Product image of Kadderum (Eltrombopag) supplied by GNH India

Kadderum

Active Ingredient:
Eltrombopag
Origin:
EU

Kadderum (Eltrombopag)

Eltrombopag, the active ingredient in Kadderum, is a thrombopoietin receptor agonist presented as an oral tablet for oral use. It is indicated for chronic immune thrombocytopenia, severe aplastic anemia, and hepatitis C‑associated thrombocytopenia in appropriate patients.

GNH India supplies Kadderum as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide, providing reliable, quality‑assured medication across multiple therapeutic areas. The company adheres to stringent regulatory standards and offers comprehensive logistics support for global distribution.

Manufacturer / TM Owner

Genepharm S.A.

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Indications & Clinical Uses

Eltrombopag is used to treat disorders characterized by low platelet production.

  • Chronic immune thrombocytopenia (ITP): Increases platelet counts to reduce bleeding risk.
  • Severe aplastic anemia: Stimulates platelet production as part of supportive therapy.
  • Hepatitis C‑associated thrombocytopenia: Improves platelet levels in patients with liver disease.

How It Works

  • Eltrombopag binds to the thrombopoietin receptor (c‑Mpl) on megakaryocyte precursors, mimicking endogenous thrombopoietin. This triggers JAK‑STAT signaling, promoting proliferation and differentiation of megakaryocytes and thereby enhancing platelet production without relying on natural hormone levels.

Side Effects

Eltrombopag may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Nausea
  • Diarrhea
  • Fatigue
  • Elevated liver enzymes

Serious or Rare Side Effects

  • Hepatotoxicity
  • Thromboembolic events
  • Severe skin reactions such as Stevens‑Johnson syndrome

Precautions & Warnings

When prescribing Eltrombopag, clinicians should consider several precautionary measures to ensure patient safety.

  • Baseline liver function: Assess hepatic enzymes before initiating therapy.
  • Monitor platelet counts: Adjust dose based on regular platelet monitoring.
  • Cardiovascular risk: Evaluate for history of thromboembolic disease.
  • Concomitant medications: Review for potential interactions affecting metabolism.
  • Pregnancy and lactation: Use only if potential benefit justifies potential risk; data limited.
  • Store at ambient temperature: Keep below 25 °C in original packaging, protect from moisture.

Avoid Interactions

Eltrombopag can interact with other medicines, influencing its efficacy or safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): May markedly reduce drug exposure.
  • Antacids containing polyvalent cations (e.g., aluminum, magnesium): Can impair absorption if taken simultaneously.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inhibitors (e.g., fluconazole, erythromycin): May increase plasma levels.
  • Warfarin: May enhance anticoagulant effect; monitor INR.
  • Live vaccines: Potentially reduced efficacy; assess risk/benefit.

Frequently Asked Questions

Kadderum contains eltrombopag, a thrombopoietin receptor agonist prescribed to increase platelet production in conditions such as chronic immune thrombocytopenia, severe aplastic anemia, and hepatitis C‑associated thrombocytopenia.

Eltrombopag activates the thrombopoietin receptor (c‑Mpl) on megakaryocyte precursors, initiating intracellular signaling that drives megakaryocyte proliferation and differentiation, ultimately raising platelet counts in the bloodstream.

The dosage of Kadderum is individualized; a qualified prescriber determines the appropriate strength and schedule based on the patient’s condition, laboratory values, and response to therapy.

Safety data for eltrombopag 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 must be made by the treating physician.

To order Kadderum, 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 and any necessary import documentation.

The primary alternative is romiplostim, another thrombopoietin receptor agonist administered by injection. Kadderum offers an oral formulation, which may be preferred for convenience, whereas romiplostim requires subcutaneous dosing. Both aim to raise platelet counts, but their pharmacokinetics and administration routes differ.

Kadderum tablets should be stored at ambient temperature, preferably below 25 °C, in the original container to protect them from moisture and light. Keep out of reach of children and do not use after the expiry date.

Kadderum is taken orally with a glass of water, usually on an empty stomach to improve absorption. The tablet should be swallowed whole; it should not be crushed, chewed, or split unless specifically instructed by a healthcare professional.

Serious risks include hepatotoxicity, thromboembolic events such as deep‑vein thrombosis or pulmonary embolism, and severe skin reactions like Stevens‑Johnson syndrome. Patients should be monitored regularly for liver function abnormalities and signs of abnormal clotting.

Kadderum is contraindicated in patients with known hypersensitivity to eltrombopag or any tablet excipients, and it should be avoided in individuals with active uncontrolled thrombotic disorders. Caution is also advised for patients with severe liver impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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