Nortrilen

Nortrilen

nortriptyline

Manufacturer:

Lundbeck

Distributor:

DKSH
/
Four Star
Concise Prescribing Info
Contents
Nortriptyline
Indications/Uses
Major depressions, especially when inhibition, apathy & lack of initiative are features of the illness. Depressive states in schizophrenics used in combination w/ a neuroleptic to prevent exacerbation of hallucinations & paranoid delusions.
Dosage/Direction for Use
Dosages exceeding 150 mg/day should preferably be restricted to hospitalised patients (up to 200-250 mg). Adult Initially 50 mg once daily in the morning or 25 mg bd-tds gradually increased, if necessary, by 25 mg every other day up to 100-150 mg once daily or 50 mg bd-tds. Elderly >60 yr Initially 10 mg bd-tds or 25 mg once daily, gradually increased, if necessary, every other day up to 150 mg daily. Reduced renal function Usual doses can be given. Reduced liver function Careful dosing &, if possible, a serum level determination is advisable. Dose increases are made preferably in the morning.
Administration
May be taken with or without food.
Contraindications
Hypersensitivity. Recent MI. Any degree of heart block, conduction disturbances affecting the heart rhythm & coronary artery insufficiency. Concomitant or recent treatment w/ MAOIs.
Special Precautions
Cardiac arrhythmias are likely to occur w/ high dosage. They may also occur in patients w/ pre-existing heart disease taking normal dosage. Nortriptyline should be used w/ caution in patients w/ convulsive disorders, urinary retention, prostatic hypertrophy, hyperthyroidism, paranoid symptomatology, & advanced hepatic or CV disease. Serotonergic psychiatric drugs should not be started in a patient receiving linezolid, wait until 24 hr after the last dose of linezolid. Depression is associated w/ an increased risk of suicidal thoughts, self-harm & suicide (suicide-related events). The risk of suicide may increase in the early stages of recovery. Close supervision of patients & in particular those at high risk should accompany drug therapy especially in early treatment & following dose changes. Patients (& caregivers of patients) should be alerted about the need to monitor for any clinical worsening, suicidal behaviour or thoughts & unusual changes in behaviour & to seek medical advice immediately if these symptoms present. Great care is necessary if nortriptyline is administered to hyperthyroid patients or to those receiving thyroid medication, since cardiac arrhythmias may develop. In manic-depressives, a shift towards the manic phase may occur; should the patient enter a manic phase nortriptyline should be discontinued. Nortriptyline should be used in combination w/ a neuroleptic. In patients w/ the rare condition of shallow anterior chamber & narrow chamber angle, attacks of acute glaucoma due to dilation of the pupil may be provoked. Anaesth given during tri/tetracyclic antidepressant therapy may increase the risk of arrhythmias & hypotension. If possible, discontinue nortriptyline several days before surgery; if emergency surgery is unavoidable, the anaesthetist should be informed that the patient is being so treated. Nortriptyline may modify insulin & glucose responses calling for adjustment of the antidiabetic therapy in diabetic patients; in addition the depressive illness itself may affect patients' glucose balance. Hyperpyrexia has been reported w/ TCAs when administered w/ anticholinergic or w/ neuroleptic medications, especially in hot weather. After prolonged administration, abrupt cessation of therapy may produce w/drawal symptoms eg, headache, malaise, insomnia & irritability. Treatment w/ Nortrilen is associated w/ a risk of CV adverse events in all age groups. The tablets contain lactose monohydrate. Should not be administered during pregnancy unless the expected benefit to the patient outweighs the theoretical risk to the foetus. Breast-feeding can be continued during nortriptyline therapy if considered of clinical importance, but observation of the infant is recommended. When stopping therapy, the drug should be gradually w/drawn during several wk. Not recommended in childn & adolescents <18 yr.
Adverse Reactions
Tremor, dizziness, headache, sedation (drowsiness, urge to sleep); accommodation disorder; palpitations, tachycardia; dry mouth, constipation, nausea; hyperhidrosis; increased wt. Confusional state, libido decreased; disturbance in attention, dysgeusia, paresthesia, ataxia; mydriasis; AV block, bundle branch block; orthostatic hypotension; erectile dysfunction; fatigue; ECG abnormal, ECG QT prolonged, ECG QRS complex prolonged.
Drug Interactions
Combination w/ MAOIs is contraindicated (risk of serotonin syndrome). Inadvisable combinations: Sympathomimetic agents, adrenergic neurone blockers, anticholinergic agents, drugs which prolong the QT-interval, antifungals. Caution is advised when used w/ CNS depressants. Neuroleptics, serotonin reuptake inhibitors except citalopram, β-blockers, & newer antiarrhythmics may produce marked increases in plasma conc. Barbiturates & other enzyme inducers may lower plasma levels of TCAs & reduce antidepressant response. Cimetidine, methylphenidate & Ca-channel blockers increase plasma levels of tricyclics & accompanying toxicity. TCAs & neuroleptics may lead to a lowered convulsion threshold, & seizures. Antifungals eg, fluconazole & terbinafine have been observed to increase serum levels of amitriptyline & nortriptyline. Nortriptyline plasma conc can be increased by valproic acid. Clinical monitoring is therefore recommended.
MIMS Class
Antidepressants
ATC Classification
N06AA10 - nortriptyline ; Belongs to the class of non-selective monoamine reuptake inhibitors. Used in the management of depression.
Presentation/Packing
Form
Nortrilen tab 10 mg
Packing/Price
100's
Form
Nortrilen tab 25 mg
Packing/Price
100's
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