| Fluoxetine Hydrochloride | |||
| Prozac | |||
Management of major depressive disorder.
Efficacy in hospital settings not established.
Management of OCD.
Management of PMDD (previously late luteal phase dysphoric disorder).
Management of moderate to severe bulimia nervosa (at least 3 bulimic episodes per week for 6 months).
SSRIs usually are preferred drugs in management of bulimia because of more favorable adverse effect profile.
Also has been used for management of anorexia nervosa†.
Not recommended as the sole or primary treatment of anorexia nervosa†.
Management of panic disorder with or without agoraphobia.
Short-term treatment of acute depressive episodes (alone† or in combination with olanzapine) in patients with bipolar disorder (bipolar depression).
May cause manic reactions when used as monotherapy in some patients; should not be used without mood stabilizing agents (e.g., lithium).
Has been used for the short-term treatment of exogenous obesity†.
Has been used for the symptomatic management of cataplexy† in a limited number of patients with cataplexy and associated narcolepsy.
Has been used in the management of alcohol dependence†.
Studies of SSRIs have generally shown modest effects on alcohol consumption.
Administer conventional capsules, tablets, and solution orally once (in the morning) or twice daily (preferably in the morning and at noon) without regard to meals. If sedation occurs, the second dose may be administered at bedtime.
Administer delayed-release preparation once weekly without regard to meals.
Administer fixed-combination fluoxetine/olanzapine capsules (Symbyax®) once daily in the evening.
Available as fluoxetine hydrochloride; dosage is expressed in terms of fluoxetine.
Consider prolonged elimination half-life of fluoxetine and norfluoxetine when titrating dosage or discontinuing therapy. Several weeks may be required before full effect of dosage alterations is realized.
Children and adolescents ≥8 years of age: initially, 10 or 20 mg daily. If therapy is initiated at 10 mg daily, it can be increased after 1 week to 20 mg daily.
Manufacturer states that both the initial and target dose in lower weight children may be 10 mg daily.
An increase in dosage to 20 mg daily may be considered after several weeks in lower weight children if insufficient clinical improvement is observed.
Children and adolescents ≥7 years of age: initially, 10 mg daily.
In adolescents and higher weight children, the dosage should be increased to 20 mg daily after 2 weeks; additional dosage increases may be considered after several more weeks if insufficient clinical improvement is observed.
In lower weight children, dosage increases may be considered after several weeks if insufficient clinical improvement is observed.
Usual dosages: 20–60 mg daily for adolescents and higher weight children or 20–30 mg daily for lower weight children.
As conventional capsules, tablets, or solution: Initially, 20 mg once daily (in the morning). May initiate with lower dosage (e.g., 5 mg daily, 20 mg every 2–3 days). If no improvement is apparent after several weeks of therapy with 20 mg daily, an increase in dosage may be considered.
Usual dosage: 10–80 mg daily.
Delayed-release capsules: 90 mg once weekly, beginning 7 days after the last 20 mg daily dose as conventional capsules, tablets, or solution.
If a satisfactory response is not maintained, consider reestablishing daily dosage regimen with conventional capsules, tablets, or solution.
Optimum duration not established; may require several months of therapy or longer.
Initially, 20 mg once daily. If no improvement is apparent after several weeks, dosage may be increased.
Usual dosage: 20–60 mg daily.
20 mg once daily given continuously throughout the menstrual cycle or intermittently (i.e., only during the luteal phase, starting 14 days prior to the anticipated onset of menstruation and continuing through the first full day of menses).
If the intermittent dosing regimen is used, it should be repeated with each new menstrual cycle.
60 mg daily (in the morning); dosage may be decreased as necessary to minimize adverse effects. Alternatively, dosage may be titrated up to recommended initial dosage over several days.
40 mg daily in weight-restored patients.†
Initially, 10 mg daily. Increase dosage after 1 week to 20 mg daily. 10–60 mg is effective; 20 mg daily most frequently used. Dosages >60 mg daily not systematically evaluated.
20–60 mg daily in conjunction with a mood-stabilizing agent (e.g., lithium).†
Initially, 25 mg of fluoxetine and 6 mg of olanzapine once daily in the evening as a fixed-combination capsule (Symbyax® 6/25).
This dosage generally should be used as initial and maintenance therapy in patients with a predisposition to hypotensive reactions, patients with hepatic impairment, or those with factors that may slow metabolism of the drugs(s) (e.g., female gender, geriatric age, nonsmoking status); when indicated, dosage should be escalated with caution.
In other patients, increase dosages according to patient response and tolerance as indicated. In clinical trials, antidepressive efficacy was demonstrated at olanzapine dosages ranging from 6–12 mg daily and fluoxetine dosages ranging from 25–50 mg daily. Dosages exceeding 18 mg of olanzapine and 75 mg of fluoxetine not evaluated in clinical studies.
Although the manufacturer states that long-term efficacy (>8 weeks) not established, patients have received the fixed combination ≤24 weeks in clinical trials. If used for >8 weeks, periodically reassess need for continued therapy.
20 mg once or twice daily in conjunction with CNS stimulant therapy (e.g., dextroamphetamine, methylphenidate).†
60 mg daily has been used.†
Higher than average antidepressant SSRI dosage apparently is required for reduced alcohol intake; fluoxetine 40 mg daily is comparable to placebo in efficacy.†
Conventional capsules, tablets, or solution: Maximum 80 mg daily.
Reduce dose and/or frequency; some clinicians recommend a 50% reduction in initial dosage for patients with well-compensated cirrhosis.
Carefully individualize dosage in substantial hepatic impairment; adjust based on tolerance and therapeutic response.
Consider reduction in dosage and/or frequency particularly in severe renal impairment. Supplemental doses after hemodialysis not necessary.
Consider reducing dose and/or frequency.
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