Informational only — Not medical advice. Always consult a licensed healthcare provider.

Community data Updated 22 hours ago

Indications

Erythropoietin Beta is used to treat symptomatic anemia associated with chronic kidney disease (CKD) in patients on dialysis. It is also used for symptomatic renal anemia in patients who are not yet undergoing dialysis. A third use is the prevention of anemia of prematurity in infants with a birth weight of 750 to 1500 g and a gestational age of less than 34 weeks. Recormon is used for those same three conditions: symptomatic anemia associated with CKD in patients on dialysis, symptomatic renal anemia in patients not yet undergoing dialysis, and prevention of anemia of prematurity in infants with a birth weight of 750 to 1500 g and a gestational age of less than 34 weeks. It is also used to treat symptomatic anemia in adult patients with non-myeloid malignancies who are receiving chemotherapy. Another use is increasing the yield of autologous blood from patients in a pre-donation programme. For this use, the benefit has to be balanced against the reported increased risk of thromboembolic events. Treatment should only be given to patients with moderate anemia (Hb 10 to 13 g/dl [6.21 to 8.07 mmol/l], no iron deficiency) if blood conserving procedures are not available or are not enough, and the scheduled major elective surgery needs a large volume of blood (4 or more units of blood for females or 5 or more units for males).

⚠️ Always consult a registered physician before taking any medicine.

Pharmacology

Erythropoietin beta has the same amino acid and carbohydrate make-up as the erythropoietin that has been isolated from the urine of anemic patients. Erythropoietin is a glycoprotein. As a growth factor, it mainly stimulates the formation of erythrocytes from their committed progenitors. It acts as a mitosis-stimulating factor and as a differentiation hormone.

Erythropoietin is a glycoprotein that stimulates the formation of erythrocytes from its committed progenitors, and it works as a mitosis-stimulating factor and differentiation hormone.

Pregnancy & Breastfeeding

Pregnancy: Animal studies don't point to any direct or indirect harmful effects on pregnancy, embryonal/fetal development, parturition or postnatal development. For epoetin beta, all the safety information on exposure to Erythropoietin Beta during pregnancy comes from post-marketing experience. A review of the post-marketing data available shows no evidence of a causal link between treatment with Erythropoietin Beta and harmful effects on pregnancy, embryonal/fetal development or postnatal development. But there are no clinical study data, so caution should be used when prescribing to pregnant women.

Lactation: Experience in human lactation is limited. Endogeneous erythropoietin is excreted in breast milk and is readily absorbed by the neonatal gastrointestinal tract. Whether to continue or stop breastfeeding, or to continue or stop therapy with epoetin beta, should be decided by weighing the benefit of breastfeeding to the child against the benefit of epoetin beta therapy to the woman.

⚠️ Talk to your doctor before taking any medicine during pregnancy or while breastfeeding.

Dosage Reference

⚠️ Reference ranges from official sources only. Consult your doctor for personalized dosing.

Adults: Erythropoietin Beta treatment should be started by a physician who has experience with the indications mentioned above. Anaphylactoid reactions have been seen in isolated cases, so the first dose should be given under medical supervision. Substitution by any other biological medicinal product needs the consent of the prescribing physician. The Erythropoietin Beta pre-filled syringe is ready for use. Inject only a solution that is clear or slightly opalescent, colourless and practically free of visible particles. The syringe is sterile but unpreserved, so never give more than one dose from a single syringe. Treatment of anemic patients with chronic renal failure: the solution can be given subcutaneously or intravenously. For intravenous use, inject it over approximately 2 minutes. In hemodialysis patients, for example, this can be done through the arteriovenous fistula at the end of dialysis. In non-hemodialysed patients, subcutaneous administration should always be preferred, to avoid puncture of peripheral veins. The recommended hemoglobin target is 10 to 12 g/dl. If the patient has hypertension, or existing cardiovascular, cerebrovascular or peripheral vascular diseases, the target hemoglobin should be decided individually. Hemoglobin should be checked at regular intervals (e.g. every two to four weeks) until it is stable, and periodically after that. Treatment with Erythropoietin Beta is divided into two stages. Correction phase Subcutaneous administration: the initial dosage is 3 x 20 IU/kg body weight per week. If the Hb increase is not adequate (Hb <1.5 g/L per week), the dosage may be raised every 4 weeks by 3 X 20 IU/kg body weight/week. The weekly dose can also be divided into daily doses. Intravenous administration: the initial dosage is 3 x 40 IU/kg per week. After 4 weeks it may be raised to 80 IU/kg three times per week, and then by further increments of 20 IU/kg three times per week if needed, at monthly intervals. For both routes, the maximum dose should not exceed 720 IU/kg per week.

Side Effects & Interactions

Side Effects

No side-effect data recorded yet.