Letrozole
Letrozole
CLINICAL USE
Treatment of advanced prostate cancer and endometriosis
DOSE IN NORMAL RENAL FUNCTION
11.25 mg every 3 months (SC depot injection, prostate cancer only)Or 3.75 mg every 4 weeks Endometriosis: 3.75 mg every month or 11.25 mg every 3 months for maximum 6 months (not to be repeated)
PHARMACOKINETICS
Molecular weight                           :1269.5 %Protein binding                           :43–49 %Excreted unchanged in urine     : <5 (+ metabolites) Volume of distribution (L/kg)       :27 litreshalf-life – normal/ESRD (hrs)      :3/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 Monitor closely 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   :Unknown dialysability. 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 drugsNone known ADMINISTRATION
Reconstition
With diluent provided Route
IM, SC depot Rate of Administration
–Comments
– OTHER INFORMATION
Women on dialysis may be at greater risk of ovarian hyperstimulation, possibly because dialysis affects circulating leuprorelin concentration so endogenous gonadotrophins were still excreted. Alternatively, haemodialysis patients may have increased responsiveness to endogenous gonadotrophinsLeuprorelin acetate.
See how to identify renal failure stages according to GFR calculation
See how to diagnose irreversible renal disease
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