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 injectable formulation for injection use. It is employed to treat acute hereditary angioedema attacks in patients with confirmed HAE type I or II, providing rapid relief of swelling and associated pain.

GNH India supplies Icatibant Universal Farma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, adhering to EU quality standards and providing reliable cold‑chain logistics for injectable biologics. Our distribution network spans Europe, Asia, Africa and the Americas, ensuring timely access to this essential therapy.

Manufacturer / TM Owner

Universal Farma, S.L.

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Indications & Clinical Uses

Icatibant is used to manage bradykinin‑mediated hereditary angioedema attacks, providing rapid symptom control.

  • Hereditary angioedema attacks: reduces swelling and pain during acute episodes.
  • Hereditary angioedema type I: provides rapid relief of airway and peripheral edema.
  • Hereditary angioedema type II: blocks bradykinin effects to prevent progression of attacks.

How It Works

  • Icatibant acts as a competitive antagonist at the bradykinin B2 receptor. By binding to this receptor, it blocks the actions of endogenous bradykinin, preventing vasodilation and increased vascular permeability that cause the swelling characteristic of hereditary angioedema. This inhibition leads to a rapid reduction of edema and associated discomfort.

Side Effects

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

Common Side Effects

  • Injection site pain: mild to moderate discomfort at the injection site.
  • Erythema: localized redness around the injection area.
  • Nausea: occasional feeling of queasiness.
  • Headache: transient mild headache.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Severe hypersensitivity reactions: including angioedema at sites other than the injection area.
  • Hypotension: sudden drop in blood pressure that may cause dizziness or fainting.

Precautions & Warnings

Before using Icatibant, consider the following safety measures.

  • Pregnancy: safety not established; use only if potential benefit justifies the risk.
  • Breastfeeding: unknown effects; weigh benefits against possible risks.
  • Renal impairment: no dosage adjustment required, but monitor for adverse events.
  • 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 affect bradykinin pathways or hemodynamics.

Major Interactions (Avoid)

  • ACE inhibitors: may elevate bradykinin levels, increasing risk of angioedema.
  • Estrogen‑containing contraceptives: can potentiate bradykinin‑mediated swelling.
  • Other bradykinin B2 antagonists: additive pharmacologic effect may lead to excessive blockade.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may exacerbate gastrointestinal irritation.
  • Diuretics: could influence fluid balance and blood pressure.
  • Corticosteroids: may alter immune response and affect infection risk.

Frequently Asked Questions

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

Icatibant is a competitive antagonist of the bradykinin B2 receptor. By blocking this receptor, it prevents bradykinin‑induced vasodilation and increased vascular permeability, which are the primary drivers of swelling 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 required for each acute HAE episode.

Safety data for icatibant in pregnancy and lactation are limited. It should only be used if the potential benefit to the mother outweighs 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 handling if needed) and any required 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 provides rapid symptom relief, while the alternatives may be given intravenously or have different mechanisms of action.

Icatibant should be stored at 2‑8 °C (refrigerated). Keep the product in its original packaging, protect it from light, and avoid freezing or shaking the vial. Do not use the medication if it has been exposed to temperatures outside the recommended range.

Icatibant is supplied as a sterile solution for subcutaneous injection. The prescribed dose is injected into the abdominal wall or thigh using a pre‑filled syringe or autoinjector, following the instructions provided by the healthcare professional.

The most serious risks include severe hypersensitivity reactions such as anaphylaxis, systemic angioedema unrelated to the HAE episode, and sudden hypotension. Patients should be monitored closely after injection and seek immediate medical attention if any severe symptoms develop.

Icatibant is contraindicated in individuals with known hypersensitivity to icatibant or any of its excipients. Caution is also advised for patients receiving ACE inhibitors, estrogen therapy, or other bradykinin B2 antagonists, as these combinations may increase the risk of adverse reactions.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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