inositol nicotinate
inositol nicotinate
CLINICAL USE
Peripheral vascular disease
DOSE IN NORMAL RENAL FUNCTION
3 g daily in 2–3 divided doses, maximum 4 g daily
PHARMACOKINETICS
Molecular weight                           :810.7 %Protein binding                           :High %Excreted unchanged in urine     : No data Volume of distribution (L/kg)       :No datahalf-life – normal/ESRD (hrs)      :24 DOSE IN RENAL IMPAIRMENT
GFR (mL/MIN)
30–50 Dose as in normal renal function10–30 Dose as in normal renal function <10           : Dose as in normal renal function DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES
CAPD                :Unknown dialysability. Dose as in normal renal function HD                     :Unknown dialysability. Dose as in normal renal functionHDF/high flux   :Unknown dialysability. Dose as in normal renal functionCAV/VVHD      :Unknown dialysability. Dose as in normal renal function IMPORTANT DRUG INTERACTIONS
Potentially hazardous interactions with other drugsNone known ADMINISTRATION
Reconstition
– Route
Oral Rate of Administration
–Comments
– OTHER INFORMATION
Slowly hydrolysed to nicotinic acid inositol nicotinate.
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