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 30 mg/0.3 mL prefilled syringe for subcutaneous use. It treats acute attacks of hereditary angioedema type I and type II in patients with a confirmed diagnosis and is indicated for rapid symptom control during life‑threatening swelling episodes.

GNH India supplies Icatibant Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies, clinics and other healthcare facilities worldwide, ensuring quality, regulatory compliance and reliable access to this specialty therapy for qualified providers.

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

  • Icatibant Teva is used to manage hereditary angioedema, a bradykinin‑mediated swelling disorder.
  • Hereditary angioedema type I: reduces severity and shortens duration of acute swelling attacks.
  • Hereditary angioedema type II: provides rapid relief of symptoms during acute episodes.
  • Hereditary angioedema attacks (any type): offers prompt control of edema and associated pain.

How It Works

  • Icatibant acetate selectively binds to the bradykinin B2 receptor on vascular endothelial cells, preventing bradykinin from activating the receptor. By blocking this pathway, it inhibits bradykinin‑induced vasodilation and increased vascular permeability, thereby reducing the formation of edema and associated pain during hereditary angioedema attacks.

Side Effects

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

Common Side Effects

  • Injection site pain: mild to moderate discomfort at the injection site.
  • Redness: localized erythema around the injection area.
  • Swelling: transient edema at the site of administration.
  • Nausea: occasional feeling of queasiness.

Serious or Rare Side Effects

  • Hypersensitivity reaction: rash, urticaria, or anaphylaxis requiring immediate medical attention.
  • Severe abdominal pain: persistent intense pain that may indicate a serious complication.
  • Thrombocytopenia: rare drop in platelet count observed in post‑marketing reports.

Precautions & Warnings

  • Before using Icatibant Teva, consider the following precautions.
  • Pregnancy: safety not established; use only if potential benefit justifies risk.
  • Breastfeeding: unknown; consider risk versus benefit.
  • Renal impairment: no dosage adjustment required, but monitor closely.
  • Concomitant ACE inhibitors: may increase bradykinin levels; observe for enhanced swelling.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Icatibant Teva can interact with other medicines; review the following categories.

Major Interactions (Avoid)

  • ACE inhibitors: additive bradykinin effect may worsen angioedema.
  • Angiotensin receptor blockers: similar risk of increased bradykinin.

Moderate Interactions (Monitor Closely)

  • Estrogen‑containing contraceptives: may increase frequency of HAE attacks; monitor.
  • Other B2 receptor antagonists: potential additive effect; observe response.
  • Immunosuppressants: no direct interaction but monitor infection risk.

Frequently Asked Questions

Icatibant Teva is indicated for the treatment of acute attacks of hereditary angioedema type I and type II. It provides rapid symptom relief by reducing swelling, pain, and potential airway obstruction associated with these life‑threatening episodes.

Icatibant acetate acts as 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 edema in hereditary angioedema.

The prescribed dose is determined by the treating physician based on the patient’s condition and clinical guidelines. In practice, a single 30 mg subcutaneous injection is commonly administered for an acute attack, but exact dosing and repeat administration are at the prescriber’s discretion.

Safety data for Icatibant acetate in pregnancy and lactation are limited. It should be used only if the potential benefit justifies any possible risk to the fetus or infant, and the decision should be made in consultation with a healthcare professional.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, cold‑chain shipping details and any necessary import documentation.

The primary alternative for hereditary angioedema is plasma‑derived or recombinant C1‑esterase inhibitor replacement. Icatibant works by blocking bradykinin receptors, offering a rapid, subcutaneous option, whereas C1‑esterase inhibitors replace the deficient protein and are administered intravenously. Choice depends on patient preference, attack severity and clinical response.

Icatibant Teva must be stored refrigerated at 2 °C to 8 °C. Keep the prefilled syringes in the original packaging, protect them from light, and avoid freezing or shaking the product. If temporary temperature excursions occur, consult the product label before use.

The medication is supplied as a prefilled syringe containing 30 mg of icatibant acetate in 0.3 mL. After cleaning the injection site, the syringe is inserted subcutaneously, typically into the abdomen or thigh, and the plunger is depressed to deliver the full dose. Patients should be observed for any immediate reactions.

Serious adverse events include hypersensitivity reactions such as rash, urticaria, or anaphylaxis, severe abdominal pain, and rare cases of thrombocytopenia. Any signs of a severe allergic response or unexplained intense pain should prompt immediate medical evaluation.

Icatibant Teva is contraindicated in individuals with known hypersensitivity to icatibant acetate or any of the formulation excipients. Caution is also advised for patients with a history of severe allergic reactions, and it should be used under medical supervision in those with uncontrolled cardiovascular disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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