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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
1990-8-17
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pubmed:abstractText |
Dilevalol, 200 mg, was administered orally as seven daily doses to three groups of six participants, with differing degrees of renal impairment. Values of Cmax, Tmax, half-life or renal elimination did not significantly change with decreased renal function. Values of area under the plasma concentration-time curves and pre-dose concentrations tended to increase with renal impairment and there was a significant, if small, correlation between these and glomerular filtration rate. The practical clinical consequences of these results is that impairment is not likely to be associated with significant accumulation of dilevalol.
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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:month |
Jun
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pubmed:issn |
0950-9240
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
4 Suppl 2
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
59-62
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:2370645-Administration, Oral,
pubmed-meshheading:2370645-Adult,
pubmed-meshheading:2370645-Aged,
pubmed-meshheading:2370645-Female,
pubmed-meshheading:2370645-Glomerular Filtration Rate,
pubmed-meshheading:2370645-Half-Life,
pubmed-meshheading:2370645-Humans,
pubmed-meshheading:2370645-Hypertension,
pubmed-meshheading:2370645-Kidney Failure, Chronic,
pubmed-meshheading:2370645-Labetalol,
pubmed-meshheading:2370645-Male,
pubmed-meshheading:2370645-Middle Aged,
pubmed-meshheading:2370645-Reference Values
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pubmed:year |
1990
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pubmed:articleTitle |
The pharmacokinetics of dilevalol in renal impairment.
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pubmed:affiliation |
Institute of Biopharmaceuticals, Athlone, Ireland.
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pubmed:publicationType |
Journal Article
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