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| {{Drugbox|
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| | IUPAC_name = 3-(10,11-dihydro-5H-dibenzo[a,d] cyclohepten-5-ylidene)- N-methyl-1-propanamine
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| | image=Nortriptyline.png
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| | width =120
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| | CAS_number = 72-69-5
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| | CAS_supplemental = 894-71-3 (hydrochloride)
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| | ATC_prefix=N06
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| | ATC_suffix=AA10
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| | PubChem=4543
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| | DrugBank=APRD00602
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| | C=19 | H=21 | N=1
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| | molecular_weight = 263.377 g/mol
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| | bioavailability = well absorbed
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| | metabolism = [[Hepatic]]
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| | elimination_half-life = 16 and 90 hours
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| | excretion = [[Renal]]
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| | pregnancy_AU =
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| | pregnancy_US =
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| | pregnancy_category = C
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| | legal_status = Rx-only
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| | routes_of_administration = oral
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| }}
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| '''Nortriptyline''' is a second generation [[tricyclic antidepressant]] marketed as the [[hydrochloride]] under the trade names '''Aventyl'''®, '''Pamelor'''® and '''Nortrilen'''®. It is used in the treatment of [[clinical depression|depression]] and childhood [[nocturnal enuresis]] (bedwetting). In addition it is sometimes used for [[chronic pain]] modification, [[Migraine]], and [[labile affect]] in some neurological conditions.
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| ==Clinical pharmacology==
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| Nortriptyline inhibits the reuptake of [[serotonin]], and, to a lesser extent, [[norepinephrine]] (noradrenalin) (''Basic & Clinical Pharmacology, 10th Edition'', Bertram G. Katzung, MD, PhD). Operant conditioning techniques in rats and pigeons suggest that nortriptyline has a combination of stimulant and depressant properties.
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| ==Indications==
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| FDA-approved for treatment of depressive disorders. In the [[United Kingdom]] also may be used for treating nocturnal enuresis with courses of treatment lasting no more than three months. Also used [[off-label use|off-label]] for the treatment of [[panic disorder]], [[irritable bowel syndrome|irritable bowel disease]], prevention of [[migraine]] headaches and chronic pain or [[neuralgia]] modification (particularly [[Temporomandibular joint disorder]]).<ref name="Martindale2002-Sweetman">{{cite book | editor = Sweetman SC | title =Martindale. The complete drug reference | edition = 33 | year = 2002 | publisher = Pharmaceutical Press | id = ISBN 0-85369-499-0}}</ref> It can also aid in quitting smoking with one study showing a six-month abstinence rate of 14% for subjects receiving nortriptyline compared to 3% for subjects not undergoing pharmacological treatment.<ref name="Arch Intern Med1998-prochazka">{{cite journal | author = Prochazka A, Weaver M, Keller R, Fryer G, Licari P, Lofaso D | title = A randomized trial of nortriptyline for smoking cessation. | journal = Arch Intern Med | volume = 158 | issue = 18 | pages = 2035-9 | year = 1998 | id = PMID 9778204}}</ref>
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| ==Metabolism==
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| Nortriptyline is metabolised in the liver by [[hepatic enzyme]] [[CYP2D6]]. Approximately 7 to 10 percent of [[Caucasian race|Caucasians]] are poor metabolisers and might experience more adverse effects, so a lower dosage is often necessary in these individuals.{{Fact|date=February 2007}} Blood levels of nortriptyline should be obtained during long term treatment to avoid toxicity and optimise response.
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| ==Dosage==
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| For depression: low starting doses are used, increasing as necessary to 75–100mg (0–50mg for adolescents and the elderly). Maximum daily dosage is 150mg.<ref name="BNF">[[British National Formulary]] '''45''' March 2003</ref>
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| For the management of noctiral enuresis: lower dosages are used with the maximum period of treatment, including gradual withdrawal, being three months and a full examination including [[electrocardiogram]] (ECG or EKG) required before further courses.<ref name="BNF"/>
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| For its off-label use for migraine and headache prophylaxis and treating chronic pain: treatment is started at very low 10mg once at night to minimise side-effects. The dose is then increased every two weeks if required to a maximum of 150mg.
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| ==Side effects==
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| Dry mouth, drowsiness, [[orthostatic hypotension]], [[urinary retention]], [[constipation]], and rapid or [[irregular heartbeat]]. Some sexual side effects may be a problem as well. Less commonly, [[seizures]] and ECG/EKG changes have been reported, especially in [[overdose]].
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| Alcohol may exacerbate some of its side effects and should be avoided.
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| However, the incidence of side effects with nortriptyline is somewhat lower than with the first generation tricyclics (e.g. [[imipramine]] (Tofranil®), [[amitriptyline]] (Elavil®)).
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| ==Warnings==
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| Closer monitoring is required for those with a history of cardiovascular disease, [[stroke]], [[glaucoma]] and/or [[seizures]] as well as those who have [[hyperthyroidism]] or are receiving thyroid medication.
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| ==Contraindications==
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| In the acute recovery phase after [[myocardial infarction]] (e.g. heart attack). As for all tricyclic antidepressants concurrent use, or failure to allow a two week gap, with [[monoamine oxidase inhibitor]]s (MAO inhibitors, e.g. phenelzine, tranylcypromine, etc.) may precipitate [[hyperthermia|hyperpyretic]] crises and/or severe [[convulsions]]; fatalities have occurred.
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| ==Overdose==
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| {{main|Tricyclic antidepressant}}
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| The symptoms and the treatment of an overdose are largely the same as for the other tricyclic antidepressants.
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| ==Footnotes==
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| <div class="references-small">
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| {{reflist|2}}
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| </div>
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| {{Antidepressants}}
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| [[Category:Tricyclic antidepressants]]
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| [[nl:Nortriptyline]]
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