Lenalidomide
Lenalidomide
CLINICAL USE
Treatment of multiple myeloma in combination with dexamethasone
DOSE IN NORMAL RENAL FUNCTION
25 mg daily on days 1–21 of a 28 day cycle; reduce dose if patient has neutropenia or thrombocytopenia; see data sheet
PHARMACOKINETICS
Molecular weight                           :259.3 %Protein binding                           :22.7–29.2 %Excreted unchanged in urine     : 65–85 Volume of distribution (L/kg)       :86 litreshalf-life – normal/ESRD (hrs)      :3.5/>9 DOSE IN RENAL IMPAIRMENT
GFR (mL/MIN)
30–50 10 mg daily, increasing to 15 mg after 2 cycles if patient is not responding<30 15 mg every 48 hours DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES
CAPD                :Probably dialysed. 15 mg 2–3 times a week HD                     :Probably dialysed. 15 mg 3 times a week post dialysisHDF/high flux   :Probably dialysed. 15 mg 3 times a week post dialysisCAV/VVHD      :Probably dialysed. Dose as in GFR=30–50 mL/min IMPORTANT DRUG INTERACTIONS
Potentially hazardous interactions with other drugsCardiac glycosides: possibly increases concentration of digoxin ADMINISTRATION
Reconstition
– Route
Oral Rate of Administration
–Comments
– OTHER INFORMATION
May cause acute renal failure – monitor renal function during treatment. Patients with renal impairment are more likely to develop side effects
See how to identify renal failure stages according to GFR calculation
See how to diagnose irreversible renal disease
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