Product image of Icatibanto Stada (Icatibant) supplied by GNH India

Icatibanto Stada

Active Ingredient:
Icatibant
Origin:
EU

Icatibanto Stada (Icatibant)

Icatibant, the active ingredient in Icatibanto Stada, is a bradykinin B2 receptor antagonist presented as a sterile solution for subcutaneous use. It is indicated for the treatment of hereditary angioedema in patients with C1‑inhibitor deficiency, providing rapid relief of swelling episodes and is currently manufactured under strict EU quality standards.

GNH India supplies Icatibanto Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with established logistics for temperature‑controlled shipment and regulatory support across multiple regions.

Manufacturer / TM Owner

Laboratorio Stada, S.L.

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Indications & Clinical Uses

  • Icatibant is used to target bradykinin‑mediated pathways in hereditary angioedema, reducing swelling and associated symptoms.
  • Hereditary angioedema (C1‑inhibitor deficiency): provides rapid relief of acute swelling episodes.
  • Hereditary angioedema attacks (laryngeal, abdominal, peripheral): reduces airway obstruction risk and abdominal pain.
  • Hereditary angioedema prophylaxis: decreases frequency of recurrent attacks.

How It Works

  • Icatibant selectively blocks the bradykinin B2 receptor on vascular endothelial cells, preventing bradykinin from inducing vasodilation and increased vascular permeability. By inhibiting this receptor, the drug curtails the cascade that leads to fluid extravasation and edema, thereby mitigating the acute swelling characteristic of hereditary angioedema.

Side Effects

Common Side Effects

  • Injection site pain or erythema.
  • Local swelling or induration.
  • Nausea or mild gastrointestinal discomfort.
  • Headache.
  • Dizziness.
  • Transient fatigue.

Serious or Rare Side Effects

  • Anaphylactic or severe hypersensitivity reactions.
  • Angioedema unrelated to hereditary episodes.
  • Severe hypotension.
  • Thrombocytopenia.
  • Infections at the injection site.
  • Cardiovascular events such as myocardial infarction (very rare).

Precautions & Warnings

Before initiating therapy, consider patient history and monitor for adverse reactions.

  • Hypersensitivity assessment: evaluate for known allergy to icatibant or excipients.
  • Anaphylaxis vigilance: observe for signs of severe allergic response after injection.
  • Pregnancy and lactation: safety not established; use only if benefit outweighs risk.
  • Renal or hepatic impairment: no specific dose adjustment, but monitor clinical response.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Icatibant may interact with drugs that influence bradykinin levels or cardiovascular function.

Major Interactions (Avoid)

  • ACE inhibitors: can increase bradykinin and heighten risk of angioedema.
  • Neprilysin inhibitors: elevate bradykinin concentrations, potentially reducing icatibant efficacy.
  • Other bradykinin‑enhancing agents: may exacerbate swelling.

Moderate Interactions (Monitor Closely)

  • Estrogen‑containing contraceptives: may modestly increase angioedema risk.
  • NSAIDs: can aggravate hypersensitivity reactions.
  • Diuretics: monitor blood pressure due to possible additive hypotensive effect.

Frequently Asked Questions

Icatibanto Stada contains icatibant, which is prescribed to treat hereditary angioedema caused by C1‑inhibitor deficiency. It works by rapidly reducing swelling during acute attacks and can also be used to lessen the frequency of recurrent episodes in affected patients.

Icatibant is a selective antagonist of the bradykinin B2 receptor. By blocking this receptor on blood vessels, it stops bradykinin‑induced vasodilation and increased permeability, thereby preventing the fluid leakage that causes the swelling characteristic of hereditary angioedema.

The dosage and administration schedule for Icatibanto Stada are determined by the prescribing healthcare professional based on the patient’s clinical condition, severity of attacks, and individual response. The prescriber will provide specific instructions for each case.

Safety data for icatibant in pregnancy and lactation are limited, and the product is classified as having an unknown pregnancy category. It should only be used if the potential benefit justifies any possible risk to the fetus or infant, and under close medical supervision.

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.

Icatibanto Stada is a bradykinin B2 receptor antagonist, whereas alternative therapies may include C1‑esterase inhibitor concentrates or newer monoclonal antibodies targeting kallikrein. Icatibant offers rapid subcutaneous administration and direct blockade of bradykinin, making it effective for acute attacks, while other options may focus on replacement or upstream inhibition.

The product must be stored at 2‑8 °C (refrigerated). Keep it in the original packaging, protect it from light, and avoid freezing or shaking the vial, as temperature stability is essential for maintaining potency.

Icatibanto Stada is supplied as a sterile solution for subcutaneous injection. The prescriber or a trained healthcare professional will administer the dose into the subcutaneous tissue, typically in the abdomen or thigh, following aseptic technique.

The most serious risks include severe hypersensitivity reactions such as anaphylaxis, unexpected angioedema unrelated to hereditary episodes, and significant hypotension. Patients should be observed after injection and instructed to seek immediate medical attention if they experience any signs of a severe reaction.

Patients with a known hypersensitivity to icatibant or any of its excipients should avoid the product. Additionally, individuals currently receiving ACE inhibitors or other bradykinin‑enhancing drugs should discuss alternative therapies with their physician due to increased risk of angioedema.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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