Zolpidem tartrate
CLINICAL USE
Insomnia (short-term treatment)
DOSE IN NORMAL RENAL FUNCTION
5–10 mg at night
PHARMACOKINETICS
Molecular weight                           : 764.9 %Protein binding                           : 92.5 %Excreted unchanged in urine     : Negligible (56% as active metabolites) Volume of distribution (L/kg)       : 0.34–0.54 (depends on age) half-life – normal/ESRD (hrs)      : Average: 2.4/ Increased DOSE IN RENAL IMPAIRMENT
GFR (mL/MIN)
20 to 50     : Dose as in normal renal function 10 to 20     : Dose as in normal renal function <10           : Dose as in normal renal function DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES
CAPD                : Not dialysed. Dose as in normal renal function HD                     : Not dialysed. Dose as in normal renal function HDF/high flux   : Unknown dialysability. Dose as in normal renal function CAV/VVHD      : Not dialysed. Dose as in normal renal function IMPORTANT DRUG INTERACTIONS
Potentially hazardous interactions with other drugs Antibacterials: metabolism accelerated by rifampicin Antipsychotics: enhanced sedative effects Antivirals: concentration increased by ritonavir (risk of extreme sedation and respiratory depression) – avoid concomitant use ADMINISTRATION
Reconstition
– Route
Oral Rate of Administration
– Comments
– OTHER INFORMATION
First pass metabolism by liver is 35% Clearance is reduced in renal impairment .
See how to identify renal failure stages according to GFR calculation
See how to diagnose irreversible renal disease
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