Product image of Kayfanda (Odevixibat) supplied by GNH India

Kayfanda

Active Ingredient:
Odevixibat
Origin:
EU

Kayfanda (Odevixibat)

Odevixibat, the active ingredient in Kayfanda, is an IBAT inhibitor presented as an oral formulation for oral use. It is used to treat cholestatic liver disorders such as progressive familial intrahepatic cholestasis, Alagille syndrome, and pruritus associated with cholestatic disease in pediatric and adult patients.
GNH India supplies Kayfanda as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres and pharmacies worldwide.

Manufacturer / TM Owner

Ipsen Pharma

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Indications & Clinical Uses

Kayfanda acts on the bile acid transport pathway to manage cholestatic liver conditions.

  • Progressive familial intrahepatic cholestasis (PFIC): reduces bile acid accumulation and improves liver function.
  • Alagille syndrome: alleviates cholestasis and associated itching.
  • Pruritus associated with cholestatic liver disease: decreases bile‑acid‑induced itching and improves quality of life.

How It Works

  • Odevixibat selectively inhibits the ileal bile acid transporter (IBAT) located on the enterocytes of the distal ileum. By blocking IBAT, it reduces the enterohepatic recirculation of bile acids, leading to lower intrahepatic bile‑acid concentrations and diminished cholestatic injury. This mechanism helps control symptoms such as pruritus and supports liver function in affected patients.

Side Effects

Adverse reactions have been observed in clinical use of Odevixibat.

Common Side Effects

  • Diarrhea: frequent loose stools.
  • Abdominal pain: mild to moderate discomfort.
  • Nausea: occasional feeling of sickness.
  • Fatigue: reduced energy levels.
  • Elevated liver enzymes: mild increases in ALT/AST.
  • Vitamin deficiencies: reduced absorption of fat‑soluble vitamins.

Serious or Rare Side Effects

  • Severe dehydration: secondary to persistent diarrhea.
  • Acute liver injury: marked elevation of liver enzymes.
  • Severe abdominal pain requiring medical attention.
  • Allergic reactions: rash, urticaria, or anaphylaxis.
  • Electrolyte imbalance: especially low potassium due to gastrointestinal loss.

Precautions & Warnings

When prescribing Kayfanda, clinicians should consider several safety measures.

  • Liver function monitoring: assess ALT, AST, bilirubin regularly.
  • Hydration status: ensure adequate fluid intake to prevent dehydration.
  • Vitamin supplementation: monitor and replace fat‑soluble vitamins as needed.
  • Pregnancy and lactation: use only if the potential benefit justifies the potential risk, as safety data are limited.
  • Renal function: evaluate kidney function in patients with pre‑existing impairment.
  • Store below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Odevixibat may alter the absorption of concomitant medications.

Major Interactions (Avoid)

  • Fat‑soluble vitamin supplements: may have reduced absorption, requiring dose adjustment.
  • Oral contraceptives: decreased efficacy due to altered bile‑acid mediated absorption.
  • Lipid‑soluble drugs (e.g., cyclosporine): potential reduction in systemic exposure.

Moderate Interactions (Monitor Closely)

  • Antacids containing aluminum or magnesium: may affect gastrointestinal pH and drug dissolution.
  • Antibiotics with enterohepatic recycling (e.g., rifampin): possible decreased effectiveness.
  • Statins: monitor lipid levels as absorption may be modestly reduced.

Frequently Asked Questions

Kayfanda is indicated for progressive familial intrahepatic cholestasis (PFIC), Alagille syndrome, and pruritus associated with cholestatic liver disease. It works by reducing bile‑acid accumulation, which helps improve liver function and relieve itching in affected patients.

Odevixibat inhibits the ileal bile acid transporter (IBAT) in the distal ileum, blocking the re‑absorption of bile acids. This interruption reduces the enterohepatic circulation of bile acids, lowering their concentration in the liver and alleviating cholestasis‑related symptoms.

The dosage of Kayfanda is individualized and set by the prescribing healthcare professional based on the patient’s age, weight, disease severity, and response to therapy. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data for Odevixibat in pregnancy and lactation are limited. It should be used only if the potential benefit outweighs any possible risk to the fetus or infant, and the decision should be made by the treating physician in consultation with the patient.

To order Kayfanda, 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 and any necessary import documentation.

Kayfanda’s mechanism—IBAT inhibition—differs from other therapies such as ursodeoxycholic acid or surgical biliary diversion. By directly reducing bile‑acid re‑absorption, it offers a targeted oral option that can be used when conventional treatments are insufficient or not tolerated.

Kayfanda should be stored below 25 °C in its original packaging, protected from moisture and direct sunlight. Maintaining these conditions helps preserve the product’s stability and potency throughout its shelf life.

Kayfanda is taken orally, usually as a tablet or capsule, with or without food as directed by the prescriber. The exact administration schedule is determined by the healthcare professional based on individual patient needs.

Serious risks include severe dehydration from persistent diarrhea, acute liver injury marked by significant enzyme elevations, and rare allergic reactions such as rash or anaphylaxis. Patients should be monitored regularly for these events and seek medical attention if they occur.

Kayfanda is contraindicated in patients with known hypersensitivity to Odevixibat or any of its excipients. Caution is advised for individuals with severe hepatic impairment, uncontrolled electrolyte disturbances, or those who are pregnant or breastfeeding without a clear benefit.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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