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

Icatibant Viatris

Active Ingredient:
Icatibant
Origin:
EU

Icatibant Viatris (Icatibant)

Icatibant, the active ingredient in Icatibant Viatris, is a Bradykinin B2 receptor antagonist presented as a subcutaneous formulation for subcutaneous use. It is indicated for the treatment of acute attacks of hereditary angioedema in patients with confirmed diagnosis. GNH India supplies Icatibant Viatris as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Mylan Germany Gmbh

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Indications & Clinical Uses

Icatibant is a targeted therapy for hereditary angioedema that works by blocking the bradykinin B2 receptor pathway.

  • Acute hereditary angioedema attacks: reduces swelling and pain by inhibiting bradykinin‑mediated vascular permeability.
  • Hereditary angioedema type I: provides rapid symptom relief during episodes.
  • Hereditary angioedema type II: helps control acute swelling events.

How It Works

  • Icatibant acts as a competitive antagonist at the bradykinin B2 receptor, preventing bradykinin from binding and activating the receptor. This inhibition blocks bradykinin‑induced vasodilation and increased vascular permeability, thereby reducing the swelling associated with hereditary angioedema attacks.

Side Effects

Icatibant may cause a range of adverse reactions, most of which are mild to moderate in severity.

Common Side Effects

  • Injection site pain: discomfort at the site of subcutaneous administration.
  • Redness or swelling at injection site: localized inflammatory response.
  • Nausea: mild gastrointestinal upset.
  • Headache: transient cranial discomfort.
  • Dizziness: occasional light‑headedness.

Serious or Rare Side Effects

  • Hypersensitivity reactions: rash, urticaria, or anaphylaxis.
  • Severe injection site necrosis: tissue damage requiring medical attention.
  • Thrombocytopenia: low platelet count observed in rare cases.
  • Acute hypotension: sudden drop in blood pressure.
  • Severe abdominal pain: may indicate internal complications.

Precautions & Warnings

Before using Icatibant, consider the following safety measures.

  • Assess patient history: verify diagnosis of hereditary angioedema and prior response to therapy.
  • Monitor for hypersensitivity: observe for signs of allergic reaction after injection.
  • Evaluate concomitant medications: consider potential additive effects on blood pressure.
  • Use in pregnancy and lactation: only if clearly needed, after risk‑benefit assessment by the prescriber.
  • Renal or hepatic impairment: adjust monitoring as appropriate.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Icatibant may interact with other medications; awareness of these interactions helps ensure safe use.

Major Interactions (Avoid)

  • ACE inhibitors: may increase bradykinin levels, potentially reducing Icatibant efficacy.
  • Angiotensin receptor blockers (ARBs): similar risk of elevated bradykinin.

Moderate Interactions (Monitor Closely)

  • Diuretics: may affect blood pressure response.
  • Other B2 receptor antagonists: additive pharmacologic effects.
  • Antihistamines: monitor for overlapping adverse reactions.

Frequently Asked Questions

Icatibant Viatris is used to treat acute attacks of hereditary angioedema (HAE) in patients with confirmed type I or type II disease. By blocking the bradykinin B2 receptor, it helps reduce swelling and associated symptoms during an HAE episode.

Icatibant is a competitive antagonist of the bradykinin B2 receptor. It prevents bradykinin from binding to this receptor, thereby inhibiting the cascade that leads to vasodilation and increased vascular permeability, which are responsible for the swelling seen in HAE attacks.

The specific dose and administration schedule are determined by the prescribing healthcare professional based on the patient’s condition, severity of the attack, and clinical guidelines. Patients should follow the prescriber’s instructions precisely.

Safety data for Icatibant in pregnancy and lactation are limited. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made by the treating physician after a thorough risk‑benefit assessment.

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 logistics if needed) and necessary import documentation.

Icatibant is a bradykinin B2 receptor antagonist, whereas other options such as C1‑esterase inhibitor concentrates act by replacing deficient plasma proteins. Icatibant offers rapid subcutaneous administration and targets the downstream mediator bradykinin directly, providing an alternative mechanism of action.

Icatibant 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 by subcutaneous injection, typically into the abdomen or thigh. The injection is performed by a trained healthcare professional or, after proper instruction, by the patient or caregiver at the onset of an HAE attack.

Serious risks include hypersensitivity reactions such as rash, urticaria, or anaphylaxis, as well as rare events like severe injection‑site necrosis, thrombocytopenia, and acute hypotension. Patients should be monitored for these signs and seek immediate medical attention if they occur.

Icatibant is contraindicated in patients with known hypersensitivity to the drug or any of its excipients. Caution is also advised for individuals with severe cardiovascular disease, uncontrolled hypertension, or those taking ACE inhibitors or ARBs without appropriate medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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