Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/54043
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dc.contributor.authorMcHenry, L.-
dc.contributor.authorJureidini, J.-
dc.date.issued2008-
dc.identifier.citationAccountability in research, 2008; 15(3):152-167-
dc.identifier.issn0898-9621-
dc.identifier.issn1545-5815-
dc.identifier.urihttp://hdl.handle.net/2440/54043-
dc.description.abstractIn this case study from litigation, we show how ghostwriting of clinical trial results can contribute to the manipulation of data to favor the study medication. Study 329 for paroxetine pediatric use was negative for efficacy and positive for harm. Yet the ghostwritten publication from this study concluded that paroxetine provided evidence of efficacy and safety and continues to be influential. Despite the role of named authors in revisions of the manuscript, the sponsor company remained in control of the message.-
dc.description.statementofresponsibilityLeemon B. McHenry and Jon N. Jureidini-
dc.language.isoen-
dc.publisherTaylor & Francis Inc.-
dc.source.urihttp://dx.doi.org/10.1080/08989620802194384-
dc.subjectCentral Medical Affairs Team-
dc.subjectclinical trials-
dc.subjectconflict of interest-
dc.subjectfinal clinical report-
dc.subjectGlaxoSmithKline-
dc.subjectindustry-sponsored ghostwriting-
dc.subjectkey opinion leader-
dc.subjectoff-label prescriptions-
dc.subjectparoxetine (Paxil-
dc.subjectSeroxat)-
dc.subjectPaxil Team-
dc.subjectprimary efficacy variables-
dc.subjectsecondary efficacy variables-
dc.subjectScientific Therapeutics Information-
dc.subjectserious adverse events-
dc.subjectSmithKline Beecham-
dc.titleIndustry-sponsored ghostwriting in clinical trial reporting: A case study-
dc.typeJournal article-
dc.identifier.doi10.1080/08989620802194384-
pubs.publication-statusPublished-
dc.identifier.orcidJureidini, J. [0000-0001-7585-2660]-
Appears in Collections:Aurora harvest
Psychiatry publications

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