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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
4
|
| pubmed:dateCreated |
1992-12-2
|
| pubmed:abstractText |
In a four-week, open label study of major depression, 15 patients who had failed to respond to a trial of fluoxetine 20 mg/day of 8-12 weeks duration were then treated with fluoxetine 40 mg/day for one week and then, if tolerated, with either 60 or 80 mg/day. The mean HAM-D-17 and CGIS scores of these 15 patients decreased significantly at the end of 4 weeks on a higher dosage of fluoxetine (60 or 80 mg/day) with respect to the beginning of the four-week study. No significant side-effects were noted.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Aug
|
| pubmed:issn |
0165-0327
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
25
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
229-34
|
| pubmed:dateRevised |
2009-9-28
|
| pubmed:meshHeading |
pubmed-meshheading:1430659-Adolescent,
pubmed-meshheading:1430659-Adult,
pubmed-meshheading:1430659-Depressive Disorder,
pubmed-meshheading:1430659-Dose-Response Relationship, Drug,
pubmed-meshheading:1430659-Drug Administration Schedule,
pubmed-meshheading:1430659-Female,
pubmed-meshheading:1430659-Fluoxetine,
pubmed-meshheading:1430659-Humans,
pubmed-meshheading:1430659-Male,
pubmed-meshheading:1430659-Middle Aged
|
| pubmed:year |
1992
|
| pubmed:articleTitle |
High-dose fluoxetine in the treatment of depressed patients not responsive to a standard dose of fluoxetine.
|
| pubmed:affiliation |
Clinical Psychopharmacology Unit, Massachusetts General Hospital, Boston 02114.
|
| pubmed:publicationType |
Journal Article
|