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

Icatibant Stada

Active Ingredient:
Icatibant
Origin:
EU

Icatibant Stada (Icatibant)

Icatibant, the active ingredient in Icatibant Stada, is a bradykinin B2 receptor antagonist presented as a 30 mg/1 mL solution for injection for subcutaneous use. It treats hereditary angioedema (C1 inhibitor deficiency) in patients experiencing acute attacks.

GNH India supplies Icatibant Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Stada Arzneimittel Ag

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Indications & Clinical Uses

Icatibant is used to manage acute attacks of hereditary angioedema, a disorder driven by excessive bradykinin activity.

  • Hereditary angioedema (C1 inhibitor deficiency): reduces swelling during acute attacks.
  • Hereditary angioedema type I: provides rapid relief of edema.
  • Hereditary angioedema type II: provides rapid relief of edema.

How It Works

  • Icatibant selectively blocks the bradykinin B2 receptor, preventing bradykinin‑induced vasodilation and increased vascular permeability. By antagonizing this receptor, the drug interrupts the pathway that leads to the rapid swelling characteristic of hereditary angioedema attacks, thereby limiting edema formation.

Side Effects

Icatibant may cause a range of adverse reactions, most of which are related to the injection site or systemic exposure.

Common Side Effects

  • Injection site pain: mild to moderate discomfort at the injection site.
  • Redness or erythema: localized skin redness.
  • Swelling at injection site: transient edema.
  • Nausea: occasional gastrointestinal upset.
  • Headache: mild to moderate.
  • Dizziness: transient light‑headedness.

Serious or Rare Side Effects

  • Anaphylactic reaction: severe allergic response requiring immediate medical attention.
  • Severe hypotension: marked drop in blood pressure.
  • Angioedema unrelated to HAE: unexpected swelling of face, lips, or airway.
  • Thrombocytopenia: low platelet count observed in rare cases.
  • Necrotic injection site: tissue damage at injection site.
  • Severe hypersensitivity: rash, fever, or organ involvement.

Precautions & Warnings

Before using Icatibant, consider the following safety measures.

  • Pregnancy: safety not established; use only if potential benefit justifies the risk.
  • Breastfeeding: unknown safety; weigh benefits against possible infant exposure.
  • Renal impairment: no specific dosage adjustment, but monitor renal function.
  • Concomitant ACE inhibitors: may increase risk of bradykinin‑mediated angioedema; assess need for co‑administration.
  • Hypersensitivity: do not use in patients with known allergy to icatibant or any excipients.
  • 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 pathways or vascular tone.

Major Interactions (Avoid)

  • ACE inhibitors: may potentiate bradykinin‑mediated angioedema; avoid concurrent use.
  • Angiotensin receptor blockers: increased risk of angioedema; avoid co‑administration.
  • Prophylactic C1‑inhibitor concentrate: simultaneous use may confound clinical assessment; avoid.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may exacerbate edema; monitor for worsening symptoms.
  • Estrogen‑containing contraceptives: can increase frequency of HAE attacks; observe closely.
  • Diuretics: may affect fluid balance; watch for hypotension or electrolyte shifts.

Frequently Asked Questions

Icatibant Stada is indicated for the treatment of acute attacks of hereditary angioedema (HAE) caused by C1‑inhibitor deficiency. It helps to rapidly reduce swelling and discomfort associated with HAE episodes.

Icatibant works by selectively blocking the bradykinin B2 receptor, which stops bradykinin‑driven vasodilation and increased vascular permeability. This interruption limits the swelling that characterises hereditary angioedema attacks.

The prescribed dose of Icatibant Stada is determined by the treating physician based on the patient’s clinical condition and regulatory guidance. Dosing instructions are provided on the prescription label.

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

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 where required) and necessary import documentation.

Icatibant is a bradykinin B2 receptor antagonist, whereas other approved HAE therapies include C1‑inhibitor concentrates and kallikrein inhibitors. Icatibant is administered subcutaneously and acts directly on the bradykinin pathway, offering rapid symptom relief without the need for intravenous infusion.

Icatibant Stada should be stored at 2‑8 °C (refrigerated). Keep the vial in its original packaging, protect it from light, and do not freeze or shake the solution before use.

Icatibant Stada is supplied as a 30 mg/1 mL solution for subcutaneous injection. The injection is given into the abdominal wall or thigh, following aseptic technique as instructed by the prescribing clinician.

The most serious risks include anaphylaxis, severe hypotension, and unexpected angioedema unrelated to hereditary angioedema. Patients should be monitored for signs of allergic reaction and instructed to seek immediate medical attention if severe symptoms develop.

Icatibant Stada is contraindicated in individuals with known hypersensitivity to icatibant or any of its excipients. Caution is also advised for patients with uncontrolled cardiovascular disease or those receiving ACE inhibitors without appropriate medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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