Product image of Mylatabi (Eltrombopag) supplied by GNH India

Mylatabi

Active Ingredient:
Eltrombopag
Origin:
EU

Mylatabi (Eltrombopag)

Eltrombopag, the active ingredient in Mylatabi, is a thrombopoietin receptor agonist presented as an oral dosage form for oral use. It stimulates platelet production and is indicated for conditions such as immune thrombocytopenia, hepatitis C‑associated thrombocytopenia, and severe aplastic anemia in appropriate patients.

GNH India supplies Mylatabi as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide, with established quality‑assured distribution networks and regulatory compliance across EU and other markets.

Manufacturer / TM Owner

Tillomed Malta Ltd

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Indications & Clinical Uses

Eltrombopag is used to treat hematologic disorders characterized by low platelet counts.

  • Immune thrombocytopenia (ITP): Increases platelet counts to reduce bleeding risk in patients with chronic ITP.
  • Hepatitis C‑associated thrombocytopenia: Improves platelet production in patients with thrombocytopenia secondary to chronic hepatitis C infection.
  • Severe aplastic anemia: Enhances platelet generation as part of therapy for patients with severe aplastic anemia.

How It Works

  • Eltrombopag binds to the transmembrane domain of the thrombopoietin (TPO) receptor (c‑Mpl) on megakaryocyte progenitor cells, mimicking endogenous TPO. This activation triggers intracellular signaling pathways, notably JAK/STAT and MAPK, leading to proliferation and differentiation of megakaryocytes and increased platelet production. The drug’s oral bioavailability allows systemic exposure sufficient to sustain platelet counts in affected patients and contributes to improved hemostasis.

Side Effects

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

Common Side Effects

  • Nausea: mild to moderate gastrointestinal discomfort.
  • Diarrhea: loose stools that may be self‑limiting.
  • Fatigue: generalized tiredness.
  • Elevated liver enzymes: transient increases in ALT/AST.
  • Headache: mild cranial pain.

Serious or Rare Side Effects

  • Hepatotoxicity: significant liver injury requiring monitoring.
  • Thromboembolic events: arterial or venous clot formation.
  • Severe skin reactions: such as Stevens‑Johnson syndrome.
  • Bone marrow fibrosis: rare progression of marrow scarring.
  • Myelosuppression: unexpected drop in other blood cell lines.

Precautions & Warnings

When prescribing Eltrombopag, clinicians should consider several precautionary measures to ensure safe use.

  • Baseline liver function: assess ALT/AST before initiating therapy.
  • Monitor platelet counts: adjust dose based on weekly platelet monitoring.
  • Concomitant anticoagulants: evaluate bleeding risk when used with anticoagulant drugs.
  • Pregnancy and lactation: avoid use unless benefits outweigh potential risks.
  • Drug interactions: review patient’s medication list for known major interactions.
  • Store at ambient temperature: keep below 25°C in original packaging, protect from moisture.

Avoid Interactions

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

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): may markedly reduce drug exposure.
  • Antacids containing polyvalent cations: decrease oral absorption if taken simultaneously.

Moderate Interactions (Monitor Closely)

  • Immunosuppressants (e.g., cyclosporine, tacrolimus): may increase plasma levels.
  • Warfarin: potential alteration of INR, requiring closer monitoring.
  • Oral contraceptives: possible reduced effectiveness, advise alternative contraception.

Frequently Asked Questions

Mylatabi contains eltrombopag and is prescribed to increase platelet counts in patients with immune thrombocytopenia, hepatitis C‑associated thrombocytopenia, and severe aplastic anemia. By raising platelet levels, it helps reduce bleeding risk and supports hematologic recovery in these conditions.

Eltrombopag mimics the natural hormone thrombopoietin by binding to the c‑Mpl receptor on megakaryocyte precursors. This activates intracellular JAK/STAT and MAPK pathways, stimulating the proliferation and maturation of megakaryocytes, which in turn boosts platelet production.

The dosage of Mylatabi is individualized. A qualified prescriber determines the appropriate starting dose and any adjustments based on the patient’s platelet response, liver function, and overall clinical condition. No fixed regimen is provided here.

Safety data for eltrombopag in pregnancy and lactation are limited. It should only be used when the potential benefit justifies any possible risk to the fetus or infant, and the decision must be made by the treating physician.

To request Mylatabi, 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 main alternative is romiplostim, an injectable TPO receptor agonist. While both increase platelet production, eltrombopag is taken orally, offering convenience, whereas romiplostim requires subcutaneous administration. Choice depends on patient preference, clinical response, and specific safety considerations.

Mylatabi tablets should be stored at ambient temperature, preferably below 25 °C. Keep them in the original container, protect from moisture and direct sunlight, and ensure they are out of reach of children.

Mylatabi is taken orally, usually with a glass of water. It can be taken with or without food, but patients should follow the prescriber’s instructions regarding timing relative to meals to optimize absorption.

Serious adverse events include hepatotoxicity, thromboembolic complications, severe skin reactions such as Stevens‑Johnson syndrome, and rare bone‑marrow fibrosis. Patients should be monitored regularly for liver function, clotting signs, and any unusual skin changes.

Mylatabi is contraindicated in patients with known hypersensitivity to eltrombopag or any of its excipients. Caution is advised for individuals with active liver disease, uncontrolled infections, or those receiving strong CYP3A4 inducers, as these conditions may affect safety or efficacy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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