Trovafloxacin is a fluoroquinolone antibacterial agent with a broad sp
ectrum of activity. Trovafloxacin has similar or 2-fold lower activity
than ciprofloxacin against Enterobacteriaceae and Pseudomonas aerugin
osa. Against Haemophilus influenzae and Moraxella catarrhalis, trovafl
oxacin has similar activity to ciprofloxacin. Other susceptible Gram-n
egative pathogens include Neisseria gonorrhoeae, Chlamydia trachomatis
and mycoplasmas. The drug is active against Gram-positive bacteria an
d consistently displayed greater activity (2- to 8-fold) than ciproflo
xacin against all staphylococci and streptococci tested; activity incl
uded methicillin-resistant staphylococci and penicillin-resistant Stre
ptococcus pneumoniae. Trovafloxacin has some activity against vancomyc
in-resistant enterococci. Anaerobes such as Bacteroides and Clostridiu
m spp. are also susceptible to trovafloxacin. Preliminary clinical dat
a suggest that trovafloxacin is effective in the treatment of patients
with upper and lower respiratory tract and uncomplicated urinary trac
t infections and infections caused by C. trachomatis or N. gonorrhoeae
. The most frequently noted adverse event with trovafloxacin is dizzin
ess which is reported in 11% of patients versus 3% of those receiving
comparator agents. Other commonly reported events (>1% of patients) ar
e nausea, headache, vomiting, vaginitis and diarrhoea.