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 30 mg/0.3 mL solution for injection for subcutaneous use. It treats hereditary angioedema caused by C1‑inhibitor deficiency in patients who need rapid relief of acute swelling episodes.

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 indicated for the treatment of hereditary angioedema, a bradykinin‑mediated angioedema disorder.

  • Hereditary angioedema (C1‑inhibitor deficiency) – acute attacks: Provides rapid reduction of swelling and associated pain.
  • Hereditary angioedema (C1‑inhibitor deficiency) – adult patients: Enables on‑demand subcutaneous self‑administration.
  • Hereditary angioedema (C1‑inhibitor deficiency) – type I and II: Effective in both subtypes for acute symptom control.

How It Works

  • Icatibant acts as a selective competitive antagonist at the bradykinin B2 receptor. By binding to this receptor, it blocks the actions of bradykinin, preventing the vasodilation and increased vascular permeability that lead to the swelling characteristic of hereditary angioedema. This inhibition results in a rapid decrease in edema during acute attacks.

Side Effects

Icatibant may cause a range of adverse reactions, most of which are related to its subcutaneous administration and pharmacologic activity.

Common Side Effects

  • Injection site pain: Discomfort at the site of subcutaneous injection.
  • Redness or erythema: Localized skin reddening.
  • Swelling at injection site: Mild to moderate edema.
  • Nausea: Transient gastrointestinal upset.
  • Headache: Mild to moderate intensity.

Serious or Rare Side Effects

  • Anaphylaxis: Severe allergic reaction requiring immediate medical attention.
  • Hypotension: Significant drop in blood pressure.
  • Laryngeal edema: Swelling of the throat that may compromise airway.
  • Severe urticaria: Widespread hives.
  • Angioedema unrelated to HAE: Unexpected swelling in other body parts.

Precautions & Warnings

When using Icatibant, certain safety considerations should be observed.

  • Renal impairment: Use with caution and monitor renal function.
  • Hepatic impairment: Adjust therapy if liver function is compromised.
  • Pregnancy: Safety not established; avoid unless benefit outweighs risk.
  • Breastfeeding: Unknown safety; consider potential risks.
  • Concomitant ACE inhibitors: May increase bradykinin levels; 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 bradykinin pathways or vascular tone.

Major Interactions (Avoid)

  • ACE inhibitors: May potentiate bradykinin‑mediated angioedema.
  • Angiotensin receptor blockers: Similar risk of enhanced bradykinin effects.
  • Nitrates: Additive vasodilatory effect leading to hypotension.

Moderate Interactions (Monitor Closely)

  • Estrogen‑containing oral contraceptives: May increase frequency of HAE attacks.
  • Diuretics: Can affect fluid balance and blood pressure.

Frequently Asked Questions

Icatibant Teva is used to treat acute attacks of hereditary angioedema (HAE) caused by C1‑inhibitor deficiency. It works by rapidly reducing swelling and associated pain during an HAE episode, providing on‑demand relief for patients.

Icatibant is a selective competitive antagonist of the bradykinin B2 receptor. By blocking this receptor, it prevents bradykinin‑induced vasodilation and increased vascular permeability, which are the primary mechanisms that cause the swelling seen in hereditary angioedema.

The dose of Icatibant Teva is determined by the prescribing healthcare professional based on the patient’s condition and clinical guidelines. The product is supplied as a 30 mg/0.3 mL solution for subcutaneous injection, and the prescriber will specify the exact dosing regimen.

Safety of Icatibant in pregnancy and lactation has not been established. It should be used only if the potential benefit justifies the potential risk to the fetus or infant, and the decision should be made by a qualified healthcare provider.

To order Icatibant Teva, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, and will request verification of trade or institutional credentials before providing pricing, availability, shipping details (including cold‑chain if needed) and import documentation.

Icatibant is a bradykinin B2 receptor antagonist, whereas other HAE therapies such as C1‑esterase inhibitor concentrates replace the deficient protein. Icatibant offers a rapid, subcutaneous, on‑demand option that does not require intravenous administration, making it convenient for self‑treatment during acute attacks.

Icatibant Teva should be stored at 2–8 °C in a refrigerator. Keep the product in its original packaging, protect it from light, and do not freeze or shake the vial. If temporary temperature excursions occur, follow the manufacturer’s guidance before use.

Icatibant Teva is administered as a subcutaneous injection. The 30 mg/0.3 mL solution is injected into the abdominal wall or thigh using a sterile needle, typically by the patient or a caregiver after proper training from a healthcare professional.

The most serious risks include severe allergic reactions such as anaphylaxis, significant hypotension, and laryngeal edema that can compromise the airway. Patients should be monitored for these events, and immediate medical attention is required if they occur.

Icatibant is contraindicated in individuals with known hypersensitivity to icatibant or any of its excipients. Patients taking ACE inhibitors or angiotensin receptor blockers should avoid concurrent use due to the increased risk of angioedema, unless specifically directed by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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