Product image of Icatibant Universal Farma (Icatibant) supplied by GNH India

Icatibant Universal Farma

Active Ingredient:
Icatibant
Origin:
EU

Icatibant Universal Farma (Icatibant)

Icatibant, the active ingredient in Icatibant Universal Farma, is a Bradykinin B2 receptor antagonist presented as a subcutaneous injection for subcutaneous use. It treats acute attacks of hereditary angioedema in patients with confirmed HAE.

GNH India supplies Icatibant Universal Farma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Universal Farma, S.L.

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Indications & Clinical Uses

Icatibant is used to treat conditions mediated by excessive bradykinin activity, primarily hereditary angioedema.

  • Hereditary angioedema type I: Provides rapid relief of acute swelling episodes in patients with C1‑inhibitor deficiency.
  • Hereditary angioedema type II: Reduces edema and associated pain during acute attacks in patients with dysfunctional C1‑inhibitor.
  • Hereditary angioedema with normal C1‑inhibitor (HAE‑nC1‑INH): Controls sudden swelling attacks in patients with genetically confirmed HAE‑nC1‑INH.

How It Works

  • Icatibant selectively blocks the bradykinin B2 receptor, preventing bradykinin from binding and activating the receptor. This inhibition stops bradykinin‑induced vasodilation and increased vascular permeability, thereby reducing the fluid leakage and swelling that characterize hereditary angioedema attacks.

Side Effects

Icatibant may cause a range of adverse reactions, most of which are related to the injection site or systemic response.

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 local edema.
  • Nausea: occasional gastrointestinal upset.
  • Headache: mild to moderate intensity.
  • Dizziness: transient light‑headedness.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Severe hypotension: sudden drop in blood pressure.
  • Angioedema unrelated to HAE: unexpected swelling in other body parts.
  • Urticaria: widespread hives.
  • Severe injection‑site necrosis: tissue damage at the site.
  • Life‑threatening allergic reactions: including bronchospasm or throat swelling.

Precautions & Warnings

Before using Icatibant, clinicians should consider several safety measures.

  • Confirm diagnosis: verify hereditary angioedema type before administration.
  • Monitor for hypersensitivity: observe patients for signs of allergic reaction after injection.
  • Evaluate cardiovascular status: caution in patients with unstable blood pressure.
  • Review concomitant medications: avoid concurrent use of ACE inhibitors when possible.
  • Pregnancy and lactation: assess risk‑benefit ratio; limited data are available.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

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

Major Interactions (Avoid)

  • ACE inhibitors: increase bradykinin levels, potentially reducing Icatibant efficacy.
  • Estrogen‑containing contraceptives: may exacerbate angioedema frequency.
  • Other bradykinin antagonists: concurrent use may lead to unpredictable effects.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may increase risk of gastrointestinal irritation.
  • Diuretics: monitor blood pressure and electrolyte balance.
  • Beta‑blockers: observe for altered cardiovascular response.
  • Antihistamines: may mask early signs of allergic reactions.

Frequently Asked Questions

Icatibant Universal Farma is indicated for the treatment of acute attacks of hereditary angioedema (HAE) in patients with confirmed HAE. It works by rapidly reducing swelling and associated symptoms during an HAE episode.

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 prescribed dose of Icatibant is determined by the treating physician based on the patient’s clinical condition and regulatory guidelines. Dosing instructions are provided on the prescription label and should not be altered without medical advice.

Safety data for Icatibant in pregnancy and lactation are limited. Prescribers should weigh the potential benefits against any possible risks and consider alternative therapies when appropriate.

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 if needed) and import documentation.

Icatibant is a bradykinin B2 receptor antagonist, whereas other approved HAE therapies include C1‑inhibitor concentrates and kallikrein inhibitors. Icatibant offers a subcutaneous route and rapid onset, making it convenient for self‑administration during acute attacks.

Icatibant should be stored at 2‑8 °C in a refrigerator, protected from light, and must not be frozen or shaken. Keep the product in its original packaging until use to maintain stability.

Icatibant is given by subcutaneous injection, typically into the abdomen or thigh. The injection is performed by a trained healthcare professional or by the patient after appropriate instruction.

Serious risks include anaphylaxis, severe hypotension, and unexpected angioedema unrelated to HAE. Patients should be monitored closely after the first dose and instructed to seek immediate medical help if any severe reaction occurs.

Icatibant is contraindicated in patients with known hypersensitivity to the drug or any of its excipients. Caution is also advised for individuals taking ACE inhibitors or estrogen‑containing products, as these may increase the risk of adverse events.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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