pubmed-article:8556111 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:8556111 | lifeskim:mentions | umls-concept:C0700287 | lld:lifeskim |
pubmed-article:8556111 | lifeskim:mentions | umls-concept:C0041755 | lld:lifeskim |
pubmed-article:8556111 | lifeskim:mentions | umls-concept:C0033213 | lld:lifeskim |
pubmed-article:8556111 | lifeskim:mentions | umls-concept:C2936612 | lld:lifeskim |
pubmed-article:8556111 | lifeskim:mentions | umls-concept:C1551358 | lld:lifeskim |
pubmed-article:8556111 | pubmed:issue | 10 | lld:pubmed |
pubmed-article:8556111 | pubmed:dateCreated | 1996-2-26 | lld:pubmed |
pubmed-article:8556111 | pubmed:abstractText | The objectives of this study were 1) to determine the frequency with which adverse drug events result in an incident report (IR) in hospitalized patients; and 2) to determine if there were differences between quality assurance administrators, nurse leaders in quality assurance, and staff nurses as to whether an incident report should or would be filed for each adverse drug event. | lld:pubmed |
pubmed-article:8556111 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8556111 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8556111 | pubmed:language | eng | lld:pubmed |
pubmed-article:8556111 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8556111 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:8556111 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:8556111 | pubmed:month | Oct | lld:pubmed |
pubmed-article:8556111 | pubmed:issn | 1070-3241 | lld:pubmed |
pubmed-article:8556111 | pubmed:author | pubmed-author:CullenD JDJ | lld:pubmed |
pubmed-article:8556111 | pubmed:author | pubmed-author:LeapeL LLL | lld:pubmed |
pubmed-article:8556111 | pubmed:author | pubmed-author:BatesD WDW | lld:pubmed |
pubmed-article:8556111 | pubmed:author | pubmed-author:CooperJ BJB | lld:pubmed |
pubmed-article:8556111 | pubmed:author | pubmed-author:NemeskalA RAR | lld:pubmed |
pubmed-article:8556111 | pubmed:author | pubmed-author:SmallS DSD | lld:pubmed |
pubmed-article:8556111 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:8556111 | pubmed:volume | 21 | lld:pubmed |
pubmed-article:8556111 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:8556111 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:8556111 | pubmed:pagination | 541-8 | lld:pubmed |
pubmed-article:8556111 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
pubmed-article:8556111 | pubmed:meshHeading | pubmed-meshheading:8556111-... | lld:pubmed |
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pubmed-article:8556111 | pubmed:meshHeading | pubmed-meshheading:8556111-... | lld:pubmed |
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pubmed-article:8556111 | pubmed:meshHeading | pubmed-meshheading:8556111-... | lld:pubmed |
pubmed-article:8556111 | pubmed:meshHeading | pubmed-meshheading:8556111-... | lld:pubmed |
pubmed-article:8556111 | pubmed:year | 1995 | lld:pubmed |
pubmed-article:8556111 | pubmed:articleTitle | The incident reporting system does not detect adverse drug events: a problem for quality improvement. | lld:pubmed |
pubmed-article:8556111 | pubmed:affiliation | Harvard Medical School, Massachusetts General Hospital, Boston, USA. | lld:pubmed |
pubmed-article:8556111 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:8556111 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
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