Abstract | BACKGROUND: AIMS: METHOD: Patients with panic disorder were randomised to placebo or to fluoxetine initiated at 10 mg daily for 1 week and then increased to 20 mg daily. The trial lasted 12 weeks, but after 6 weeks patients who had failed to achieve a satisfactory response were eligible for dose escalation to a maximum of 60 mg of fluoxetine daily. RESULTS:
Fluoxetine was associated with a statistically significantly greater proportion of panic-free patients compared with placebo after 6 weeks and at end-point. CONCLUSIONS:
Fluoxetine at a dose of 20 mg daily is safe and efficacious in reducing symptoms of panic disorder. Patients who fail to obtain a satisfactory response at 20 mg daily may benefit from further dose increases.
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Authors | D Michelson, C Allgulander, K Dantendorfer, A Knezevic, D Maierhofer, V Micev, V R Paunovic, I Timotijevic, N Sarkar, L Skoglund, S C Pemberton |
Journal | The British journal of psychiatry : the journal of mental science
(Br J Psychiatry)
Vol. 179
Pg. 514-8
(Dec 2001)
ISSN: 0007-1250 [Print] England |
PMID | 11731354
(Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antidepressive Agents, Second-Generation
- Serotonin Uptake Inhibitors
- Fluoxetine
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Topics |
- Adult
- Antidepressive Agents, Second-Generation
(administration & dosage, adverse effects)
- Double-Blind Method
- Drug Administration Schedule
- Female
- Fluoxetine
(administration & dosage, adverse effects)
- Humans
- Male
- Middle Aged
- Panic Disorder
(drug therapy)
- Psychiatric Status Rating Scales
- Selective Serotonin Reuptake Inhibitors
(administration & dosage, adverse effects)
- Single-Blind Method
- Treatment Outcome
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