| 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 |
|
| 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 |
Saturday, October 13, 2012
Pharmacology Of Ceftibuten
Labels:
Pharmacology of Drugs,
UNCLASSIFIED
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