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. 1999 May-Jun;10(3):207–238. doi: 10.1155/1999/378394

TABLE 8.

Frequently occurring adverse effects of the new fluoroquinolones and ciprofloxacin

Adverse effect Fluoroquinolone
Ciprofloxacin Clinafloxacin Gatifloxacin Grepafloxacin Levofloxacin Moxifloxacin Sparfloxacin Trovafloxacin
Gastrointestinal
  Nausea + ND + + + + + + + + +
  Vomiting + ND ND + +/− +/− + +
  Diarrhea + + + + + + + + + +
Central nervous system
  Dizziness + ND + + +/− + + +
  Headache + ND + + + +/− + +
Allergic
  Rash + ND ND + +/− + +/−
  Pruritis +/− ND ND + +/− +/− +/−
Phototoxicity +/− + + +/ND + +/− +/− + + +/−
Cardiovascular (QTc prolongation)* ND ND + + + ND
Taste perversion ND ND + + + +/− ND
Injection site reaction + + NA NA + NA NA +/−
*

Percentages of patients experiencing this side effect have not been documented for both sparfloxacin and grepafloxacin. The relative number of “+” symbols here only indicates that there are more reports of this side effect with sparfloxacin.

Side effect has not been observed;

+/−

Side effect occurs in less than 1% of patients;

+

Side effect occurs in 1% to 5% of patients;

+ +

Side effect occurs in 6% to 10% of patients;

+ + +

Side effect occurs in more than 10% of patients;

+/ND

Side effect is expected to occur but has not been documented yet. For clinafloxacin, gatifloxacin, moxifloxacin and trovafloxacin, because these agents have not been extensively studied in clinical trials, if a specific side effect was not found to be reported a ‘ND’ was entered into the table. For ciprofloxacin, grepafloxacin, levofloxacin and sparfloxacin, a ‘−’ was entered into the Table if a specific side effect was not found to be reported because these agents have been extensively studied in clinical trials.

NA Not applicable (fluoroquinolone is not available in an intravenous formulation);

ND No data.

Adapted from references 6,144,145,162164,166,169,171,190,213,216224