Product image of Icatibant Fresenius (Icatibant Acetate) supplied by GNH India

Icatibant Fresenius

Active Ingredient:
Icatibant Acetate
Origin:
EU

Icatibant Fresenius (Icatibant Acetate)

Icatibant acetate, the active ingredient in Icatibant Fresenius, is a bradykinin B2 receptor antagonist presented as a sterile solution for injection for subcutaneous administration. It is indicated for the treatment of acute attacks of hereditary angioedema (HAE) types I and II in patients with a confirmed diagnosis, providing rapid symptom relief.

GNH India supplies Icatibant Fresenius as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring quality‑controlled distribution across EU and other regulated markets and research institutions.

Manufacturer / TM Owner

Fresenius Kabi Polska Sp. Z O.O.

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Indications & Clinical Uses

Icatibant Fresenius is used to treat bradykinin‑mediated hereditary angioedema attacks.

  • Acute hereditary angioedema type I: rapid reduction of swelling during an attack.
  • Acute hereditary angioedema type II: rapid reduction of swelling during an attack.
  • Hereditary angioedema attacks (any type): alleviation of symptoms and restoration of normal function.

How It Works

  • Icatibant acetate selectively blocks the bradykinin B2 receptor on vascular endothelial cells, preventing bradykinin from binding and triggering vasodilation and increased vascular permeability. By inhibiting this pathway, the drug reduces the fluid extravasation that causes the characteristic swelling of hereditary angioedema, leading to faster resolution of attacks.

Side Effects

Icatibant Fresenius may cause a range of adverse reactions.

Common Side Effects

  • Injection site pain or erythema.
  • Local swelling or induration at the injection site.
  • Headache.
  • Nausea.
  • Dizziness.
  • Fatigue.

Serious or Rare Side Effects

  • Hypersensitivity reactions, including rash or urticaria.
  • Anaphylaxis or severe systemic allergic response.
  • Severe hypotension.
  • Angioedema unrelated to HAE.
  • Infection at the injection site.

Precautions & Warnings

Before using Icatibant Fresenius, consider the following safety measures.

  • Confirm diagnosis: ensure the patient has a documented hereditary angioedema type I or II.
  • Monitor for hypersensitivity: observe the patient after injection for any allergic signs.
  • Avoid in patients with known hypersensitivity to icatibant acetate or any excipients.
  • Use with caution in patients receiving ACE inhibitors, as bradykinin levels may be elevated.
  • Pregnancy and lactation: limited data are available; weigh potential benefits against unknown risks.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Icatibant Fresenius can interact with other medicines that affect the bradykinin pathway or vascular tone.

Major Interactions (Avoid)

  • ACE inhibitors: may increase bradykinin levels and raise the risk of angioedema.
  • C1‑esterase inhibitor concentrates: concurrent use is not recommended due to overlapping mechanisms.

Moderate Interactions (Monitor Closely)

  • Angiotensin receptor blockers: may modestly increase bradykinin activity.
  • Estrogen‑containing oral contraceptives: can influence HAE severity and may require closer monitoring.
  • Other bradykinin‑targeting agents: combined use could alter efficacy or safety profile.

Frequently Asked Questions

Icatibant Fresenius is a prescription injectable medication used to treat acute attacks of hereditary angioedema (HAE) types I and II. It works by rapidly reducing the swelling and pain associated with these bradykinin‑mediated episodes.

Icatibant acetate is a selective antagonist of the bradykinin B2 receptor. By blocking this receptor on blood‑vessel walls, it prevents bradykinin‑induced vasodilation and increased vascular permeability, which are the primary drivers of swelling in hereditary angioedema.

The dosage and administration schedule for Icatibant Fresenius are determined by the prescribing healthcare professional based on the patient’s clinical condition, severity of the attack, and regulatory guidelines. The prescriber will specify the exact dose and timing.

Safety data for icatibant acetate in pregnancy and lactation are limited. Healthcare providers should evaluate the potential benefits against possible risks before prescribing it to pregnant or nursing women, and use it only if clearly needed.

To order Icatibant Fresenius, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if required) and import documentation.

Icatibant Fresenius is a bradykinin B2 receptor antagonist, whereas other approved HAE therapies include C1‑esterase inhibitor concentrates and kallikrein inhibitors. Icatibant acts directly on the bradykinin pathway, offering rapid symptom relief after subcutaneous injection, while the alternatives work upstream or replace deficient proteins.

Icatibant Fresenius 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 solution, as these conditions can affect its stability and efficacy.

The medication is supplied as a sterile solution for injection and is administered subcutaneously, typically into the abdomen or thigh. The injection is performed by a trained healthcare professional or, in some cases, by the patient after appropriate instruction.

Serious risks include hypersensitivity reactions such as anaphylaxis, severe hypotension, and rare cases of systemic angioedema unrelated to HAE. Patients should be observed after injection and instructed to seek immediate medical attention if they experience any signs of a severe allergic reaction.

Icatibant Fresenius should not be used by individuals with a known hypersensitivity to icatibant acetate or any of its excipients. Caution is also advised for patients receiving ACE inhibitors or other agents that increase bradykinin levels, and it is generally avoided in unconfirmed diagnoses of HAE.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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