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Maxipime: Product Label Information (NDA no. 0506679). Available viahttp:\/\/www.accessdata.fda.gov\/scripts\/cder\/drugsatfda\/index.cfm. Updated May 1 2014."},{"key":"e_1_2_6_8_1","doi-asserted-by":"publisher","DOI":"10.3904\/kjim.2012.27.3.367"},{"key":"e_1_2_6_9_1","doi-asserted-by":"publisher","DOI":"10.1093\/ndt\/gfm713"},{"key":"e_1_2_6_10_1","doi-asserted-by":"publisher","DOI":"10.1128\/AAC.01595-08"},{"key":"e_1_2_6_11_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.mcn.2014.10.001"},{"key":"e_1_2_6_12_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0028-3908(03)00188-6"},{"key":"e_1_2_6_13_1","doi-asserted-by":"publisher","DOI":"10.1038\/clpt.1990.149"},{"key":"e_1_2_6_14_1","doi-asserted-by":"publisher","DOI":"10.1186\/1471-2334-14-288"},{"key":"e_1_2_6_15_1","unstructured":"U.S. Department of Health & Human Services.FDA Drug Safety Communication: Cefepime and risk of seizure in patients not receiving dosage adjustments for kidney impairment. 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