fluvoxamine maleate
fluvoxamine maleate
Pharmacologic class: Selective serotonin reuptake inhibitor (SSRI)
Therapeutic class: Antidepressant, antiobsessive agent
Pregnancy risk category C
Action
Selectively inhibits serotonin reuptake in neurons. This inhibition is thought to relieve depression and reduce behaviors related to obsessive-compulsive disorder (OCD).
Availability
Capsules (extended-release): 100 mg, 150 mg
Tablets: 25 mg, 50 mg, 100 mg
Indications and dosages
➣ OCD
Adults: Initially, 50 mg P.O. daily at bedtime; may increase by 50 mg q 4 to 7 days until desired effect occurs (not to exceed 300 mg/day). If daily dosage exceeds 100 mg, give in two equally divided doses; if doses aren't equal, give larger dose at bedtime. As needed, adjust dosage periodically to maintain lowest effective dosage that controls symptoms (immediate-release formulation)
Children ages 8 to 17: Initially, 25 mg at bedtime; may increase by 25 mg/day q 4 to 7 days until desired effect occurs (up to 200 mg/day for patients up to age 11 or up to 300 mg for adolescents). If daily dosage exceeds 50 mg, give in divided doses, with larger dose at bedtime (immediate-release formulation).
➣ OCD; social anxiety disorder
Adults: 100 mg P.O. once daily at bedtime; titrate in 50-mg increments weekly, to a maximum of 300 mg/day (extended-release formulation).
Dosage adjustment
• Hepatic impairment
• Elderly patients
Off-label uses
• Autism
• Anxiety disorders
Contraindications
• Hypersensitivity to drug or other SSRIs
• MAO inhibitor use within past 14 days
Precautions
Use cautiously in:
• cardiovascular disease, hepatic or renal impairment, mania, seizures, suicidal tendency
• elderly patients
• labor and delivery
• pregnant or breastfeeding patients.
Administration
• Give with or without food.
• Discontinue 5 weeks before MAO inhibitor therapy is set to begin.
Adverse reactions
CNS: dizziness, drowsiness, headache, insomnia, nervousness, anxiety, apathy, manic or psychotic reactions, depression, hypokinesia or hyperkinesia, tremor, suicide or suicidal ideation (especially in child or adolescent)
CV: hypertension, orthostatic hypotension, palpitations, tachycardia
EENT: sinusitis
GI: nausea, vomiting, diarrhea, constipation, dyspepsia, flatulence, dry mouth, dysphagia, anorexia
GU: decreased libido, sexual dysfunction, anorgasmia
Musculoskeletal: hypertonia, myoclonus, twitching
Respiratory: cough, dyspnea
Skin: diaphoresis
Other: abnormal taste, tooth disorder, dental caries, edema, weight gain or loss, chills, fever, flulike symptoms, yawning, hot flashes, allergic reactions, hypersensitivity reaction
Interactions
Drug-drug. Beta-adrenergic blockers (such as propranolol), carbamazepine, lithium, L-tryptophan, methadone, some benzodiazepines, theophylline, tolbutamide, warfarin: decreased fluvoxamine metabolism, increased effects
Clozapine: increased clozapine blood level and risk of toxicity
MAO inhibitors: serotonin syndrome
Tricyclic antidepressants: increased fluvoxamine blood level
Drug-tests. Hepatic enzyme levels: increased
Drug-behaviors. Smoking: decreased fluvoxamine efficacy
Patient monitoring
See Watch closely for signs and symptoms of depression and suicidal ideation (especially in child or adolescent).
• Assess patient's appetite. Report weight gain or loss.
• Monitor liver function test results.
• Monitor cardiovascular status, particularly blood pressure.
Patient teaching
• Instruct patient to swallow extended-release capsules whole and not to break, crush, or chew them.
See Instruct patient or caregiver (especially with child or adolescent patient) to recognize and immediately report signs of suicidal intent or expressions of suicidal ideation.
• Inform patient that drug may take several weeks to be fully effective.
• Recommend establishing effective bedtime routine to minimize insomnia.
• Instruct female patient to notify prescriber if she becomes or intends to become pregnant. Caution her not to breastfeed.
• Caution patient to avoid driving and other hazardous activities until he knows how drug affects concentration and alertness.
• As appropriate, review all other significant and life-threatening adverse reactions and interactions, especially those related to the drugs, tests, and behaviors mentioned above.