nortriptyline
CLINICAL USE
Tricyclic antidepressant
DOSE IN NORMAL RENAL FUNCTION
30–150 mg daily in single or divided doses
PHARMACOKINETICS
Molecular weight                           :263.4 (299.8 as hydrochloride) %Protein binding                           :95 %Excreted unchanged in urine     : <5 Volume of distribution (L/kg)       :15–23half-life – normal/ESRD (hrs)      :25–38/15–66 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. Start with small dose DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES
CAPD                :Not dialysed. Dose as in GFR <10 mL/min HD                     :Not dialysed. Dose as in GFR <10 mL/minHDF/high flux   :Unknown dialysability. Dose as in GFR <10 mL/minCAV/VVHD      :Not dialysed. Dose as in normal renal function IMPORTANT DRUG INTERACTIONS
Potentially hazardous interactions with other drugsAlcohol: increased sedative effect Analgesics: increased risk of CNS toxicity with tramadol; possibly increased risk of side effects with nefopam; possibly increased sedative effects with opioidsAnti-arrhythmics: increased risk of ventricular arrhythmias with amiodarone – avoid concomitant use; increased risk of ventricular arrhythmias with drugs that prolong the QT interval; increased risk of arrhythmias with propafenoneAntibacterials: increased risk of ventricular arrhythmias with moxifloxacin – avoid concomitant use; concentration reduced by rifampicinAnticoagulants: may alter anticoagulant effect of coumarinsAntidepressants: enhanced CNS excitation and hypertension with MAOIs and moclobemide – avoid concomitant use; concentration possibly increased with SSRIsAnti-epileptics: convulsive threshold lowered; concentration reduced by carbamazepine, primidone, barbiturates and possibly phenytoinAntimalarials: avoid concomitant use with artemether/lumefantrineAntipsychotics: increased risk of ventricular arrhythmias especially with pimozide; increased antimuscarinic effects with clozapine and phenothiazines; concentration increased by antipsychoticsAntivirals: increased TAD side effects with amprenavir; concentration possibly increased with ritonavirAtomoxetine: increased risk of ventricular arrhythmias and possibly convulsionsBeta-blockers: increased risk of ventricular arrhythmias with sotalolClonidine: tricyclics antagonise hypotensive effect; increased risk of hypertension on clonidine withdrawalDopaminergics: avoid use with entacapone; CNS toxicity reported with selegiline and rasagiline Pentamidine: increased risk of ventricular arrhythmiasSibutramine: increased risk of CNS toxicity – avoid concomitant useSympathomimetics: increased risk of hypertension and arrhythmias with adrenaline and noradrenaline; metabolism possibly inhibited by methylphenidate ADMINISTRATION
Reconstition
– Route
Oral Rate of Administration
–Comments
– OTHER INFORMATION
All metabolites are highly lipophilic .
See how to identify renal failure stages according to GFR calculation
See how to diagnose irreversible renal disease
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