Cefaloglycin
General
- Type: 1st generation Cephalosporin
- Dosage Forms: capsule
- Dosage Strengths: 250mg, 500mg
- Routes of Administration: PO
- Common Trade Names: Kefoglycin
Adult Dosing
General
- Mild-Mod: 250mg PO q6h
- Severe: 500mg PO q6h
- Max: 4g/day
UTI, Uncomplicated
- 250-500mg PO q6h
Pediatric Dosing
General (>1 Month)
- 25-50mg/kg/day PO divided q6h
- Max: 4g/day
Special Populations
- Pregnancy: B
- Lactation: Excreted in breast milk; use caution
- Renal
- Adult
- CrCl <10 or significant impairment: Modify interval (data limited on specific adjustments, often avoided in severe failure due to ineffective urine concentrations)
- Adult
- Hepatic
- Not defined
Contraindications
- Allergy to class/drug
Adverse Reactions
Serious
- Anaphylaxis
- Stevens-Johnson Syndrome
- Clostridium difficile Associated Diarrhea
- Neutropenia
- Nephrotoxicity (rare)
Common
- Diarrhea (Higher incidence compared to other cephalosporins)
- Nausea and Vomiting
- Abdominal Pain
- Rash
- Urticaria
- Dyspepsia
- Glossitis
Pharmacology
- Half-life: 1.5h
- Metabolism: Limited hepatic metabolism; deacetylated to desacetylcephaloglycin
- Excretion: Urine (excreted unchanged)
- Mechanism of Action: Bactericidal; binds to penicillin binding proteins and inhibits cell wall mucopeptide synthesis
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
