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rdf:type |
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lifeskim:mentions |
|
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pubmed:issue |
11
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pubmed:dateCreated |
2010-10-20
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pubmed:abstractText |
To develop recommendations on monitoring for adverse events (AEs) of low-dose glucocorticoid (GC) therapy (?7.5 mg prednisone or equivalent daily) in clinical trials and daily practice.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
1468-2060
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pubmed:author |
pubmed-author:AndrewsTT,
pubmed-author:BijlsmaJ W JJW,
pubmed-author:Blom-BakkersM A MMA,
pubmed-author:BoeroAA,
pubmed-author:ButtgereitFF,
pubmed-author:CaeyersNN,
pubmed-author:CutoloMM,
pubmed-author:Da SilvaJ A PJA,
pubmed-author:GuillevinLL,
pubmed-author:JacobsJ W GJW,
pubmed-author:KirwanJ RJR,
pubmed-author:RovenskyJJ,
pubmed-author:SeverijnsGG,
pubmed-author:WebberSS,
pubmed-author:WesthovensRR,
pubmed-author:van der GoesM CMC
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pubmed:issnType |
Electronic
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pubmed:volume |
69
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pubmed:owner |
NLM
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|
pubmed:authorsComplete |
Y
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|
pubmed:pagination |
1913-9
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pubmed:meshHeading |
|
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pubmed:year |
2010
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pubmed:articleTitle |
Monitoring adverse events of low-dose glucocorticoid therapy: EULAR recommendations for clinical trials and daily practice.
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pubmed:affiliation |
Department of Rheumatology and Clinical Immunology, University Medical Center Utrecht, The Netherlands. m.c.vandergoes@umcutrecht.nl
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Consensus Development Conference
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