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 sterile solution for subcutaneous injection. It is indicated for the treatment of acute attacks of hereditary angioedema in patients with C1‑inhibitor deficiency, helping to reduce swelling and restore normal vascular function.

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

Manufacturer / TM Owner

Universal Farma, S.L.

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Indications & Clinical Uses

Icatibant is used to target the bradykinin‑mediated pathway in hereditary angioedema.

  • Hereditary angioedema (C1‑inhibitor deficiency): provides rapid reduction of swelling during acute attacks.
  • Hereditary angioedema type I: helps control edema and improve patient comfort in acute episodes.
  • Hereditary angioedema type II: facilitates faster resolution of swelling and airway protection during attacks.

How It Works

  • Icatibant selectively binds to and blocks the bradykinin B2 receptor on vascular endothelial cells. By preventing bradykinin from activating this receptor, the drug inhibits bradykinin‑induced vasodilation and increased vascular permeability, thereby reducing the fluid extravasation that causes the swelling characteristic of hereditary angioedema attacks.

Side Effects

Common Side Effects

  • Injection site pain: mild to moderate discomfort at the subcutaneous injection site.
  • Redness or swelling at injection site: transient erythema and local edema.
  • Headache or nausea: occasional mild systemic symptoms.

Serious or Rare Side Effects

  • Anaphylactic reaction: rapid onset of hives, breathing difficulty, or hypotension.
  • Paradoxical angioedema: worsening swelling despite therapy.
  • Severe hypotension: marked drop in blood pressure requiring medical attention.
  • Urticaria or widespread rash: immune‑mediated skin reactions.
  • Thrombocytopenia: rare decrease in platelet count.

Precautions & Warnings

Icatibant should be administered only under medical supervision with attention to the following precautions.

  • Dose administration: follow the prescriber's exact instructions for subcutaneous injection.
  • Renal impairment: monitor renal function and adjust use if necessary.
  • Hepatic impairment: use with caution in patients with liver disease.
  • Pregnancy: safety not established; weigh potential benefits against risks.
  • Concomitant ACE inhibitors: may increase bradykinin levels and heighten risk of angioedema.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Icatibant may interact with other agents that influence bradykinin pathways.

Major Interactions (Avoid)

  • ACE inhibitors: can elevate bradykinin levels and increase risk of angioedema.
  • Neprilysin inhibitors: may potentiate bradykinin activity, heightening adverse reactions.

Moderate Interactions (Monitor Closely)

  • Diuretics: monitor blood pressure and electrolyte balance.
  • Other antihypertensives: observe for additive hypotensive effects.
  • Hormonal contraceptives or estrogen therapy: may modestly raise bradykinin, requiring vigilance for swelling.

Frequently Asked Questions

Icatibant Universal Farma is used to treat acute attacks of hereditary angioedema (HAE) in patients who have a deficiency of C1‑inhibitor. By blocking the bradykinin B2 receptor, it helps to quickly reduce swelling and improve airway safety during an HAE episode.

Icatibant works as a selective antagonist of the bradykinin B2 receptor. By binding to this receptor, it prevents bradykinin from causing vasodilation and increased vascular permeability, which are the primary mechanisms that lead to the swelling seen in hereditary angioedema.

The dose of Icatibant Universal Farma is determined by the prescribing healthcare professional based on the patient’s clinical condition and regulatory guidelines. The prescriber will specify the exact amount, injection site, and frequency required for each acute HAE episode.

Safety of icatibant in pregnancy and lactation has not been established. Healthcare providers will weigh the potential benefits against any unknown risks before prescribing it to pregnant or nursing individuals.

To order, submit an enquiry on the product page at gnhindia.com, indicating 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 HAE therapies such as C1‑inhibitor concentrates replace the missing protein. Icatibant directly blocks the downstream mediator (bradykinin), offering rapid symptom relief without the need for plasma‑derived products.

Icatibant Universal Farma should be stored at 2‑8 °C (refrigerated). Keep the vial in its original packaging, protect it from light, and avoid freezing or shaking the solution to maintain its stability.

Icatibant is administered as a subcutaneous injection. The prescriber will instruct the patient or caregiver on the proper injection technique, site selection (typically the abdomen or thigh), and any necessary post‑injection monitoring.

Serious risks include anaphylactic reactions, paradoxical worsening of angioedema, severe hypotension, and rare immune‑mediated conditions such as thrombocytopenia. Patients should seek immediate medical attention if they experience signs of an allergic reaction or rapid swelling.

Icatibant should be avoided in individuals with known hypersensitivity to icatibant or any of its excipients. Caution is also advised for patients receiving ACE inhibitors or neprilysin inhibitors, as these combinations may increase the risk of angioedema.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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