pubmed-article:21373193 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:21373193 | lifeskim:mentions | umls-concept:C0031809 | lld:lifeskim |
pubmed-article:21373193 | lifeskim:mentions | umls-concept:C1882071 | lld:lifeskim |
pubmed-article:21373193 | lifeskim:mentions | umls-concept:C0003385 | lld:lifeskim |
pubmed-article:21373193 | lifeskim:mentions | umls-concept:C0878773 | lld:lifeskim |
pubmed-article:21373193 | lifeskim:mentions | umls-concept:C0877248 | lld:lifeskim |
pubmed-article:21373193 | lifeskim:mentions | umls-concept:C1522326 | lld:lifeskim |
pubmed-article:21373193 | lifeskim:mentions | umls-concept:C0449445 | lld:lifeskim |
pubmed-article:21373193 | pubmed:issue | 2 | lld:pubmed |
pubmed-article:21373193 | pubmed:dateCreated | 2011-3-4 | lld:pubmed |
pubmed-article:21373193 | pubmed:abstractText | Overactive bladder (OAB) affects the lives of millions of people worldwide and antimuscarinics are the pharmacological treatment of choice. Meta-analyses of all currently used antimuscarinics for treating OAB found similar efficacy, making the choice dependent on their adverse event profiles. However, conventional meta-analyses often fail to quantify and compare adverse events across different drugs, dosages, formulations, and routes of administration. In addition, the assessment of the broad variety of adverse events is dissatisfying. Our aim was to compare adverse events of antimuscarinics using a network meta-analytic approach that overcomes shortcomings of conventional analyses. | lld:pubmed |
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pubmed-article:21373193 | pubmed:language | eng | lld:pubmed |