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

Icatibant Sandoz

Active Ingredient:
Icatibant
Origin:
EU

Icatibant Sandoz (Icatibant)

Icatibant, the active ingredient in Icatibant Sandoz, is a bradykinin B2 receptor antagonist presented as an injection solution for subcutaneous use. It treats acute attacks of hereditary angioedema in patients with C1‑inhibitor deficiency.

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

Manufacturer / TM Owner

Sandoz A/S

1
Pack/s
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Indications & Clinical Uses

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

  • Acute hereditary angioedema (C1‑inhibitor deficiency): rapidly reduces swelling during attacks.
  • Hereditary angioedema type I: provides quick symptom relief and improves airway safety.
  • Hereditary angioedema type II: alleviates abdominal pain and facial swelling associated with attacks.

How It Works

  • Icatibant selectively blocks the bradykinin B2 receptor on vascular endothelial cells, preventing bradykinin‑induced vasodilation and increased vascular permeability. By inhibiting this pathway, it curtails the fluid extravasation that causes the swelling characteristic 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 exposure.

Common Side Effects

  • Injection site pain: discomfort at the site of subcutaneous administration.
  • Injection site erythema: redness around the injection area.
  • Nausea: feeling of sickness or urge to vomit.
  • Headache: mild to moderate head pain.
  • Dizziness: sensation of light‑headedness.
  • Flushing: transient redness of the skin.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Severe hypotension: marked drop in blood pressure.
  • Angioedema: swelling of deeper skin layers, potentially affecting the airway.
  • Urticaria: hives or itchy welts.
  • Severe injection site reactions: necrosis or extensive swelling.
  • Thrombocytopenia: low platelet count observed rarely.

Precautions & Warnings

Before prescribing Icatibant, clinicians should consider several safety measures.

  • Confirm diagnosis: ensure the patient has hereditary angioedema with C1‑inhibitor deficiency.
  • Monitor hypersensitivity: watch for signs of anaphylaxis or severe allergic reactions.
  • Contraindication check: avoid use in patients with known hypersensitivity to icatibant or its excipients.
  • Pregnancy and lactation: use only if the potential benefit justifies the potential risk, as safety data are limited.
  • Injection technique: do not administer multiple injections at the same site to reduce local tissue damage.
  • 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 affect injection site tolerance.

Major Interactions (Avoid)

  • ACE inhibitors: may increase bradykinin levels and raise the risk of angioedema.
  • Estrogen‑containing contraceptives: can exacerbate hereditary angioedema symptoms.
  • Other bradykinin B2 antagonists: additive pharmacologic effect may increase adverse events.

Moderate Interactions (Monitor Closely)

  • C1‑inhibitor concentrate: concurrent use may complicate assessment of therapeutic response.
  • NSAIDs: may heighten the likelihood of local injection site reactions.

Frequently Asked Questions

Icatibant Sandoz is indicated for the treatment of acute attacks of hereditary angioedema in patients with C1‑inhibitor deficiency. It works by rapidly reducing swelling and improving airway safety during an attack.

Icatibant selectively blocks the bradykinin B2 receptor on blood vessel walls, preventing bradykinin‑induced vasodilation and increased permeability. This inhibition stops the fluid leakage that causes the swelling seen in hereditary angioedema.

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

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 supplies 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.

Icatibant is a bradykinin B2 receptor antagonist, whereas other options such as C1‑inhibitor concentrates replace the deficient protein. Icatibant acts directly on the bradykinin pathway, providing rapid symptom relief without requiring plasma‑derived products.

Icatibant Sandoz should be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. Keep the product in its original packaging until use to maintain stability.

Icatibant is given as a subcutaneous injection, typically into the abdomen or thigh. The injection is performed by a trained healthcare professional or, after appropriate instruction, by the patient or caregiver.

The most serious risks include severe allergic reactions such as anaphylaxis, marked hypotension, and rare cases of angioedema that may affect the airway. Patients should be monitored closely after administration for any signs of these events.

Icatibant should not be used in individuals with known hypersensitivity to icatibant or any of its excipients. Caution is also advised for patients with uncontrolled cardiovascular disease or those who are pregnant or breastfeeding unless clearly indicated by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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