Product image of Icatibant Medical Valley (Icatibant) supplied by GNH India

Icatibant Medical Valley

Active Ingredient:
Icatibant
Origin:
EU

Icatibant Medical Valley (Icatibant)

Icatibant, the active ingredient in Icatibant Medical Valley, is a bradykinin B2 receptor antagonist presented as a subcutaneous solution for subcutaneous use. It treats acute attacks of hereditary angioedema in patients with confirmed HAE.
GNH India supplies Icatibant Medical Valley as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Medical Valley Invest Ab

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Indications & Clinical Uses

Icatibant acts on the bradykinin pathway to relieve swelling in hereditary angioedema.

  • Hereditary angioedema (HAE) acute attacks: rapidly reduces edema and associated pain by blocking bradykinin‑mediated vascular permeability.

How It Works

  • Icatibant is a selective competitive antagonist of the bradykinin B2 receptor. By binding to this receptor, it prevents bradykinin from inducing vasodilation and increasing vascular permeability, thereby limiting the swelling and pain characteristic of hereditary angioedema attacks.

Side Effects

Icatibant may cause a range of adverse reactions following subcutaneous administration.

Common Side Effects

  • Injection site pain: mild to moderate discomfort at the injection site.
  • Redness or swelling at injection site: localized erythema or edema.
  • Nausea: occasional feeling of queasiness.
  • Headache: transient mild headache.
  • Dizziness: brief episodes of light‑headedness.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Angioedema of the face or airway: worsening swelling that could compromise breathing.
  • Hypotension: sudden drop in blood pressure.
  • Thrombocytopenia: low platelet count observed in rare cases.

Precautions & Warnings

Before using Icatibant, consider the following safety measures.

  • Hypersensitivity: avoid if the patient has known allergy to icatibant or any excipients.
  • Pregnancy: use only if the potential benefit justifies the potential risk to the fetus.
  • Breastfeeding: weigh benefits against possible effects on the infant.
  • Concomitant bradykinin‑modulating drugs: monitor for additive effects on blood pressure.
  • Renal or hepatic impairment: adjust monitoring as needed.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Icatibant may interact with other medicines, requiring attention to the level of risk.

Major Interactions (Avoid)

  • ACE inhibitors: combined use may increase risk of angioedema.
  • Angiotensin receptor blockers (ARBs): may potentiate bradykinin‑related swelling.

Moderate Interactions (Monitor Closely)

  • Estrogen‑containing oral contraceptives: may affect HAE severity.
  • Other subcutaneous biologics: monitor injection site reactions.
  • Diuretics: observe for blood pressure changes.
  • NSAIDs: watch for additive edema risk.

Frequently Asked Questions

Icatibant Medical Valley is indicated for the treatment of acute attacks of hereditary angioedema (HAE). It works by rapidly reducing swelling and pain associated with HAE episodes, providing relief when administered promptly during an attack.

Icatibant is a selective competitive antagonist of the bradykinin B2 receptor. By blocking this receptor, it prevents bradykinin from causing vasodilation and increased vascular permeability, which are the primary mechanisms behind the swelling seen in hereditary angioedema.

The dose of icatibant is determined by the prescribing clinician based on the patient’s condition and clinical guidelines. Typically, a single subcutaneous injection is given at the onset of an HAE attack, with additional doses administered only if medically indicated.

Safety data for icatibant in pregnancy and lactation are limited. It should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision should be made in consultation with a 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 if needed) and required import documentation.

The primary alternative for HAE is C1‑esterase inhibitor replacement therapy, which restores deficient protein function. Icatibant, by contrast, blocks the bradykinin B2 receptor directly, offering a rapid, receptor‑targeted approach. Choice of therapy depends on patient preference, attack severity, and clinical response.

Icatibant should be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. If refrigeration is temporarily unavailable, the product may be kept at controlled room temperature for a limited period as specified in the product label.

Icatibant is administered as a subcutaneous injection, usually into the abdomen or thigh. The injection site should be cleaned with an alcohol swab, and the medication delivered using the pre‑filled syringe provided, following aseptic technique and the prescriber’s instructions.

The most serious adverse reactions include anaphylaxis, severe angioedema affecting the airway, and hypotension. Patients should be monitored closely after injection, and any signs of respiratory distress, swelling of the face or throat, or sudden drop in blood pressure require immediate medical attention.

Icatibant is contraindicated in individuals with a known hypersensitivity to icatibant or any of its excipients. Caution is also advised for patients who have experienced severe allergic reactions to other bradykinin‑targeting agents.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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