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 injection for subcutaneous use. It treats hereditary angioedema attacks in adults.

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 is a targeted therapy for hereditary angioedema, acting on the bradykinin pathway.

  • Hereditary angioedema (HAE) attacks: provides rapid relief of swelling episodes in adult patients.

How It Works

  • Icatibant selectively and competitively blocks the bradykinin B2 receptor, preventing bradykinin from binding and activating the receptor. This inhibition reduces bradykinin‑mediated vasodilation and vascular permeability, thereby limiting the fluid extravasation that causes swelling during hereditary angioedema attacks.

Side Effects

Adverse reactions may occur following subcutaneous administration of icatibant.

Common Side Effects

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

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Worsening angioedema: paradoxical increase in swelling.
  • Severe hypotension: marked drop in blood pressure.
  • Urticaria: widespread hives.
  • Thrombocytopenia: low platelet count observed in rare cases.

Precautions & Warnings

Prior to administration, clinicians should evaluate patient history and monitor for potential adverse events.

  • Assess severity of HAE attack: confirm that the episode warrants icatibant therapy.
  • Monitor for hypersensitivity: watch for signs of allergic reaction during and after injection.
  • Avoid in known hypersensitivity: do not use in patients with documented icatibant allergy.
  • Use cautiously in cardiovascular disease: monitor blood pressure and heart rate.
  • Concomitant ACE inhibitor use: consider increased bradykinin risk.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Icatibant may interact with other medications that influence bradykinin levels or vascular tone.

Major Interactions (Avoid)

  • ACE inhibitors: may increase bradykinin and heighten risk of angioedema.
  • Neprilysin inhibitors: can elevate bradykinin concentrations, potentially reducing icatibant efficacy.

Moderate Interactions (Monitor Closely)

  • Other B2 receptor antagonists: concurrent use may lead to additive effects.
  • Corticosteroids: may mask early signs of hypersensitivity.
  • Antihistamines: monitor for altered response to allergic reactions.

Frequently Asked Questions

Icatibant Medical Valley is used to treat acute attacks of hereditary angioedema (HAE) in adult patients. It works by rapidly reducing swelling associated with HAE episodes, providing relief from the potentially life‑threatening symptoms of the condition.

Icatibant is a selective competitive 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 swelling during hereditary angioedema attacks.

The dose of icatibant is determined by the prescribing healthcare professional based on the patient’s clinical condition and regulatory guidelines. The prescriber will decide the appropriate amount and frequency for each individual case.

Safety data for icatibant in pregnancy and lactation are limited. Healthcare providers should weigh the potential benefits against any possible risks before prescribing it to pregnant or breastfeeding women, and use it only if clearly indicated.

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, and will request trade or institutional credentials before providing pricing, availability, shipping details (including cold‑chain handling if needed) and import documentation.

Icatibant is a bradykinin B2 receptor antagonist, whereas other acute HAE therapies, such as C1‑esterase inhibitor concentrates, replace a deficient protein. Icatibant directly blocks the downstream effects of bradykinin, offering a rapid, targeted approach that does not require plasma‑derived products.

Icatibant should be stored at 2‑8 °C in a refrigerator, 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 by subcutaneous injection, typically into the abdomen or thigh. The injection is performed by a trained healthcare professional or, in some cases, by the patient after proper instruction.

The most serious risks include anaphylaxis, severe hypotension, and paradoxical worsening of angioedema. Patients should be monitored closely after injection for any signs of these reactions, and emergency medical care should be sought immediately if they occur.

Icatibant should not be used in individuals with known hypersensitivity to the drug or any of its excipients. Caution is also advised for patients with severe cardiovascular disease or those taking ACE inhibitors, as the risk of adverse reactions may be increased.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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