoms associated with these episodes.

Icatibant is a selective antagonist of the bradykinin B2 receptor. By blocking this receptor, it prevents bradykinin‑mediated 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. It is administered as a subcutaneous injection, and the exact regimen should be confirmed with the treating physician.

Safety data for icatibant in pregnancy and lactation are limited. It should only be used if the potential benefit justifies any potential risk to the fetus or infant, and the decision must 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 handling), and any necessary import documentation.

The primary alternative for HAE attacks is plasma‑derived C1‑esterase inhibitor replacement therapy. Icatibant offers a subcutaneous, self‑administered option that directly blocks bradykinin, whereas C1‑esterase inhibitors replace the deficient protein. Choice depends on patient preference, attack severity, and clinical response.

Icatibant Teva must be stored refrigerated at 2‑8 °C. Keep the product in its original packaging, protect it from light, and avoid freezing or shaking the vial. If temporary temperature excursions occur, consult the supplier before use.

Icatibant is given as a single subcutaneous injection into the abdomen, thigh, or upper arm. The injection site should be rotated for repeated doses, and patients should be instructed on proper aseptic technique and disposal of sharps according to local regulations.

Serious adverse events include hypersensitivity reactions such as anaphylaxis, severe hypotension, and worsening angioedema that may involve the airway. Immediate medical attention is required if any of these symptoms develop after administration.

Icatibant is contraindicated in individuals with known hypersensitivity to icatibant acetate or any excipients in the formulation. It should also be avoided in patients receiving other bradykinin B2 receptor antagonists or ACE inhibitors when alternative therapies are available.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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