Elopag Tablet 50 mg (promoted under the brand name Promacta, among others) is an oral chemotherapy drug prescribed for the treatment of thrombocytopenia—a condition associated with low platelet counts in the blood.
Elopag Tablet 50 mg is primarily prescribed for people suffering from thrombocytopenia who do not respond to other standard treatments. It is also used for enhancing platelet counts in people suffering from hepatitis C, aplastic anemia, and hereditary thrombocytopenia.
| Brand Name | Elopag |
|---|---|
| Type | Tablet |
| Weight | 50 mg |
| Generic | Eltrombopag Olamine |
| Manufacturer | Everest Pharmaceuticals Ltd. |
| Available in | English বাংলা |
Elopag Tablet 50 mg binds to and activates the thrombopoietin receptor site on megakaryocyte progenitor cells, which helps in stimulating the proliferation and maturation of megakaryocytes to release more platelets in the blood. This ultimately increases platelet counts.
Elopag Tablet 50 mg typically takes about 7 to 14 days to work. Patients may begin to see platelet count increase within 4-5 days but it is better to consult a doctor to check platelet count at 7 to14 days at its maximum effectiveness.
Elopag Tablet 50 mg is rapidly and completely absorbed from the gastrointestinal tract. Peak plasma concentrations are reached about 1-3 hours after oral administration.
Elopag Tablet 50 mg is mainly excreted in feces as metabolites and about 3 to 5 percent is excreted in the urine unchanged.
The recommended starting dose of eltrombopag olamine is 50 mg once per day orally.
Elopag Tablet 50 mg should be taken with or without food, not to exceed 50 mg once per day. It should be taken at least one hour before or two hours after a meal.
Some common side effects associated with Elopag Tablet 50 mg include nausea, fatigue, headache, abdominal pain, influenza-like symptoms, and constipation.
In case of an overdose of Elopag Tablet 50 mg, it can cause severe hepatic toxicity, leading to liver damage. If overdose is confirmed, the patient should seek immediate medical treatment.
Elopag Tablet 50 mg should not be administered to patients with hypersensitivity to the drug and its components, or severe hepatic impairment.
Elopag Tablet 50 mg should not be combined with drugs that inhibit CYP3A4 and P-glycoprotein transporter, as well as drugs that induce CYP3A4 and P-glycoprotein transporter.
Elopag Tablet 50 mg should not be administered to patients with severe hepatic impairment since it can lead to serious health complications such as liver failure or death.
Elopag Tablet 50 mg may interact with several drugs such as simvastatin, teriflunomide, procainamide, quinidine, methotrexate and mifepristone.
Elopag Tablet 50 mg is not known to interact with food. However, it should be taken on an empty stomach or at least one hour before or two hours after a meal for better absorption.
Elopag Tablet 50 mg should not be used during pregnancy unless the potential benefit justifies the risk to the foetus.
Elopag Tablet 50 mg has not been tested in lactating women, and therefore its use is not recommended.
In case of an acute overdose of Elopag Tablet 50 mg, it can cause severe hepatic toxicity, leading to liver damage. If overdose is confirmed, the patient should seek immediate medical treatment.
Elopag Tablet 50 mg is contraindicated in patients with hypersensitivity to the drug and its components, as well as in patients with severe hepatic impairment.
Elopag Tablet 50 mg should be taken as directed by the health care provider. It should be taken once daily with or without food, not to exceed 50 mg per day. It should be taken at least one hour before or two hours after a meal, for better absorption.
Elopag Tablet 50 mg should be stored at room temperature, away from light and moisture.
The volume of distribution of Elopag Tablet 50 mg is 0.8 L/kg.
The half-life of Elopag Tablet 50 mg is approximately 13 hours.
The average clearance of Elopag Tablet 50 mg is 18.2 L/h.
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