Cefixime is an orally active third generation cephalosporin with in vi
tro antibacterial activity against most important lower respiratory pa
thogens. The drug is active against Haemophilus influenzae, Moraxella
catarrhalis and penicillin-susceptible Streptococcus pneumoniae but no
t Staphylococcus aureus. Cefixime has a long elimination half-life (3
hours compared with 0.5 hours for cefaclor and 1.5 hours for cefalexin
), which allows once daily administration. Several trials have establi
shed the clinical efficacy of the drug in patients with lower respirat
ory tract infection (LRTI). In comparative studies cefixime had simila
r efficacy to amoxicillin +/- clavulanic acid, cefaclor; cefalexin, ce
furoxime axetil and clarithromycin. Trials evaluating the efficacy of
cefixime as the oral component of intravenous to oral switch therapy h
ave produced promising preliminary results although further carefully
designed trials are needed in this area. As with certain other drugs o
f its class, gastrointestinal disturbances are the most frequently rep
orted adverse events in patients taking cefixime and cases of pseudome
mbranous colitis have been reported. Thus, cefixime is an effective tr
eatment for mild to moderate LRTI and may have a role as the oral comp
onent of intravenous to oral switch therapy although further well desi
gned studies are needed to confirm initial favourable results in this
important emerging area of antibacterial therapy.