DrugInfoSys

Epoetin

Also known as: Human Erythropoitin

Drug #279

Epoetin is a recombinant human erythropoitin, a 165 amino acid glycoprotein produced by Chinese hamster ovary cells into which a human erythropoietin gene has been inserted. Epoetin is used as an antianemic. It increases red blood cells (RBCs) production in body and effective in the treatment of anemia associated with chronic renal failure or dialysis or anemia caused by AZT in HIV-infected persons. Epoetin is administered intravenously or subcutaneously.

Primary Characteristics

Epoetin is also known as Human Erythropoitin.

It is of Natural origin and belongs to Glycoprotein.

It belongs to Erythropoietin agonist pharmacological group on the basis of mechanism of action and also classified in Colony Stimulating Factor pharmacological group. It is also classified under Hematological Agents .

Molecular Weight: 30400 · Solubility in Water: soluble · Non-proprietary name: Epoetin.

Molecular structure of Epoetin

Pharmacokinetics

Distribution: Epoetin has a volume of distribution is 49.3 ml/kg.

Elimination: it is metabolised via low via liver, plasma half-life is 3.8-5.6 hr, renal excretion is 10%.

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Indications

Epoetin is primarily indicated in conditions like Acceleration of myeloid recovery following bone marrow transplantation, Anaemia.

Epoetin is also indicated for secondary conditions like Orthostatic hypotension.

Contraindications

Epoetin is contraindicated in conditions like Erythroid leukaemia, Uncontrolled hypertension.

Dosage

Epoetin's dosage details are as follows:

DoseSingle DoseFrequencyRouteInstructions
Adult Dosage
187.5 IU/ kg187.5 IU/ kgIVMaintenance for thrice a Week
62.5 IU/ kg62.5 IU/ kgIV,SCInitially for thrice a Week
Paediatric Dosage (20kg)
50 IU/kg50 IU/kgEvery 8hIntra Venous Initially per week, As required
105 IU/kg105 IU/kgEvery 8hIntra Venous Maintenance, As Required
Neonatal Dosage (3kg)
50 IU/kg50 IU/kgEvery 8hIntravenousInitially 3 times per week
112.5 IU/kg112.5 IU/kgEvery 8hIntravenousMaintenance, as required

Drug Interactions

Unknown5 interactions

Always consult your physician for the change of dose regimen or an alternative drug of choice that may strictly be required.

Side Effects

Epoetin produces potentially life-threatening effects which include Hyperkalemia , Grand mal seizures, Increased mean arterial BP, Thrombosis. Careful monitoring is needed with proper medical management.

Epoetin is known to cause more or less tolerable side effects which are usually transient. These include Dizziness, Headache, Muscular aches, Shivering .

Warnings / Precautions

Epoetin should be used with caution in pregnant or nursing women only if clearly needed. It should be used with caution in patients with history of blood clots, heart or blood vessel disease, high blood pressure, porphyria, seizures or problems with bones. This drug may not work if patient have sickle cell anemia. Evaluation of iron stores, by measurement of serum iron, iron-binding capacity, and ferritin, should be undertaken before initiation of treatment.

Interference in Pathology

Epoetin may interfere in the diagnosis of Serum Tests for Uric Acid , Complete blood cell count.

Available Brands

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Storage Conditions

Epoetin should be stored Inj (reconstituted soln).

Drug Classification

  1. 1.10.4Anabolics & hematopoietics

Manufacturers