| Indication |
Used to treat acute bacterial exacerbations of chronic bronchitis
(ABECB), acute bacterial otitis media, pharyngitis, and tonsilitis. |
| Pharmacodynamics |
Ceftibuten is a third-generation cephalosporin antibiotic. |
| Mechanism of action |
Ceftibuten exerts its bactericidal action by binding to essential
target proteins of the bacterial cell wall. This binding leads to
inhibition of cell-wall synthesis. |
| Absorption |
Rapidly absorbed following oral administration. |
| Volume of distribution |
- 0.21 L/kg [adult subjects]
- 0.5 L/kg [fasting pediatric patients]
|
| Protein binding |
Ceftibuten is 65% bound to plasma proteins. The protein binding is independent of plasma ceftibuten concentration. |
| Metabolism |
A study with radiolabeled ceftibuten administered to 6 healthy
adult male volunteers demonstrated that cis-ceftibuten is the
predominant component in both plasma and urine. About 10% of ceftibuten
is converted to the trans-isomer is approximately 1/8 as antimicrobially
potent as the cis-isomer. |
| Route of elimination |
Ceftibuten is excreted in the urine; 95% of the administered radioactivity was recovered either in urine or feces. |
| Half life |
Not Available |
| Clearance |
Not Available |
| Toxicity |
Overdosage of cephalosporins can cause cerebral irritation leading to convulsions |
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