Eralfon 40000 IU 1 ml syringe with needle protection device
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Anemia
Active ingredient
Epoetin alfa
Composition
1 syringe contains 40000 IU of recombinant human erythropoietin
Excipients:
Sodium chloride – 5.84 mg,
sodium citrate pentasquihydrate – 5.8 mg or sodium citrate dihydrate – 4.776 mg,
albumin solution (in terms of dry albumin) – 2.5 mg,
citric acid monohydrate – 0.057 mg,
d/i water – up to 1 ml.
How to take, the dosage
Administered by injection by injection or intravenously. When changing the method of administration the drug is administered in the same dose, then the dose is adjusted if necessary (to achieve the same therapeutic effect when administered p/v the dose is 20-30% lower than when administered intravenously).
Interaction
Decreases cyclosporine concentration due to increased binding to red blood cells (cyclosporine dose adjustment may be necessary).
Special Instructions
During treatment, BP should be monitored weekly and general blood counts (including platelets, hematocrit, and ferritin) should be performed. In pre- and postoperative period Hb should be monitored more frequently if baseline was less than 140 g/l.
Contraindications
Absolute contraindications have not been identified.
Side effects
In the beginning of treatment there may be flu-like symptoms: dizziness, somnolence, feverishness, headache, myalgia, arthralgia.
Systems: dose-dependent increase of BP, worsening of arterial hypertension course (most frequently in patients with chronic renal failure); in single cases – hypertensive crisis, sharp increase of BP with encephalopathy symptoms (headache, mental confusion) and generalized tonic-clonic convulsions.
Hematopoietic organs: thrombocytosis, in some cases – thrombosis of shunt or arteriovenous fistula (including patients on hemodialysis with a tendency to arterial hypotension or with aneurysm, stenosis), aplasia of red blood cell generation.
Allergic reactions: skin rash (mild to moderately expressed), eczema, urticaria, pruritus, angioedema.
Local reactions: hyperemia, burning, mild to moderate soreness at the injection site (more common with pneumonic administration).
Laboratory findings: decreased serum ferritin concentration, in uremia – hyperkalemia, hyperphosphatemia.
Others: complications associated with respiratory distress or with a decrease in BP, immune reactions (induction of antibody formation), exacerbation of porphyria.
Overdose
Symptoms: intensification of side effects.
Similarities
Binocrit
Weight | 0.028 kg |
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Shelf life | 2 years |
Conditions of storage | At a temperature of 2° to 8° C. |
Manufacturer | PharmFirm Sotex, Russia |
Medication form | solution for injections and infusions |
Brand | PharmFirm Sotex |
Other forms…
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