12-24 Hours
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Mircera 75
Radiant Pharmaceuticals Ltd.
Generic: Methoxy Polyethyelene Glycol-Epoetin Beta
Medicine Overview of Mircera 75 75mcg/0.3ml Injection
বাংলা
English
Indication
Anaemia associated with chronic kidney disease
Administration
IV route is recommended for patients receiving hemodialysis because IV route may be less immunogenic
SC: inject in abdomen, arm or thigh
Adult Dose
Patients with chronic renal failure on dialysis Initiate treatment when hemoglobin level 10 g/dL, reduce or interrupt dose, and use lowest dose sufficient to reduce need for RBC transfusions Dose if not currently on ESA therapy: 0.6 mcg/kg IV/SC q2week initially Once hemoglobin has been stabilized, Mircera may be administered once monthly using a dose that is twice that of the every-two-week dose and subsequently titrated as necessary Switching Patients Currently on Other ESA Receiving epoetin 16000 units/week or darbepoetin >80 mcg/week: 360 mcg/qmonth or 180 mcg/q2week IV/SC Anemia Associated with Chronic Renal Failure Do not increase dose more frequently...
... Show moreChild Dose
Safety & efficacy not established
Contraindication
Hypersensitivity. Uncontrolled HTN.
Mode of Action
Methoxy Polyethyelene Glycol-Epoetin Beta is an erythropoietin receptor activator w/ greater activity as well as increased half-life, in contrast to erythropoietin.
Precaution
Discontinue if pure red cell aplasia. Adequate control of BP. Hemoglobinopathies, seizures, platelet level >500 x 109/L. Patients <18 yr.
Lactation: not known if excreted in breast milk, use caution
Side Effect
>10%
Hypertension (13%),Diarrhea (11%),Nasopharyngitis (11%)
1-10%
Headache (9%),Upper respiratory tract infection (9%),Cough (6%),Hypotension (5%),Urinary tract infection (5%),Procedural arteriovenous fistula thrombosis (5%)
Frequency Not Defined
Coronary artery disease,Anemia,Septic shock,Serious cardiovascular and thromboembolic events,Seizures,Immunogenicity related PRCA,Increased mortality and/or tumor progression in cancer patients,Increased mortality,Concomitant termination of other CRF therapy,Stevens-Johnson syndrome,Toxic epidermal necrolysis
Interaction
No interaction studies have been performed. There is no evidence that Mircera alters the metabolism of other medicinal products.
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