Diferencia entre revisiones de «Doxepin»
(Created page with "==Administration== *Type: Insomnia; Tricyclic Antidepressants (TCAs) *Dosage Forms: 10, 25, 50, 75, 100, 150; 10/mL *Routes of Administration: PO *Common Trade Names: Silenor,...") |
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==Administration== | ==Administration== | ||
*Type: Insomnia; Tricyclic | *Type: Insomnia; [[Tricyclic antidepressant]] (TCAs) | ||
*Dosage Forms: 10, 25, 50, 75, 100, 150; 10/mL | *Dosage Forms: 10, 25, 50, 75, 100, 150; 10/mL | ||
*Routes of Administration: PO | *Routes of Administration: PO | ||
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==Adult Dosing== | ==Adult Dosing== | ||
Depression | ===[[Depression]]=== | ||
*150-300mg PO QHS | *150-300mg PO QHS | ||
*start 25-75mg PO QHS; max 300mg/day | *start 25-75mg PO QHS; max 300mg/day | ||
*taper gradually to | *taper gradually to discontinue | ||
Anxiety | ===[[Anxiety]]=== | ||
*150-300mg PO QHS | *150-300mg PO QHS | ||
*start 25-75mg PO QHS; max 300mg/day | *start 25-75mg PO QHS; max 300mg/day | ||
*taper gradually to | *taper gradually to discontinue | ||
Insomnia | ===[[Insomnia]]=== | ||
*10-50mg PO QHS | *10-50mg PO QHS | ||
==Pediatric Dosing== | ==Pediatric Dosing== | ||
===[[Depression]]=== | |||
*PO: | |||
* Not recommended as first line medication; however some studies indicate it might be beneficial for patients with comorbid conditions. | |||
*Children 7 to 11 years: Limited data available; efficacy results variable: 1 to 3 mg/kg/day in single or divided doses. | |||
*Children ≥12 years and Adolescents: Initial: 25 to 75 mg/day at bedtime or in 2 to 3 divided doses; begin at the low end of range and gradually titrate; select patients may respond to 25 to 50 mg/day; maximum single dose: 150 mg; maximum daily dose: 300 mg/day. | |||
** Note: Controlled clinical trials have not shown TCAs to be superior to placebo for the treatment of depression in children and adolescents | |||
==Special Populations== | ==Special Populations== | ||
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*Allergy to class/drug | *Allergy to class/drug | ||
*MI, acute recovery | *MI, acute recovery | ||
*glaucoma | *glaucoma, increased IOP | ||
*urinary retention, prostatic hypertrophy, GI/GU obstruction | |||
*urinary retention | |||
*avoid abrupt withdrawal | *avoid abrupt withdrawal | ||
*caution | *caution if: | ||
* | **age <25 years, elderly | ||
* | **cardiovascular disease | ||
* | **seizure disorder, parkinsons | ||
* | **thyroid disease, diabetes | ||
* | **asthma | ||
* | **hepatic impairment | ||
* | **schizophrenia, bipolar disorder, alcohol abuse, electroconvulsive therapy, suicide risk | ||
* | **high environmental temperature | ||
* | |||
* | |||
==Adverse Reactions== | ==Adverse Reactions== | ||
===Serious=== | ===Serious=== | ||
* | *syncope, orthostatic hypotension | ||
*ventricular arrhythmias, AV block, QT prolongation, torsades de pointes | |||
*seizures | |||
*ventricular arrhythmias | *MI, HTN | ||
* | |||
*MI | |||
*stroke | *stroke | ||
*extrapyramidal symptoms, tardive dyskinesia | |||
*extrapyramidal | |||
*ataxia | *ataxia | ||
*paralytic ileus | *paralytic ileus | ||
*IOP elevation | *IOP elevation | ||
*agranulocytosis | *agranulocytosis, leukopenia, thrombocytopenia | ||
*hallucinations, psychosis, worsening depression, hypomania/mania, suicidality | |||
*hallucinations | |||
*SIADH | *SIADH | ||
*hepatitis | *hepatitis | ||
*angioedema | *angioedema | ||
* | *hyperthermia, heat stroke | ||
*withdrawal symptoms if abruptly discontinued | |||
*withdrawal | |||
===Common=== | ===Common=== | ||
*drowsiness | *drowsiness, dizziness, confusion, weakness, tremor, paresthesias | ||
*nausea/vomiting, constipation, xerostomia | |||
*constipation | |||
*blurred vision | *blurred vision | ||
*palpitations | *palpitations, tachycardia, diaphoresis, restlessness, insomnia, anxiety | ||
*urinary frequency, incontinence, retention | |||
*increased appetite, weight gain | |||
*libido changes, impotence, gynecomastia, galactorrhea | |||
*urinary retention | |||
* | |||
*libido changes | |||
*hypo/hyperglycemia | *hypo/hyperglycemia | ||
* | *rash/urticarial, pruritus, photosensitivity | ||
==Pharmacology== | ==Pharmacology== | ||
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==References== | ==References== | ||
<references/> | <references/> | ||
[[Category:Pharmacology]] | [[Category:Pharmacology]] [[Category:Psychiatry]] | ||
Revisión actual - 18:18 22 sep 2019
Administration
- Type: Insomnia; Tricyclic antidepressant (TCAs)
- Dosage Forms: 10, 25, 50, 75, 100, 150; 10/mL
- Routes of Administration: PO
- Common Trade Names: Silenor, Zonalon, Prudoxin
Adult Dosing
Depression
- 150-300mg PO QHS
- start 25-75mg PO QHS; max 300mg/day
- taper gradually to discontinue
Anxiety
- 150-300mg PO QHS
- start 25-75mg PO QHS; max 300mg/day
- taper gradually to discontinue
Insomnia
- 10-50mg PO QHS
Pediatric Dosing
Depression
- PO:
- Not recommended as first line medication; however some studies indicate it might be beneficial for patients with comorbid conditions.
- Children 7 to 11 years: Limited data available; efficacy results variable: 1 to 3 mg/kg/day in single or divided doses.
- Children ≥12 years and Adolescents: Initial: 25 to 75 mg/day at bedtime or in 2 to 3 divided doses; begin at the low end of range and gradually titrate; select patients may respond to 25 to 50 mg/day; maximum single dose: 150 mg; maximum daily dose: 300 mg/day.
- Note: Controlled clinical trials have not shown TCAs to be superior to placebo for the treatment of depression in children and adolescents
Special Populations
- Pregnancy Rating: C
- Lactation risk: unsafe
Renal Dosing
- Adult: no adjustment
Hepatic Dosing
- Adult: not defined, caution advised
Contraindications
- Allergy to class/drug
- MI, acute recovery
- glaucoma, increased IOP
- urinary retention, prostatic hypertrophy, GI/GU obstruction
- avoid abrupt withdrawal
- caution if:
- age <25 years, elderly
- cardiovascular disease
- seizure disorder, parkinsons
- thyroid disease, diabetes
- asthma
- hepatic impairment
- schizophrenia, bipolar disorder, alcohol abuse, electroconvulsive therapy, suicide risk
- high environmental temperature
Adverse Reactions
Serious
- syncope, orthostatic hypotension
- ventricular arrhythmias, AV block, QT prolongation, torsades de pointes
- seizures
- MI, HTN
- stroke
- extrapyramidal symptoms, tardive dyskinesia
- ataxia
- paralytic ileus
- IOP elevation
- agranulocytosis, leukopenia, thrombocytopenia
- hallucinations, psychosis, worsening depression, hypomania/mania, suicidality
- SIADH
- hepatitis
- angioedema
- hyperthermia, heat stroke
- withdrawal symptoms if abruptly discontinued
Common
- drowsiness, dizziness, confusion, weakness, tremor, paresthesias
- nausea/vomiting, constipation, xerostomia
- blurred vision
- palpitations, tachycardia, diaphoresis, restlessness, insomnia, anxiety
- urinary frequency, incontinence, retention
- increased appetite, weight gain
- libido changes, impotence, gynecomastia, galactorrhea
- hypo/hyperglycemia
- rash/urticarial, pruritus, photosensitivity
Pharmacology
- Half-life: 15.3 hours (doxepin); 31 hours (metabolite)
- Metabolism: liver; CYP450 (1A2, 2C9/19, 2D6 substrate)
- Excretion: urine
- Mechanism of Action: exact MOA unknown; inhibits norepinephrine and serotonin reuptake; antagonizes central H1 receptors
