Local view for "https://dbmi-icode-01.dbmi.pitt.edu/dikb/resource/Evidence/1044"
Predicate | Value (sorted: default) |
rdfs:label |
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rdf:type |
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?:Evidence_assump_list_id |
"185"
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?:Evidence_enzyme_system |
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?:Evidence_type |
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?:claim_assumed_valid_for_evidence_application_evidence_1570 |
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?:content |
"Drugs Metabolized by Cytochrome P450IID6 (CYP2D6): Many drugs, including most antidepressants (SSRIs, many tricyclics), beta-blockers, antiarrhythmics, and antipsychotics are metabolized by the CYP2D6 isoenzyme. Although bupropion is not metabolized by this isoenzyme, bupropion and hydroxybupropion are inhibitors of the CYP2D6 isoenzyme in vitro. In a study of 15 male subjects (ages 19 to 35 years) who were extensive metabolizers of the CYP2D6 isoenzyme, daily doses of bupropion given as 150mg twice daily followed by a single dose of 50mg desipramine increased the Cmax, AUC, and t1/2 of desipramine by an average of approximately 2-, 5- and 2-fold, respectively. The effect was present for at least 7 days after the last dose of bupropion. Concomitant use of bupropion with other drugs metabolized by CYP2D6 has not been formally studied."
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dc:creator |
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dc:date |
"05/15/2009 10:51:26"
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rdfs:seeAlso |
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All properties reside in the graph file:///home/swish/src/ClioPatria/guidelines/dikb.ttl
The resource appears as object in one triple:
{ bupropion_inhibits_cyp2d6, <http://purl.org/swan/1.2/swan-commons#citesAsSupportingEvidence>, evidence_1570 }
Context graph