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. Author manuscript; available in PMC: 2015 Nov 6.
Published in final edited form as: Pharmacoepidemiol Drug Saf. 2013 Aug 20;22(10):1099–1106. doi: 10.1002/pds.3499

Table 3.

Count of NEISS-CADES Cases and Projected National Estimates of US Emergency Department Visits Stratified by Fluoroquinolone and Hypersensitivity Reaction Severity Category, 2004–2010

All Reaction Severity Categories Mild Reactions Moderate to Severec Reactions
Fluoroquinolone Number of NEISS-CADES Cases Estimated Number of ED Visits (95% CI) Number of NEISS-CADES Cases Estimated Number of ED Visits (95% CI) Number of NEISS-CADES Cases Estimated Number of ED Visits (95% CI)
Ciprofloxacin 469 32,269 (25,271–39,265) 321 22,523 (16,906–28,138) 148 9,746 (7,247–12,244)
Levofloxacin 505 35,947 (27,617–44,276) 311 22,028 (16,499–27,556) 194 13,918 (10,164–17,672)
Moxifloxacin 448 34,469 (24,148–44,789) 265 20,104 (12,966–27,212) 183 14,365 (9,781–18,948)
All Analyzablea Fluoroquinolones 1422 102,684 (81,026–124,342) 897 64,655 (50,819–78,490) 525 38,029 (28,539–47,518)
All Fluoroquinolonesb 1440 104,338 (82,047–126,628) 910 65,901 (51,750–80,051) 530 38,437 (28,680–48,194)

Source data: NEISS-CADES database 2004–2010 Extracted November 9, 2012

a

Includes cases attributed to ciprofloxacin, levofloxacin and moxifloxacin only.

b

Includes cases attributed to ciprofloxacin, levofloxacin, moxifloxacin, gemifloxacin and ofloxacin. There were no cases of norfloxacin attributed hypersensitivity in the NEISS-CADES system.

c

Moderate to severe reactions are pooled cases of moderate and severe reactions from the NEISS-CADES system.