Trade Names:Asendin- Tablets 25 mg- Tablets 50 mg- Tablets 100 mg- Tablets 150 mg
Inhibits reuptake of norepinephrine and serotonin in CNS.
Rapidly absorbed; t max is about 90 min.
About 90% protein bound.
Extensively metabolized. Major metabolite is 8-hydroxyamoxapine.
The t ½ is 8 h. Biologic t ½ of 8-hydroxyamoxapine is 30 h. Metabolites excreted in urine in conjugated form as glucuronides.
Relief of symptoms of depression.
Management of chronic pain associated with migraine, chronic tension headache, diabetic neuropathy, phantom limb pain, tic douloureux, cancer pain, peripheral neuropathy, postherpetic neuralgia, and arthritic pain.
Hypersensitivity to tricyclic antidepressants; not recommended for use during acute recovery phase of MI. Do not use drug concomitantly with MAOIs except under close medical supervision.
PO Initial dose: 200 to 300 mg/day; may be given in single daily dose at bedtime once effective dosage is established. Divided doses are given for amounts more than 300 mg/day. Hospitalized patients refractory to antidepressant therapy and with no history of seizures may be cautiously titrated to 600 mg/day in divided doses.Maintenance
Single daily dose of 300 mg or less at bedtime.Elderly
PO Initially 25 mg twice daily or 3 times daily. If well tolerated, may be increased to 50 mg twice daily or 3 times daily. Some patients may need up to 300 mg/day.
Store at room temperature in tightly closed container.
May decrease amoxapine blood levels.Cimetidine, fluoxetine
May increase amoxapine blood levels.Clonidine
May result in hypertensive crisis.CNS depressants
Depressant effects may be additive.MAOIs
May cause serious and possibly fatal hypertensive crisis.
None well documented.
Orthostatic hypotension; hypertension; tachycardia; palpitations; arrhythmias; ECG changes.
Confusion; hallucinations; delusions; nervousness; restlessness; disturbed concentration; decreased memory; agitation; panic; insomnia; nightmares; mania; exacerbation of psychosis; drowsiness; dizziness; weakness; emotional liability; seizures.
Rash; pruritus; photosensitivity reaction; dry skin; acne; itching.
Conjunctivitis; blurred vision; increased intraocular pressure; mydriasis; tinnitus; nasal congestion; peculiar taste in mouth.
Nausea; vomiting; anorexia; GI distress; diarrhea; flatulence; dry mouth; constipation.
Impotence; sexual dysfunction; nocturia; urinary frequency, retention or hesitancy; urinary tract infection; vaginitis; cystitis.
Bone marrow depression including agranulocytosis; eosinophilia; purpura; thrombocytopenia; leukopenia.
Elevation or depression of blood glucose levels.
Pharyngitis; rhinitis; sinusitis, cough.
Numbness; tremors; menstrual irregularities, dysmenorrhea; breast enlargement in men and women; extrapyramidal symptoms (pseudoparkinsonism, movement disorders, akathisia); tardive dyskinesia. Effects can generally be minimized by starting with low doses and increasing gradually.
Category C .
Excreted in breast milk.
Not recommended in children younger than 16 yr of age.
Use with caution in patients with history of seizures, urinary retention, urethral or ureteral spasm, angle-closure glaucoma or increased intraocular pressure, CV disorders, hyperthyroid patients or those patients receiving thyroid medication, hepatic or renal function impairment, schizophrenia, or paranoia.
Potentially fatal condition that has been reported with amoxapine. Signs and symptoms include hyperpyrexia, muscle rigidity, altered mental status, irregular pulse, irregular BP, tachycardia, and diaphoresis. Notify health care provider. Discontinue amoxapine and nonessential drugs.
Wait 7 to 10 days to prevent hypertensive crisis.
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