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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
1978-2-18
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pubmed:abstractText |
Two trials of maprotiline (Ludiomil) were performed in general practice. In the first study depressed patients were given either 75 mg of maprotiline in a single dose or 25 mg three times daily. Assessments of the severity of depression and of side-effects were made initially and following 1, 2 and 4 weeks' treatment. At each assessment measurements of plasma levels of maprotiline were made. A second trial was performed in which some patients receiving 75 mg single dose of maprotiline had whole blood levels of maprotiline assayed. Steady-state levels of maprotiline were achieved after one week but these levels showed considerable individual variability. No clear correlation emerged between clinical response, side-effects and plasma or blood levels. Some of the factors which may be responsible are discussed.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
0300-0605
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
5 Suppl 4
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
101-11
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:590605-Adult,
pubmed-meshheading:590605-Amitriptyline,
pubmed-meshheading:590605-Anthracenes,
pubmed-meshheading:590605-Depression,
pubmed-meshheading:590605-Female,
pubmed-meshheading:590605-Humans,
pubmed-meshheading:590605-Male,
pubmed-meshheading:590605-Maprotiline,
pubmed-meshheading:590605-Middle Aged
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pubmed:year |
1977
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pubmed:articleTitle |
Efficacy, side-effects, plasma and blood levels of maprotiline (Ludiomil).
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pubmed:publicationType |
Journal Article
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