GNH USA

Europe — EMA

Mylatabi (Eltrombopag)

GNH USA supplies Mylatabi (Eltrombopag), a thrombopoietin receptor agonist for chronic immune thrombocytopenia, aplastic anemia, and severe thrombocytopenia

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What is Eltrombopag?

Eltrombopag, the active ingredient in Mylatabi, is a thrombopoietin receptor agonist presented as an oral tablet for oral use. It is indicated for chronic immune thrombocytopenia, aplastic anemia, and severe thrombocytopenia associated with chronic hepatitis C. GNH USA supplies Mylatabi as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

What is Eltrombopag used for?

Eltrombopag acts on the thrombopoietin pathway to increase platelet production in several hematologic disorders. - Chronic immune thrombocytopenia (ITP): raises platelet counts in patients with persistent low platelet levels. - Aplastic anemia: stimulates residual marrow to produce more platelets, improving thrombocytopenia. - Severe thrombocytopenia associated with chronic hepatitis C: helps achieve safer platelet levels during antiviral therapy.

What are the side effects of Eltrombopag?

Eltrombopag may cause a range of adverse reactions.

Common Side Effects: - Headache: mild to moderate intensity. - Nausea: occasional, often transient. - Diarrhea: may be watery or loose. - Fatigue: general feeling of tiredness. - Elevated liver enzymes: mild transaminase increases. - Dyspepsia: indigestion or stomach discomfort.

Serious or Rare Side Effects: - Thromboembolic events: clot formation in veins or arteries. - Severe liver injury: marked elevation of hepatic enzymes or hepatitis. - Cataract formation: lens opacity reported with long‑term use. - Severe neutropenia: marked reduction in neutrophil count. - Hypersensitivity reactions: rash, angioedema, or anaphylaxis.

What precautions apply to Eltrombopag?

Before initiating therapy, several safety considerations should be addressed. - Monitor platelet counts: adjust therapy based on response and target levels. - Assess liver function: obtain baseline and periodic transaminases. - Screen for thrombotic risk: avoid in patients with active or uncontrolled thrombosis. - Use in pregnancy only if benefits outweigh risks: limited data available. - Store at ambient temperature below 25°C: keep in the original pack, protect from moisture.

What does Eltrombopag interact with?

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

Major Interactions (Avoid): - Antacids containing aluminum or magnesium: markedly reduce oral absorption of eltrombopag. - Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): may lower plasma concentrations and diminish effect.

Moderate Interactions (Monitor Closely):\n- Moderate CYP3A4 inhibitors (e.g., fluconazole, erythromycin): can increase eltrombopag levels. - Concurrent use with other myelosuppressive agents: requires close monitoring of blood counts. - Herbal supplements such as St. John's wort: may alter metabolism and affect drug exposure.

Frequently asked questions

What is Mylatabi used for?+
Mylatabi contains the active ingredient eltrombopag and is prescribed to increase platelet counts in patients with chronic immune thrombocytopenia, aplastic anemia, and severe thrombocytopenia associated with chronic hepatitis C infection.
How does eltrombopag work?+
Eltrombopag is a small‑molecule agonist of the thrombopoietin receptor (c‑Mpl). By binding to this receptor on megakaryocyte precursors, it stimulates their proliferation and maturation, leading to enhanced platelet production in the bone marrow.
What is the usual dose of Mylatabi?+
The dose of Mylatabi is individualized by the prescribing clinician based on the patient’s platelet count, underlying condition, and response to therapy. Specific dosing regimens are determined by the treating physician.
Is Mylatabi safe in pregnancy or breastfeeding?+
Safety data for eltrombopag during pregnancy and lactation are limited. It should only be used if the potential benefit justifies any potential risk to the fetus or infant, and the decision must be made by the healthcare provider.
How do I order Mylatabi from GNH USA?+
To order, submit an enquiry on the Mylatabi product page at gnh-usa.com, indicating the required quantity. GNH USA works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details, and any required import documentation.
How does Mylatabi compare with the main alternative drug?+
The primary alternative is romiplostim, a peptide thrombopoietin receptor agonist administered subcutaneously. Eltrombopag (Mylatabi) is taken orally, offering greater convenience, whereas romiplostim requires injection. Both aim to raise platelet counts, but their efficacy, safety profiles, and administration routes differ, influencing clinician choice.
How should Mylatabi be stored and handled?+
Store Mylatabi tablets at ambient temperature below 25 °C in the original container, protected from moisture and direct sunlight. Do not keep in bathrooms or near heat sources, and discard any tablets that are past their expiry date.
How is Mylatabi administered?+
Mylatabi is taken orally, usually once daily on an empty stomach—at least two hours before or after meals—to maximize absorption. Swallow the tablet whole with a glass of water; do not crush, chew, or split the tablet.
What are the most serious risks to watch for while taking Mylatabi?+
Serious adverse events include thromboembolic complications, severe liver injury, and rare cases of cataract formation. Patients should be monitored for signs of clotting, liver dysfunction (elevated enzymes, jaundice), and visual changes, and any concerning symptoms should be reported promptly.
Who should not use Mylatabi?+
Mylatabi is contraindicated in individuals with known hypersensitivity to eltrombopag, active uncontrolled thrombotic disease, or severe hepatic impairment. It should also be used with caution in pediatric patients and those with a history of malignancy. A healthcare professional should evaluate suitability before prescribing.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Eltrombopag
Route
Oral Use
Manufacturer
Tillomed Malta Ltd
Origin
EU

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