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| (DOX-uh-pin HIGH-droe-KLOR-ide) |
Sinequan, Zonalon, Alti-Doxepin, Apo-Doxepin, Novo-Doxepin, Rho-Doxepin, Triadapin |
| Class: Antianxiety/Tricyclic antidepressant |
Action Moderately blocks reuptake of norepinephrine and weakly blocks reuptake of serotonin; also produces antihistaminic and anticholinergic activity.
Indications Treatment of psychoneurotic patients with depression or anxiety; depression or anxiety associated with alcoholism (not to be taken concomitantly with alcohol); depression or anxiety associated with organic disease (the possibility of drug interaction should be considered if the patient is receiving other drugs concomitantly); psychotic depressive orders with associated anxiety including involutional depression and manic-depressive disorders. Unlabeled use(s): Neurogenic pain; peptic ulcer disease. Topical use: Pruritus.
Contraindications Hypersensitivity to tricyclic antidepressants; use during acute recovery phase after MI; angle-closure glaucoma; risk of urinary retention; concomitant use with monoamine oxidase (MAO) inhibitor; Dibenzoxepines may produce cross-sensitivity.
Depression
ADULTS: PO Initial dose: 75 mg/day, increasing as tolerated. Maximum daily dose: 150 mg for outpatients, 300 mg for inpatients. Maximum single daily dose: 150 mg given at bedtime. FOR MILD CASES WITH ORGANIC DISEASES: PO 25 to 50 mg/day.
Pruritus
ADULTS: Topical Apply thin film qid with ³ 3 to 4 hr between applications. Not recommended for > 8 days.
Alcohol/CNS depressants: CNS and respiratory depression may be potentiated. Anticoagulants: Anticoagulant action may increase. Cimetidine: May inhibit metabolism of doxepin, leading to increased concentrations. Clonidine: Concurrent use may lead to dangerous increases in BP. Fluoxetine: May increase serum concentrations of doxepin; effect may occur up to 5 wk after discontinuation of fluoxetine. Guanethidine: Hypotensive action may be inhibited. MAO inhibitors: Concurrent use may lead to severe seizures, hyperpyretic crisis and fatal reactions. Generally, allow 7 to 10 days between discontinuation of one drug and start of other. Sympathomimetics (eg, dopamine, epinephrine): Pressor response may increase or decrease; arrhythmias may occur.
Lab Test Interferences None well documented.
CV: Orthostatic hypotension; hypertension; fainting; tachycardia; arrhythmias; MI; heart block, precipitation of CHF; stroke. CNS: Dizziness; drowsiness; headache; confusion; weakness; tremors; convulsions. EENT: Mydriasis; photophobia; blurred vision; increased IOP; unpleasant taste. GI: Nausea; constipation; dry mouth; paralytic ileus. GU: Urinary retention; nocturia; painful ejaculation; altered libido; impotence; dysmenorrhea. HEPA: Hepatitis. HEMA: Agranulocytosis; eosinophilia; purpura; thrombocytopenia; leukopenia. META: Increased appetite; weight gain; syndrome of inappropriate secretion of antidiuretic hormone. RESP Bronchospasms; dyspnea. OTHER: Hyperthermia. Topical use: Local burning or stinging; dry or tight skin. Results in significant plasma levels; drowsiness and other adverse effects are possible.
Pregnancy: Oral form: Safety not established. Lactation: Excreted in breast milk. Children: Not recommended for children < 12 yr. Special risk patients: Use drug with caution in patients with history of seizures, urinary retention, urethral spasm, angle-closure glaucoma or increased IOP, cardiovascular disorders, hyperthyroidism (or those receiving thyroid medication), hepatic or renal impairment, schizophrenia or paranoia. Topical use: For external use only; do not use ophthalmically, orally or intravaginally. Because of absorption of drug, drowsiness often occurs.
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