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

Icatibant Teva

Active Ingredient:
Icatibant
Origin:
EU

Icatibant Teva (Icatibant)

Icatibant, the active ingredient in Icatibant Teva, is a bradykinin B2 receptor antagonist presented as an injectable solution for subcutaneous use. It is indicated for the treatment of acute attacks of hereditary angioedema type I and type II in patients who experience rapid swelling of the skin, gastrointestinal tract, or airway.

GNH India supplies Icatibant Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory‑approved batches for global distribution.

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

  • Icatibant is used to treat hereditary angioedema by targeting the bradykinin pathway.
  • Hereditary angioedema type I: administration of Icatibant leads to rapid reversal of edema by blocking bradykinin‑mediated vascular leakage, thereby reducing swelling of the skin, gastrointestinal tract and airway within minutes to hours.
  • Hereditary angioedema type II: the drug similarly antagonizes bradykinin B2 receptors, providing prompt relief of swelling episodes and improving airway patency and abdominal discomfort during acute attacks.

How It Works

  • Icatibant is a synthetic decapeptide that competitively binds to the bradykinin B2 receptor on endothelial cells. By occupying the receptor, it prevents endogenous bradykinin from activating the signaling cascade that causes vasodilation and increased vascular permeability. The inhibition of this pathway stops the formation of excess plasma leakage that underlies the swelling seen in hereditary angioedema, allowing the acute edema to resolve more quickly.

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 site of subcutaneous administration.
  • Erythema: redness around the injection area.
  • Local swelling: mild edema at the injection site.
  • Pruritus: itching at or near the injection site.
  • Nausea: occasional gastrointestinal upset.
  • Headache: mild to moderate head pain.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Angioedema of the face or throat: potentially life‑threatening swelling.
  • Hypotension: sudden drop in blood pressure.
  • Severe hypersensitivity: widespread rash or hives.
  • Rare thrombotic events: clot formation in blood vessels.

Precautions & Warnings

  • When using Icatibant, several safety considerations should be observed to minimize risk.
  • Allergy assessment: verify no known hypersensitivity to Icatibant or its excipients.
  • Pregnancy: safety has not been established; use only if potential benefit outweighs risk.
  • Breastfeeding: unknown safety; caution advised.
  • Renal impairment: consider dose adjustment and monitor response.
  • Concomitant ACE inhibitor therapy: increased bradykinin levels may heighten risk of angioedema; monitor closely.
  • 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 system or affect hemodynamic stability.

Major Interactions (Avoid)

  • ACE inhibitors: may amplify bradykinin‑mediated angioedema.
  • Neprilysin inhibitors (e.g., sacubitril): increase bradykinin levels, raising risk of swelling.
  • Other bradykinin B2 receptor agonists: antagonistic competition can reduce efficacy.

Moderate Interactions (Monitor Closely)

  • Estrogen‑containing oral contraceptives: may modestly increase angioedema risk.
  • Other HAE therapies (e.g., C1‑esterase inhibitor concentrates): overlapping effects on edema control.
  • NSAIDs: potential to exacerbate hypersensitivity reactions.
  • Diuretics: may affect fluid balance and blood pressure, requiring observation.

Frequently Asked Questions

Icatibant Teva is indicated for the treatment of acute attacks of hereditary angioedema (HAE) type I and type II. It helps to rapidly reduce swelling of the skin, gastrointestinal tract, and airway that can occur during these episodes.

Icatibant is a synthetic peptide that competitively blocks the bradykinin B2 receptor on endothelial cells. By preventing bradykinin from binding, it stops the cascade that causes vasodilation and increased vascular permeability, thereby limiting the edema characteristic of HAE.

The dosing regimen for Icatibant is determined by the prescribing clinician. Typically, a single subcutaneous injection is given at the onset of an HAE attack, with additional doses allowed according to the product label and patient response.

Safety data for Icatibant in pregnancy and lactation are limited. It should be used only if the potential benefit justifies the potential 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 with the required quantity. GNH India supplies 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 for HAE is a C1‑esterase inhibitor concentrate, which replaces the deficient protein. Icatibant, by contrast, blocks the downstream bradykinin B2 receptor. Both provide rapid symptom relief, but Icatibant is a small‑molecule injection that does not require plasma‑derived products.

Icatibant should be stored at 2 °C to 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 given as a subcutaneous injection, usually into the abdomen or thigh, using a pre‑filled syringe. The injection is performed by a trained healthcare professional or, in some cases, by the patient after appropriate instruction.

Serious risks include anaphylaxis, severe hypersensitivity reactions, angioedema of the face or throat that can compromise the airway, and sudden hypotension. Patients should be monitored closely after the first dose and instructed to seek immediate medical help if these symptoms develop.

Icatibant is contraindicated in individuals with known hypersensitivity to the drug or any of its excipients. Caution is also advised for patients taking ACE inhibitors or other agents that increase bradykinin levels, as they may have an elevated risk of angioedema.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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