DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES
CAPD                :Unlikely to be dialysed. Dose as in GFR <10 mL/min
HD                     :Not dialysed. Dose as in GFR <10 mL/min
HDF/high flux   :Unknown dialysability. Dose as in GFR <10 mL/min
CAV/VVHD      :Unknown dialysability. Dose as for GFR=10–30 mL/min
IMPORTANT DRUG INTERACTIONS
Potentially hazardous interactions with other drugs
Analgesics: increased risk of bleeding with aspirin and NSAIDs; increased risk of CNS toxicity with tramadol
Anti-arrhythmics: possibly inhibits propafenone metabolism (increased risk of toxicity)
Anticoagulants: effect of coumarins possibly enhanced
Antidepressants: avoid concomitant use with MAOIs and moclobemide (increased risk of toxicity); avoid concomitant use with St John’s wort; possibly enhanced serotonergic effects with duloxetine; can increase tricyclics antidepressant concentration; increased agitation and nausea with tryptophan
Anti-epileptics: antagonism (lowered convulsive threshold); concentration reduced by carbamazepine, phenytoin and primidone
Antimalarials: avoid concomitant use with artemether/lumefantrine
Antipsychotics: concentration of clozapine, sertindole and possibly risperidone increased; metabolism of perphenazine inhibited, reduce dose of perphenazine; possibly inhibit aripiprazole metabolism, reduce aripiprazole dose
Antivirals: concentration increased by ritonavir
Dopaminergics: use entacapone with caution; increased risk of hypertension and CNS excitation with selegiline – avoid concomitant use; increased risk of CNS toxicity with rasagiline – avoid concomitant use5HT 1 agonist: risk of CNS toxicity increased by sumatriptan – avoid concomitant use; possibly increased risk of serotonergic effects with frovatriptan
Lithium: increased risk of CNS effects – monitor levels
Sibutramine: increased risk of CNS toxicity – avoid concomitant use