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 an injectable solution for subcutaneous use. It is indicated for the treatment of hereditary angioedema caused by C1‑inhibitor deficiency in patients who experience acute swelling attacks.
GNH India supplies Icatibant Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Stada Arzneimittel Ag

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Indications & Clinical Uses

Icatibant acts on the bradykinin pathway to control swelling associated with hereditary angioedema.

  • Hereditary angioedema (C1 inhibitor deficiency): reduces the severity and duration of acute swelling episodes.
  • Hereditary angioedema type I and II: provides rapid relief of symptoms by blocking bradykinin‑mediated vascular permeability.

How It Works

  • Icatibant selectively binds to the bradykinin B2 receptor, preventing bradykinin from activating the receptor. This antagonism blocks the downstream signaling that leads to vasodilation and increased vascular permeability, thereby limiting the fluid extravasation responsible for the swelling seen in hereditary angioedema attacks.

Side Effects

Icatibant may cause a range of adverse reactions, most of which are related to its subcutaneous administration and its pharmacologic action.

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 local edema.
  • Nausea: occasional gastrointestinal upset.
  • Headache: mild to moderate intensity.
  • Dizziness: transient light‑headedness.

Serious or Rare Side Effects

  • Hypersensitivity reactions: rash, pruritus, or urticaria.
  • Anaphylaxis: severe, potentially life‑threatening allergic response.
  • Severe hypotension: marked drop in blood pressure.
  • Angioedema unrelated to hereditary condition: unexpected swelling.
  • Thrombocytopenia: reduced platelet count.
  • Severe injection‑site necrosis: rare tissue damage.

Precautions & Warnings

When using Icatibant, clinicians should observe several safety measures to minimize risk.

  • Hypersensitivity monitoring: watch for signs of allergic reaction during and after injection.
  • Cardiovascular caution: use carefully in patients with unstable blood pressure or heart disease.
  • Pregnancy safety: the effect in pregnancy is unknown; avoid unless clearly needed.
  • Breastfeeding: insufficient data; consider risks versus benefits.
  • Concomitant bradykinin‑modulating drugs: assess for additive effects.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Icatibant can interact with other agents that influence the bradykinin system or cardiovascular status.

Major Interactions (Avoid)

  • ACE inhibitors: may increase bradykinin levels and exacerbate swelling.
  • Angiotensin receptor blockers (ARBs): similar risk of elevated bradykinin.
  • Neprilysin inhibitors: can raise bradykinin concentrations.

Moderate Interactions (Monitor Closely)

  • DPP‑4 inhibitors: potential additive effect on bradykinin pathways.
  • Estrogen‑containing therapies: may alter angioedema frequency.
  • Other subcutaneous biologics: monitor injection‑site reactions when administered concurrently.

Frequently Asked Questions

Icatibant Stada is used to treat acute attacks of hereditary angioedema caused by C1‑inhibitor deficiency. By blocking the bradykinin B2 receptor, it helps reduce swelling and relieve symptoms during an episode.

Icatibant works as a selective antagonist of the bradykinin B2 receptor. By binding to this receptor, it prevents bradykinin from triggering vasodilation and increased vascular permeability, which are the primary mechanisms behind 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 severity of the attack. The medication is administered subcutaneously, and the exact regimen should follow the prescriber’s instructions.

The 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 a qualified healthcare professional.

To order Icatibant Stada, submit an enquiry on the product page at gnhindia.com with 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 import documentation.

Icatibant is a bradykinin B2 receptor antagonist, whereas other treatments such as C1‑inhibitor concentrates replace the deficient protein. Icatibant provides rapid symptom relief by directly blocking bradykinin, while C1‑inhibitor products work upstream. Choice of therapy depends on clinical factors, patient preference, and physician judgment.

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 vial. If temporary temperature excursions occur, consult the product label for guidance.

Icatibant is given by subcutaneous injection, typically into the abdomen, thigh, or upper arm. The injection is performed by a trained healthcare professional or, in some cases, by the patient after proper instruction. The site should be rotated for repeated doses.

The most serious risks include severe hypersensitivity reactions such as anaphylaxis, marked hypotension, and rare cases of angioedema unrelated to hereditary angioedema. Patients should be monitored after injection for any signs of these reactions and receive appropriate medical care if they occur.

Icatibant Stada should not be used in individuals with known hypersensitivity to icatibant or any of its excipients. Caution is advised for patients receiving ACE inhibitors, ARBs, or other drugs that increase bradykinin levels, as well as for those with unstable cardiovascular conditions.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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