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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
1998-8-6
|
pubmed:abstractText |
Examine the relationship between buprenorphine and norbuprenorphine plasma concentrations with subject-reported withdrawal symptomatology during buprenorphine dose induction, maintenance treatments (daily and alternate-day dosing) and withdrawal.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Apr
|
pubmed:issn |
0965-2140
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
93
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
549-59
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:9684393-Administration, Sublingual,
pubmed-meshheading:9684393-Buprenorphine,
pubmed-meshheading:9684393-Heroin Dependence,
pubmed-meshheading:9684393-Humans,
pubmed-meshheading:9684393-Male,
pubmed-meshheading:9684393-Narcotic Antagonists,
pubmed-meshheading:9684393-Substance Withdrawal Syndrome,
pubmed-meshheading:9684393-Time Factors
|
pubmed:year |
1998
|
pubmed:articleTitle |
Relationship of plasma buprenorphine and norbuprenorphine to withdrawal symptoms during dose induction, maintenance and withdrawal from sublingual buprenorphine.
|
pubmed:affiliation |
Division of Forensic Toxicology, Armed Forces Institute of Pathology, Washington, DC, USA.
|
pubmed:publicationType |
Journal Article,
Clinical Trial,
Randomized Controlled Trial,
Research Support, Non-U.S. Gov't
|