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 solution for injection for subcutaneous use. It treats acute attacks of hereditary angioedema in patients with C1 inhibitor deficiency.

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 target bradykinin‑mediated swelling in hereditary angioedema and related conditions.

  • Acute hereditary angioedema attacks: provides rapid relief of swelling and pain.
  • Hereditary angioedema type I and II: reduces frequency and severity of episodes.
  • C1‑inhibitor deficiency‑related angioedema: controls sudden edema events.

How It Works

  • Icatibant selectively blocks the bradykinin B2 receptor, 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 attacks.

Side Effects

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

Common Side Effects

  • Injection site pain: mild to moderate discomfort at the injection site.
  • Redness or erythema: localized skin reddening.
  • Swelling at injection site: transient increase in local tissue volume.
  • Nausea: occasional gastrointestinal upset.
  • Headache: mild to moderate head pain.
  • Dizziness: transient feeling of light‑headedness.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Airway angioedema: swelling that may compromise breathing.
  • Severe hypotension: marked drop in blood pressure.
  • Thrombocytopenia: low platelet count.
  • Necrotic skin lesions: rare severe skin damage at injection site.
  • Systemic hypersensitivity: widespread rash or urticaria.

Precautions & Warnings

Before using Icatibant, consider the following safety measures.

  • Pregnancy: safety not established; use only if benefits outweigh risks.
  • Breastfeeding: caution advised as drug may pass into milk.
  • Renal impairment: monitor patients with reduced kidney function.
  • Concomitant ACE inhibitors or neprilysin inhibitors: may increase bradykinin‑related effects.
  • Known hypersensitivity: discontinue if allergic reaction occurs.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Icatibant can interact with other medications that affect bradykinin pathways or cardiovascular function.

Major Interactions (Avoid)

  • ACE inhibitors: may increase bradykinin levels and risk of angioedema.
  • Neprilysin inhibitors: additive effect on bradykinin accumulation.
  • Estrogen‑containing contraceptives: may exacerbate hereditary angioedema.

Moderate Interactions (Monitor Closely)

  • Diuretics: may alter fluid balance and affect swelling response.
  • Beta‑blockers: could mask symptoms of hypotension.
  • Other B2 receptor antagonists: potential additive pharmacologic effect.

Frequently Asked Questions

Icatibant Stada is indicated for the treatment of acute attacks of hereditary angioedema (HAE) in patients who have a deficiency of C1 inhibitor. It works by rapidly reducing swelling and associated pain during an HAE episode.

Icatibant is a selective antagonist of the bradykinin B2 receptor. By blocking this receptor, it prevents bradykinin‑induced vasodilation and increased vascular permeability, which are the primary mechanisms that cause the swelling seen in hereditary angioedema.

The dose of Icatibant Stada is determined by the prescribing clinician based on the patient’s condition, weight, and clinical response. The medication is administered as a subcutaneous injection, and the exact regimen should follow the prescriber’s instructions.

Safety of icatibant in pregnancy and lactation has not been established. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the decision should be made by the treating physician.

To place an order, 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 where required) and import documentation.

Icatibant is a bradykinin B2 receptor antagonist, whereas other HAE therapies such as C1‑inhibitor concentrates replace the deficient protein. Icatibant provides a rapid, targeted approach to block bradykinin‑mediated swelling, while C1‑inhibitor products work upstream in the complement pathway.

Icatibant Stada should be stored at 2‑8 °C (refrigerated). Keep the product in its original packaging, protect it from light, and do not freeze or shake the solution. If refrigeration is unavailable for a short period, it may be kept at controlled room temperature for up to 24 hours.

Icatibant is given as a subcutaneous injection, typically into the abdomen or thigh. The injection is performed by a healthcare professional or a trained patient, using the supplied pre‑filled syringe or autoinjector, following the prescriber’s dosing instructions.

Serious risks include anaphylaxis, airway angioedema that can compromise breathing, severe hypotension, and rare necrotic skin lesions at the injection site. Patients should be monitored for signs of allergic reaction and instructed to seek immediate medical care if severe symptoms develop.

Icatibant is contraindicated in patients with known hypersensitivity to icatibant or any of the formulation excipients. Caution is also advised for individuals taking ACE inhibitors, neprilysin inhibitors, or estrogen‑containing products, as these may increase the risk of angioedema.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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