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Nortriptyline: Difference between revisions

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{{MedTemplate
{{MedTemplate
| generic          = Nortriptyline
| generic          = Nortriptyline (hydrochloride)
| brand            = Pamelor
| brand            = Pamelor (US brand discontinued; generic widely available), Aventyl
| classes          = TCA, Antidepressant
| structure        =
| mechanism        = Norepinephrine reuptake inhibitor
| classes          = [[:Category:Tricyclic antidepressants|Tricyclic antidepressant (TCA, secondary amine)]], [[:Category:Antidepressants|Antidepressant]], [[:Category:Neuropathic pain medicines|Neuropathic pain medicine]], [[:Category:Migraine prophylactics|Migraine prophylactic]]
| uses              = <vote slug="major-depressive-disorder-use">Major depressive disorder (FDA)</vote>, <vote slug="neuropathic-pain-broad-use">Neuropathic pain, often first-line (off-label; diabetic peripheral neuropathy, postherpetic neuralgia)</vote>, <vote slug="migraine-prophylaxis-use">Migraine prophylaxis (off-label)</vote>, <vote slug="chronic-pain-syndromes-use">Chronic pain syndromes (off-label)</vote>, <vote slug="smoking-cessation-adjunct-use">Smoking cessation adjunct (off-label, modest evidence)</vote>
| starting_dose    = Depression: 25 mg PO TID-QID or 75 mg at bedtime, titrate to 75-150 mg/day. Neuropathic pain: 10-25 mg at bedtime, titrate to 50-100 mg/day. Elderly: 10 mg at bedtime (Beers-list cautions, though less than amitriptyline)
| preparations      = Capsules 10, 25, 50, 75 mg; oral solution 10 mg/5 mL
| fda_max          = 150 mg/day; therapeutic plasma-level monitoring recommended (target 50-150 ng/mL window)
| pill_id          =
| routes            = Oral
| onset            = Pain and migraine prophylaxis effect 1-4 weeks; antidepressant effect 4-6 weeks
| duration          = 24 hours (HS dosing)
| halflife          = 18-44 hours<ref name="pamelor-label">FDA Prescribing Information, Pamelor (nortriptyline hydrochloride), Mallinckrodt/various, current revision. https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/018012s029,018013s059lbl.pdf</ref>
| bioavailability  = ~50% (oral)<ref name="pamelor-label" />
| pregnancy        = TCA class signal; limited human data specific to nortriptyline.{{citation needed}}
| legal            = [[USLegal:Prescription only|Rx-only]] in US. Carries the antidepressant '''Boxed Warning''' for suicidality in children, adolescents, and young adults<ref name="pamelor-label" />
| mechanism        = <vote slug="nortriptyline-mech-claim">'''Secondary amine TCA''', the active metabolite of amitriptyline, with substantially less anticholinergic, antihistaminergic, and α1-adrenergic activity than the parent compound. This makes nortriptyline the "cleaner" TCA, generally preferred over amitriptyline in elderly patients and in chronic pain where the tertiary-amine side-effect burden is undesirable. Selective norepinephrine reuptake inhibition predominates over serotonin reuptake inhibition.</vote> Therapeutic plasma-level monitoring is standard practice for TCAs given the narrow therapeutic index and the established plasma-level-efficacy correlation. CYP2D6 substrate; CPIC PGx guidance applies for dose individualization<ref name="cpic-tca">CPIC Guideline for CYP2D6 and CYP2C19 Genotypes and Dosing of Tricyclic Antidepressants, 2016. https://cpicpgx.org/guidelines/guideline-for-tricyclic-antidepressants-and-cyp2d6-and-cyp2c19/</ref>.
}}
}}
== References ==
<references />
[[Category:Tricyclic antidepressants]]
[[Category:Antidepressants]]
[[Category:Antidepressants]]
 
[[Category:Neuropathic pain medicines]]
[[Category:Migraine prophylactics]]