Product Information
Elopag 25 MG (Eltrombopag) is an oral thrombopoietin receptor agonist (TPO-RA) supplied as a 25 mg tablet in 14’s and 28’s packs and registered in Bangladesh. Its active ingredient, eltrombopag, binds to and activates the thrombopoietin receptor (c-Mpl) on megakaryocyte progenitor cells in the bone marrow, stimulating the proliferation and differentiation of megakaryocytes to increase platelet production. Elopag 25 MG (Eltrombopag) is indicated for the treatment of chronic immune (idiopathic) thrombocytopenic purpura (ITP), thrombocytopenia associated with chronic hepatitis C infection, and severe aplastic anemia (SAA) in patients who have had an insufficient response to prior therapies. Eltrombopag works by initiating intracellular signalling pathways that promote megakaryocyte proliferation and differentiation, thereby raising the platelet count and reducing the risk of clinically significant bleeding events. Searching for Elopag 25 MG Eltrombopag in Bangladesh or abroad? Mediaid Pharmacy lists this product within its comprehensive oncology and specialty medicines portfolio, and ships it worldwide.
Basic Product Information of Elopag 25 MG (Eltrombopag)
| Brand Name | Elopag 25 MG (Eltrombopag) |
| Product Name | Elopag 25 |
| Generic Name | Eltrombopag |
| Drug Class | Thrombopoietin Receptor Agonist (TPO-RA), Targeted Platelet-Stimulating Agent |
| Formulation | Tablet |
| Available Strength | 25 mg |
| Available Pack Size | 14’s and 28’s (14 or 28 tablets per pack) |
| Primary Indication | Chronic immune (idiopathic) thrombocytopenic purpura (ITP); thrombocytopenia associated with chronic hepatitis C; severe aplastic anemia (SAA) in patients with insufficient response to prior therapy |
| Registrations | Bangladesh |
| Originator Reference Brand | Promacta / Revolade (eltrombopag) by Novartis |
| Global Supplier | Mediaid Pharmacy, Worldwide Shipping Available |
| Storage Conditions | Store in a dry place away from light and moisture, at the temperature printed on the pack. Keep out of the reach of children. |
How Elopag 25 MG (Eltrombopag) Works: Thrombopoietin Receptor Agonism
Eltrombopag, the active ingredient in Elopag 25 MG, is a selective, orally bioavailable small-molecule agonist of the thrombopoietin receptor (TPO-R), also known as c-Mpl. The thrombopoietin receptor is expressed on the surface of megakaryocyte progenitor cells in the bone marrow. When eltrombopag binds to the transmembrane domain of c-Mpl at a site distinct from where endogenous thrombopoietin (TPO) binds it initiates intracellular signalling through the JAK2 and STAT pathways, which drives megakaryocyte proliferation, differentiation, and maturation, ultimately increasing platelet production and release into the bloodstream.
Because eltrombopag targets a binding site distinct from endogenous TPO, it can act additively with circulating TPO rather than competing with it. This mechanism makes Elopag 25 MG clinically relevant in conditions where platelet counts are dangerously low due to accelerated peripheral destruction (as in chronic ITP), suppressed bone marrow production (as in severe aplastic anemia), or TPO-resistant thrombocytopenia (as in chronic hepatitis C). Patients and oncologists coordinating complex blood disorder management can review the broader range of oncology and haematology medicines available at Mediaid Pharmacy for supportive and companion therapies.
In the pivotal RAISE trial (chronic ITP), eltrombopag produced a platelet response (platelets ≥50 × 10⁹/L) in 59% of patients versus 16% on placebo over the 6-month treatment period (odds ratio 9.61; p <0.0001). Eltrombopag also significantly reduced the rate of clinically significant bleeding events and decreased the need for rescue medication. Notably, a starting dose of 25 mg once daily is the reference label recommendation for East Asian patients including Bangladeshi patients and for those with mild-to-moderate hepatic impairment, making the Elopag 25 MG strength directly relevant to this population.
Approved Indications of Eltrombopag (Reference Label for Elopag 25 MG (Eltrombopag))
Eltrombopag, the active ingredient in Elopag 25 MG, is approved internationally across three distinct clinical settings involving thrombocytopenia. Prescribers in Bangladesh should confirm the exact locally approved indications on the Elopag product label.
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Chronic Immune (Idiopathic) Thrombocytopenic Purpura (ITP) Indicated for adult and paediatric patients (aged 1 year and older) with chronic ITP who have had an insufficient response to corticosteroids, immunoglobulins, or splenectomy. In the RAISE trial, eltrombopag reduced bleeding events and the need for rescue medication over 6 months, with a response rate of 59% versus 16% for placebo. The EXTEND open-label extension study confirmed durable responses maintained for up to 3 years in a subset of patients. |
Severe Aplastic Anemia (SAA) and Hepatitis C-Associated Thrombocytopenia Indicated for patients with severe aplastic anemia (SAA) who have had an insufficient response to immunosuppressive therapy, and in combination with standard immunosuppression (anti-thymocyte globulin and ciclosporin) for treatment-naïve SAA. Eltrombopag is also indicated for thrombocytopenia in adult patients with chronic hepatitis C to allow initiation and maintenance of interferon-based antiviral therapy, where platelet levels otherwise preclude treatment. |
Key Clinical Benefits of Elopag 25 MG (Eltrombopag)
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Significant Platelet Response in Chronic ITP In the RAISE trial, eltrombopag produced a platelet response in 59% of patients versus 16% on placebo, demonstrating a 9.61-fold greater odds of achieving a clinically meaningful platelet count (≥50 × 10⁹/L) that reduces the risk of spontaneous bleeding. |
Effective 25 mg Starting Dose for East Asian and Hepatically Impaired Patients The reference label specifies 25 mg once daily as the recommended starting dose for patients of East Asian ancestry including Bangladeshi patients and for those with mild-to-moderate hepatic impairment. This makes the Elopag 25 MG tablet strength directly aligned with clinical dosing guidance for this patient population. |
Durable Long-Term Response in ITP and SAA The EXTEND open-label extension trial demonstrated that responders to eltrombopag maintained platelet counts above 50 × 10⁹/L for a median of 73 weeks. In treatment-naïve SAA, eltrombopag combined with immunosuppression achieved a complete or partial response rate of approximately 94% in a Phase II trial, substantially higher than historical immunosuppression-alone benchmarks. |
Dosage and Administration of Elopag 25 MG (Eltrombopag)
General Administration Rule: Eltrombopag must be taken on an empty stomach at least 2 hours before or 4 hours after any food, drink, or medication containing polyvalent cations (calcium-rich dairy products, antacids containing aluminum, magnesium, or calcium, iron supplements, selenium, or zinc). These cations chelate eltrombopag in the gastrointestinal tract and can reduce systemic drug exposure by up to 70%. Always swallow tablets whole with plain water.
Chronic ITP East Asian Patients and Hepatic Impairment: The reference label recommends a starting dose of 25 mg once daily for adult patients of East Asian ancestry (including Bangladeshi patients) and for patients with mild-to-moderate hepatic impairment. For other adults, the standard starting dose is 50 mg once daily. The dose is adjusted in 25 mg increments every 2 weeks based on the platelet count response, up to a maximum of 75 mg daily. The lowest dose that achieves and maintains a platelet count ≥50 × 10⁹/L is the target.
Severe Aplastic Anemia (SAA): In combination with immunosuppressive therapy, eltrombopag is typically started at 150 mg once daily in adults (75 mg in East Asian adults). In refractory SAA, the dose and duration are determined by the treating haematologist based on response and tolerability.
Hepatitis C-Associated Thrombocytopenia: The starting dose is 25 mg once daily, titrated based on platelet count to allow antiviral therapy initiation, up to a maximum of 100 mg daily. Eltrombopag is discontinued when antiviral therapy concludes.
Missed Dose: If a dose is missed, the patient should take it on the same day and resume the normal schedule the next day. Two doses must not be taken on the same day to compensate for a missed dose.
Paediatric Use (ITP): For children aged 1–5 years, the starting dose is 25 mg once daily. For children aged 6–17 years, 50 mg once daily is the standard start, with 25 mg for East Asian patients in this age group. All paediatric dosing must be directed by a specialist.
Clinical Monitoring Requirements During Elopag 25 MG (Eltrombopag) Treatment
Regular monitoring is mandatory throughout eltrombopag therapy. Hepatotoxicity is the most clinically significant non-haematologic risk. The reference label requires liver function tests (ALT, AST, and bilirubin) at baseline, every 2 weeks during the dose-adjustment phase, and monthly once a stable dose is established. Eltrombopag must be discontinued if ALT rises to ≥3× the upper limit of normal with signs of hepatic dysfunction, is ≥3× baseline in patients with elevated pre-treatment values, or is ≥5× the upper limit of normal and persistent.
Platelet count monitoring is required weekly during dose initiation and adjustment, then monthly once stable. Maintaining the platelet count in the target range (50–200 × 10⁹/L for ITP) is essential, because supratherapeutic platelet counts increase the risk of thromboembolic events including deep vein thrombosis and portal vein thrombosis. Peripheral blood smears and complete blood counts should be reviewed monthly for morphological changes consistent with bone marrow fibrosis, an uncommon but serious complication. Ophthalmic examination for cataracts should be performed at baseline and periodically during treatment, since lens changes have been reported with eltrombopag.
Drug Interactions and Important Safety Information for Elopag 25 MG (Eltrombopag)
The most clinically important interaction for eltrombopag is chelation by polyvalent cations. Foods and medications containing calcium (dairy products, calcium-fortified juices, antacids), aluminum, magnesium, iron, selenium, or zinc bind eltrombopag in the gastrointestinal tract and can reduce drug absorption by up to 70%. Patients must take Elopag 25 MG tablets on an empty stomach, at least 2 hours before or 4 hours after any polyvalent cation-containing product. This is the single most important administration instruction for maintaining adequate drug exposure.
Eltrombopag is an inhibitor of the drug transporters OATP1B1 and OATP1B3. Co-administration with rosuvastatin increases rosuvastatin plasma exposure by approximately 55%; the rosuvastatin dose should be reduced and patients monitored for statin-related adverse effects. Eltrombopag is also a substrate of CYP1A2 and CYP2C8, so strong inhibitors of these enzymes (ciprofloxacin, fluvoxamine, gemfibrozil) may increase eltrombopag exposure. Patients must provide their prescribing physician with a complete list of all current medications prescription, over-the-counter, and herbal before starting eltrombopag. Anticoagulants and antiplatelet agents should be used cautiously because excessive platelet elevation increases clot risk, while excess platelet suppression increases bleeding risk if the dose is not titrated correctly.
Side Effects and Precautions of Elopag 25 MG (Eltrombopag)
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Common Side Effects Nausea, vomiting, and abdominal pain Elevated liver enzymes (ALT and AST) Headache and dizziness Fatigue and influenza-like symptoms Diarrhoea and constipation Upper respiratory tract infection Alopecia (hair thinning) Myalgia (muscle pain) and arthralgia (joint pain) Cataract development or worsening Decreased appetite and weight changes |
Serious Warnings and Precautions Hepatotoxicity: monitor liver function tests (ALT, AST, bilirubin) at baseline, every 2 weeks during dose adjustment, then monthly. Discontinue if serious hepatic dysfunction occurs. Thromboembolic events: excessive platelet elevation can cause DVT, pulmonary embolism, or portal vein thrombosis. Titrate to the minimum effective dose and monitor platelet count. Bone marrow fibrosis: review peripheral blood smears monthly for morphological changes and discontinue if fibrosis is confirmed on biopsy. Cataracts: baseline and periodic ophthalmic examination is required throughout treatment. Embryo-fetal toxicity: not recommended during pregnancy. Effective contraception is required during treatment and for at least 7 days after the final dose. |
Who Should Use Elopag 25 MG (Eltrombopag)?
Elopag 25 MG (Eltrombopag) is prescribed for adults and paediatric patients (aged 1 year and older) with chronic immune thrombocytopenic purpura (ITP) who have not responded adequately to corticosteroids, immunoglobulins, or splenectomy. It is also prescribed for adults with severe aplastic anemia (SAA) who did not respond to immunosuppressive therapy, or as part of first-line combination immunosuppression for treatment-naïve SAA. The 25 mg starting dose is the reference label recommendation for East Asian patients including Bangladeshi patients and for those with mild-to-moderate hepatic impairment, making Elopag 25 MG particularly well-suited to clinical practice in Bangladesh. Prescribers assess baseline liver function, platelet count, blood smear morphology, and eye health before initiating treatment. Elopag 25 MG is prescribed by haematologists and specialist physicians experienced with thrombopoietin receptor agonist therapy. For patients who need broader haematology and cancer care support, Mediaid Pharmacy’s oncology specialty medicines range offers a wide selection of targeted and supportive therapies.
Global Supplier: Mediaid Pharmacy Worldwide Shipping for Elopag 25 MG (Eltrombopag)
Mediaid Pharmacy is a Dhaka-based supplier of oncology and specialty medicines with worldwide shipping. Elopag 25 MG (Eltrombopag) is available in 14’s and 28’s tablet packs, and orders are supported by pricing quotations, stock confirmation, documentation, and delivery tracking. Hospitals, distributors, and patients can contact the Mediaid Pharmacy team through WhatsApp, phone, or WeChat for all questions about Elopag 25 MG Eltrombopag availability, pricing, and international delivery. Buyers who need several haematology or oncology medicines in one consignment can browse the full oncology medicine collection before requesting a combined quotation.
Why Choose Elopag 25 MG (Eltrombopag) from Mediaid Pharmacy?
Elopag 25 MG (Eltrombopag) gives haematology and specialist teams a Bangladesh-registered eltrombopag tablet for ITP, severe aplastic anemia, and hepatitis C-associated thrombocytopenia, backed by the clinical evidence generated in the RAISE, EXTEND, and SAA Phase II/III trials. The 25 mg strength is the guideline-recommended starting dose for East Asian including Bangladeshi patients and those with hepatic impairment, reflecting precise clinical alignment with the local patient population. Mediaid Pharmacy supplies Elopag 25 MG in 14’s and 28’s packs with clear product specifications, direct specialist support, and worldwide shipping. Every order starts with a prescription-based enquiry, which keeps supply aligned with clinical need. To compare eltrombopag with other targeted haematology agents or to source additional cancer and blood disorder therapies, visit the Mediaid Pharmacy oncology medicines section, then contact our team for a personalised quotation.
Frequently Asked Questions About Elopag 25 MG (Eltrombopag)
What is Elopag 25 MG (Eltrombopag) used for?
Elopag 25 MG (Eltrombopag) is an oral thrombopoietin receptor agonist (TPO-RA) used to treat chronic immune (idiopathic) thrombocytopenic purpura (ITP) in adults and children aged 1 year and older who have not responded sufficiently to corticosteroids, immunoglobulins, or splenectomy. It is also used for severe aplastic anemia (SAA) in patients with an insufficient response to immunosuppressive therapy, and for thrombocytopenia in adult patients with chronic hepatitis C to allow antiviral treatment to proceed. Eltrombopag works by activating the thrombopoietin receptor on bone marrow cells to stimulate platelet production.
What is the generic name of Elopag?
The generic name of Elopag is eltrombopag. Elopag 25 MG is a tablet formulation available in 14’s and 28’s packs and registered in Bangladesh. The originator reference brand for eltrombopag is Promacta (United States) and Revolade (Europe and other markets), both by Novartis.
What is the correct starting dose of Elopag 25 MG (Eltrombopag) for Bangladeshi patients?
The dose must be determined by your treating haematologist or specialist physician. The reference label for eltrombopag specifically recommends a starting dose of 25 mg once daily for patients of East Asian ancestry including Bangladeshi patients and for patients with mild-to-moderate hepatic impairment with chronic ITP. The dose is then adjusted in 25 mg increments every 2 weeks based on platelet count response, up to a maximum of 75 mg daily. Never change your dose without medical guidance.
What strengths and pack sizes is Elopag available in?
Elopag is available as a 25 mg tablet in pack sizes of 14 tablets and 28 tablets. Contact Mediaid Pharmacy for current stock availability and worldwide shipping details.
What are the side effects of Elopag 25 MG (Eltrombopag)?
Common side effects of eltrombopag include nausea, elevated liver enzymes (ALT/AST), headache, fatigue, diarrhoea, upper respiratory tract infections, cataract, and myalgia. Serious but less common effects include clinically significant hepatotoxicity, thromboembolic events (such as deep vein thrombosis and portal vein thrombosis due to excessive platelet elevation), bone marrow fibrosis, and embryo-fetal toxicity. Regular liver function tests, platelet counts, blood smear reviews, and eye examinations are mandatory throughout treatment. Consult your prescribing physician about your individual risk profile.
Why must eltrombopag be taken on an empty stomach?
Eltrombopag chelates (binds to) polyvalent cations present in foods and medications, including calcium in dairy products, magnesium and aluminum in antacids, iron in supplements, and selenium and zinc. Chelation prevents eltrombopag from being absorbed through the gastrointestinal wall and can reduce systemic drug exposure by up to 70%. Elopag 25 MG must be taken at least 2 hours before or 4 hours after any polyvalent cation-containing food, drink, or medicine, and swallowed with plain water only.
How often are blood tests and liver function tests needed during eltrombopag treatment?
The reference label recommends liver function tests (ALT, AST, and bilirubin) at baseline, every 2 weeks during the dose-adjustment phase, and monthly once a stable dose is reached. Platelet counts should be monitored weekly during initiation and dose adjustment, then monthly when stable. Monthly peripheral blood smears are required to detect early signs of bone marrow fibrosis, and regular ophthalmic examinations for cataracts are required throughout treatment.
Is Elopag 25 MG safe during pregnancy or while breastfeeding?
No. Eltrombopag is not recommended during pregnancy as it may cause fetal harm. Women of reproductive potential must use effective contraception during treatment and for at least 7 days after the final dose. Breastfeeding is not advised during eltrombopag treatment. Speak with your prescribing physician before starting treatment if you are pregnant, planning pregnancy, or breastfeeding.
Can I order Elopag 25 MG (Eltrombopag) online with worldwide shipping?
Yes. Mediaid Pharmacy supplies Elopag 25 MG (Eltrombopag) to patients and healthcare providers globally. Contact Mediaid Pharmacy via WhatsApp, phone, or WeChat at +8801773428128, or email info@mediaidpharmacy.com for pricing, stock availability, and delivery details for your country.
Order Elopag 25 MG (Eltrombopag) with Worldwide Shipping
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