moxisylyte
CLINICAL USE
Primary Raynaud’s syndrome
DOSE IN NORMAL RENAL FUNCTION
40–80 mg 4 times daily
PHARMACOKINETICS
Molecular weight                           :315.8 %Protein binding                           :No data %Excreted unchanged in urine     : <1 Volume of distribution (L/kg)       :Low1half-life – normal/ESRD (hrs)      :1–2 DOSE IN RENAL IMPAIRMENT
GFR (mL/MIN)
25–50 Dose as in normal renal function10–25 Dose as in normal renal function <10           : Dose as in normal renal function DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES
CAPD                :Unlikely to be dialysed. Dose as in normal renal function HD                     :Unlikely to be dialysed. Dose as in normal renal functionHDF/high flux   :Unlikely to be dialysed. Dose as in normal renal functionCAV/VVHD      :Unlikely to be dialysed. Dose as in normal renal function IMPORTANT DRUG INTERACTIONS
Potentially hazardous interactions with other drugsAlpha-blockers: possibly severe postural hypotension when given in combinationBeta-blockers: possibly severe postural hypotension when given in combination ADMINISTRATION
Reconstition
– Route
Oral Rate of Administration
–Comments
– OTHER INFORMATION
Theoretically may decrease insulin requirements in diabetics
See how to identify renal failure stages according to GFR calculation
See how to diagnose irreversible renal disease
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