1999
DOI: 10.1345/aph.17460
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Trovafloxacin: A New Fluoroquinolone

Abstract: The advantages of once-daily dosing and enhanced activity of trovafloxacin against gram-positive and anaerobic organisms may expand its use over available fluoroquinolones. Further studies are needed to define its role in the treatment of various infectious diseases.

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Cited by 21 publications
(6 citation statements)
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“…ALA is the prodrug of TRO and is suitable for intravenous administration owing to its enhanced solubility in water; in this case, the conversion of ALA into TRO rapidly takes place in plasma after intravenous administration. Both prodrugs (PRU and ALA) are undetectable in systemic circulation after administration or, in the particular case of ALA, 5 min after the infusion [31,34,35]. Because fluoroquinolones are not highly protein-bound and their metabolism by the cytochrome P450 (CYP) system is limited to the CYP1A2 isoenzyme, fluoroquinolone interactions with other drugs are somewhat minimized [7].…”
Section: Pharmacokinetic and Pharmacodynamic Propertiesmentioning
confidence: 99%
“…ALA is the prodrug of TRO and is suitable for intravenous administration owing to its enhanced solubility in water; in this case, the conversion of ALA into TRO rapidly takes place in plasma after intravenous administration. Both prodrugs (PRU and ALA) are undetectable in systemic circulation after administration or, in the particular case of ALA, 5 min after the infusion [31,34,35]. Because fluoroquinolones are not highly protein-bound and their metabolism by the cytochrome P450 (CYP) system is limited to the CYP1A2 isoenzyme, fluoroquinolone interactions with other drugs are somewhat minimized [7].…”
Section: Pharmacokinetic and Pharmacodynamic Propertiesmentioning
confidence: 99%
“…This association is supported primarily by the time course of the leukopenia (5 d after initiation of therapy) and its resolution (60 h after administration of last dose), which is consistent with the reported half-life of trovafloxacin in healthy patients and patients with normal liver function (~10 h). 6 The attribution of leukopenia to trovafloxacin is also supported by the exclusion of other potential causes of an acute decrease in the number of circulating leukocytes. One such cause could have been medications other than trovafloxacin.…”
Section: Discussionmentioning
confidence: 99%
“…Indeed there is enough evidence to suggest that the study cannot be flawed on efficacy and tolerability issues. 43 In our view the scientific problem with the study was the apparent deficiency in concern for safety. Fluoroquinolones are not approved by the FDA for children, and trovafloxacin is not an exception.…”
Section: Scientific Validitymentioning
confidence: 99%