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 an injection solution for subcutaneous use. It treats acute attacks of hereditary angioedema in adults, including type I and type II forms of the disease.

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 a targeted therapy for hereditary angioedema, acting on the bradykinin pathway to relieve swelling.

  • Acute hereditary angioedema attacks: rapid reduction of swelling and pain in adults.
  • Hereditary angioedema type I: alleviates attack‑related edema when administered promptly.
  • Hereditary angioedema type II: provides fast symptom control during acute episodes.

How It Works

  • Icatibant selectively blocks the bradykinin B2 receptor, preventing bradykinin from binding and triggering vasodilation and increased vascular permeability. By inhibiting this receptor, the drug reduces the fluid extravasation that causes the characteristic swelling of hereditary angioedema, leading to rapid symptom relief after subcutaneous administration.

Side Effects

Icatibant may cause a range of adverse reactions, most of which are mild and transient.

Common Side Effects

  • Injection site pain: discomfort at the site of subcutaneous injection.
  • Redness or erythema: localized skin irritation.
  • Swelling at injection site: mild edema around the needle entry.
  • Nausea: occasional gastrointestinal upset.
  • Headache: mild to moderate head discomfort.
  • Dizziness: transient light‑headedness.

Serious or Rare Side Effects

  • Hypersensitivity reactions: rash, itching, or hives.
  • Anaphylaxis: severe allergic response requiring immediate medical attention.
  • Severe hypotension: marked drop in blood pressure.
  • Worsening angioedema: paradoxical increase in swelling.
  • Infection at injection site: signs of local infection.
  • Thrombocytopenia: low platelet count observed in rare cases.

Precautions & Warnings

Before using Icatibant, consider the following safety measures.

  • Pregnancy: safety not established; use only if benefit outweighs potential risk.
  • Breastfeeding: unknown effects; weigh risks and benefits before administration.
  • Renal impairment: exercise caution and monitor renal function.
  • Concomitant ACE inhibitors: monitor for increased bradykinin‑related angioedema.
  • Known hypersensitivity: discontinue immediately if allergic reaction occurs.
  • 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 levels or blood pressure.

Major Interactions (Avoid)

  • ACE inhibitors: may increase bradykinin, raising risk of angioedema.
  • Angiotensin receptor blockers: similar potential to elevate bradykinin.
  • Other bradykinin B2 antagonists: additive pharmacologic effect.

Moderate Interactions (Monitor Closely)

  • Diuretics: monitor blood pressure and electrolyte balance.
  • NSAIDs: may exacerbate edema or affect renal function.
  • Estrogen‑containing contraceptives: possible influence on HAE severity.
  • Antihistamines: may mask early signs of hypersensitivity.
  • Corticosteroids: monitor for overlapping immunomodulatory effects.

Frequently Asked Questions

Icatibant Universal Farma is indicated for the treatment of acute attacks of hereditary angioedema (HAE) in adult patients. It works by rapidly reducing swelling and associated pain during HAE episodes, providing prompt symptom relief.

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 mechanisms causing the swelling seen in hereditary angioedema.

The dose of icatibant is determined by the prescribing healthcare professional based on the patient’s clinical condition and regulatory guidelines. The prescriber will decide the exact amount and frequency of administration for each individual.

Safety data for icatibant in pregnancy and lactation are limited. It should only be used if the potential benefit justifies any possible risk to the fetus or infant, and the decision should be made by a qualified healthcare provider.

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‑esterase inhibitor concentrates and kallikrein inhibitors. Icatibant is administered subcutaneously and acts directly at the receptor level, offering rapid symptom control without the need for intravenous infusion.

Icatibant should be stored at 2‑8 °C in a refrigerator, protected from light. Do not freeze or shake the vial. If temporary temperature excursions occur, consult the product label for guidance before use.

Icatibant is given as a subcutaneous injection into the abdomen or thigh. The injection is performed by a trained healthcare professional or, in some cases, by the patient after proper instruction. The site should be rotated for repeated doses.

Serious risks include hypersensitivity reactions such as anaphylaxis, severe hypotension, and paradoxical worsening of angioedema. Patients should be monitored closely after administration, and any signs of severe allergic reaction require immediate medical attention.

Icatibant is contraindicated in patients with known hypersensitivity to icatibant or any of its excipients. Caution is also advised for individuals with severe renal impairment or those taking ACE inhibitors or ARBs without appropriate monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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