saquinavir
CLINICAL USE
Protease inhibitor:Treatment of HIV infection in combination with other antiviral drugs
DOSE IN NORMAL RENAL FUNCTION
With low dose ritonavir: 1 g twice daily
PHARMACOKINETICS
Molecular weight                           :670.8 %Protein binding                           :98 %Excreted unchanged in urine     : <4 Volume of distribution (L/kg)       :10half-life – normal/ESRD (hrs)      :13.2 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                :Unlikely to be dialysed. Dose as in normal renal function HD                     :Unlikely to be dialysed. Dose as in normal renal functionHDF/high flux   :Not dialysed. Dose as in normal renal functionCAV/VVHD      :Unknown dialysability. Dose as in normal renal function IMPORTANT DRUG INTERACTIONS
Potentially hazardous interactions with other drugsAntibacterials: rifampicin and rifabutin can reduce saquinavir levels by 80% and 40% respectively (metabolism accelerated); increased hepatoxicity with rifampicin; concentration possibly increased by quinupristin/dalfopristin; avoid with telithromycin in severe renal and hepatic failureAntidepressants: concentration reduced by St John’s wort – avoidAnti-epileptics: carbamazepine, phenobarbital, primidone and phenytoin can reduce saquinavir levelsAntimalarials: avoid concomitant use with artemether/lumefantrineAntipsychotics: possibly increased risk of ventricular arrhythmias with pimozide and sertindole – avoid concomitant use; possibly inhibits aripiprazole metabolism – reduce aripiprazole doseAntivirals: tipranavir and efavirenz can reduce saquinavir levels; nelfinavir can cause an increase in levels of both nelfinavir and saquinavir; concentration increased by atazanavir, indinavir, lopinavir and ritonavir; reduced darunavir concentration
Anxiolytics and hypnotics: midazolam plasma concentration possibly increased (prolonged sedation) – avoidCiclosporin: concentration of both drugs increasedCilostazol: concentration of cilostazol possibly increased – avoid concomitant use Ergot alkaloids: risk of ergotism – avoid Lipid-lowering drugs: increased risk of myopathy with simvastatin – avoid; possibly increased myopathy with atorvastatin
Omeprazole: AUC of saquinavir increased by 82% (increased risk of toxicity) Tacrolimus: possibly increased tacrolimus concentration – may need to reduce dose ADMINISTRATION
Reconstition
– Route
Oral Rate of Administration
–Comments
Administer within 2 hours after meal OTHER INFORMATION
See how to identify renal failure stages according to GFR calculation
See how to diagnose irreversible renal disease
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