Cefetamet
General
- Type: 3rd generation Cephalosporin
- Dosage Forms: Tablet, Powder for oral suspension
- Dosage Strengths: 250mg, 500mg (dosed as cefetamet pivoxil)
- Routes of Administration: PO
- Common Trade Names: Globor
Adult Dosing
General
- Standard: 500mg PO q12h
- Administer with food (increases bioavailability)
- Max: 2000mg/day
Community Acquired Pneumonia
- 500mg PO q12h x 10 days
Acute Bacterial Exacerbation of Chronic Bronchitis
- 500mg PO q12h x 7 days
Acute Sinusitis / Pharyngitis
- 500mg PO q12h x 7-10 days
UTI, Complicated and Uncomplicated
- 500mg PO q12h x 7-10 days
Uncomplicated Gonorrhea
- 1200-1500mg PO x 1 (Single dose)
Pediatric Dosing
General (>3 Months)
- 10mg/kg PO q12h
- Administer with food
- Max: 1000mg/day (Administer as tablet if child can swallow, or suspension)
Acute Otitis Media
- 10mg/kg PO q12h x 7-10 days
Pharyngitis / Tonsillitis
- 10mg/kg PO q12h x 7-10 days
Special Populations
- Pregnancy: B (Use only if clearly needed)
- Lactation: Excreted in breast milk; caution advised
- Renal
- Adult
- CrCl > 40: Standard dose (500mg q12h)
- CrCl 10-39: 125mg q12h OR 500mg q24h
- CrCl < 10: 125mg q24h OR 500mg q48h
- Hemodialysis: Give supplement after dialysis
- Pediatric
- CrCl > 40: Standard dose
- CrCl < 40: Extend interval or reduce dose similar to adult proportions
- Adult
- Hepatic
- No adjustment necessary (metabolism is ester hydrolysis in intestinal wall/serum, not hepatic CYP dependent)
Contraindications
- Allergy to class/drug (Cephalosporins)
- History of severe hypersensitivity to Penicillin
- Known Carnitine deficiency (due to pivoxil pivalate liberation)
Adverse Reactions
Serious
- Anaphylaxis
- Stevens-Johnson Syndrome
- Clostridium difficile associated diarrhea
- Hypocarnitinemia (Long term use)
- Angioedema
Common
- Diarrhea
- Nausea and Vomiting
- Abdominal Pain
- Dyspepsia
- Headache
- Fatigue
Pharmacology
- Half-life: 2-3h (Prolonged in renal impairment)
- Metabolism: Cefetamet pivoxil is a prodrug; hydrolyzed by esterases in the intestinal wall to active Cefetamet (and pivalic acid).
- Excretion: Urine (>85% as unchanged active drug)
- Mechanism of Action: Bactericidal; inhibits cell wall mucopeptide synthesis.
- Notes: Poor activity against Staphylococci compared to other cephalosporins.
Antibiotic Sensitivities[1]
Key
- S susceptible/sensitive (usually)
- I intermediate (variably susceptible/resistant)
- R resistant (or not effective clinically)
- S+ synergistic with cell wall antibiotics
- U sensitive for UTI only (non systemic infection)
- X1 no data
- X2 active in vitro, but not used clinically
- X3 active in vitro, but not clinically effective for Group A strep pharyngitis or infections due to E. faecalis
- X4 active in vitro, but not clinically effective for strep pneumonia
See Also
References
- ↑ Sanford Guide to Antimicrobial Therapy
```
