Eporen 4000 Pfs I.U Inj

Eporen 4000 Pfs I.U Inj belongs to the group of hormones used in the treatment of chronic anaemia and anaemic states seen in kidney disease, cancers, patients on chemotherapy, bone marrow disorders and in those due to undergo major bone surgery. Anaemia refers to low blood counts due to a deficiency of blood component haemoglobin, resulting in a reduced oxygen-carrying capacity of the blood.

Eporen 4000 Pfs I.U Inj contains Recombinant Human Erythropoietin Alfa that works by stimulating the bone marrow to produce more red blood cells, thereby correcting any low blood counts and anaemia.

In some cases, Eporen 4000 Pfs I.U Inj may cause certain common side effects such as vomiting, diarrhoea, fever, and nasal congestion. Most of these side effects do not require medical attention and will resolve gradually over time. However, you are advised to talk to your doctor if you experience these side effects consistently.

Please inform the doctor of your detailed medical history including hypertension, heart disease, heart attack, stroke, epilepsy, cancer, liver disease, thromboembolism, porphyria and/or pure red cell aplasia (where the bone marrow cannot produce enough RBC’s). Consult your doctor before taking Eporen 4000 Pfs I.U Inj during pregnancy and nursing.

Eporen 4000 Pfs I.U Inj is a blood hormone. It contains Recombinant Human Erythropoietin Alfa used to treat anaemia caused by chronic diseases and anaemia related to kidney disease, cancers, bone marrow disorders, chemotherapy, children and adults on dialysis, and in those due to undergo major bone surgery. Eporen 4000 Pfs I.U Inj stimulates the bone marrow to produce more red blood cells. In addition, it also corrects any dysregulated erythropoiesis (RBC formation) and remedies the formation of any defunct precursors of RBC’s, paving the way for healthy red blood cell production. Clinically, Eporen 4000 Pfs I.U Inj causes a direct increase in haemoglobin values and reduces the rates and requirement of blood transfusion.

Inform the doctor in case of an allergy to any of its components. Proceed with caution in case of a latex allergy. Please inform the doctor of your detailed medical history including hypertension, heart disease, myocardial infarction, stroke, epilepsy, head and neck cancers, liver disease, thromboembolism, porphyria and/or pure red cell aplasia (where the bone marrow cannot produce enough RBC’s). Inform your doctor of any medicines you may be taking especially if you are on any immunosuppressants, blood thinners or blood stimulants. Please consult your doctor before taking Eporen 4000 Pfs I.U Inj during pregnancy and nursing.

• Eporen 4000 Pfs I.U Inj should never be given intramuscularly.
• Do not self-inject before proper training.
• Exercise caution in case of a history of allergic disorders or a known allergy to latex, or any of the components of Eporen 4000 Pfs I.U Inj.
• Please inform the doctor immediately if you notice any anaphylaxis (allergy, skin changes, difficulty in breathing, anxiety, confusion, dizziness etc) post-injection.
• Your doctor may advise blood tests regularly to check your need and tolerance of Eporen 4000 Pfs I.U Inj.