Gatifloxacin is a novel extended-spectrum fluoroquinolone with improved Gra
m-positive and anaerobe coverage compared with older agents such as ciprofl
oxacin. It has good activity (but is slightly less active than ciprofloxaci
n) against Enterobacteriaceae.
Gatifloxacin is generally 2- to 4-fold more active than ciprofloxacin again
st staphylococci, streptococci and enterococci and 4- to 16-fold more activ
e than ciprofloxacin against anaerobes, including Clostridium and Bacteroid
es spp.
In comparative clinical trials that included patients with lower respirator
y tract, urinary tract, skin and soft tissue or gonococcal infections, clin
ical cure rates of greater than or equal to 89% were achieved with oral gat
ifloxacin 400 mg/day for 7 to 14 days.
Data from a subset of North American patients included in a multinational t
rial showed that oral gatifloxacin 400 mg/day produced a significantly high
er clinical cure rate than cefuroxime axetil 250mg twice daily (89 vs 77%;
p = 0.01) in patients with acute exacerbations of chronic bronchitis. The c
linical efficacy of gatifloxacin was similar to that of clarithromycin or l
evofloxacin or ceftriaxone (with or without erythromycin) in the treatment
of patients with community-acquired pneumonia.
Oral gatifloxacin 400 mg/day showed clinical and bacteriological efficacy s
imilar to that of levofloxacin in patients with skin and soft tissue infect
ions. In patients with urinary tract infections, clinical cure and bacteria
l eradication rates achieved with a single 400mg oral dose of gatifloxacin
were similar to those produced with ciprofloxacin.
In a pooled analysis of tolerability data from trials that included 3021 pa
tients treated with oral gatifloxacin 400 mg/day, the most commonly reporte
d adverse events were nausea (8%), diarrhoea (4%), headache (4%) and dizzin
ess (3%). The drug was reported to be well tolerated. Gatifloxacin does not
appear to cause phototoxic effects.