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
  • 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

Common

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]

Group Organism Sensitivity
Gram Positive Strep. Group A, B, C, G S
Strep. Pneumoniae S
Viridans strep S
Strep. anginosus gp X1
Enterococcus faecalis R
Enterococcus faecium R
MSSA R
MRSA R
CA-MRSA R
Staph. Epidermidis R
C. jeikeium R
L. monocytogenes R
Gram Negatives N. gonorrhoeae S
N. meningitidis S
Moraxella catarrhalis S
H. influenzae S
E. coli S
Klebsiella sp S
E. coli/Klebsiella ESBL+ R
E coli/Klebsiella KPC+ R
Enterobacter sp, AmpC neg I
Enterobacter sp, AmpC pos R
Serratia sp I
Serratia marcescens I
Salmonella sp S
Shigella sp S
Proteus mirabilis S
Proteus vulgaris S
Providencia sp. S
Morganella sp. I
Citrobacter freundii R
Citrobacter diversus I
Citrobacter sp. R
Aeromonas sp S
Acinetobacter sp. R
Pseudomonas aeruginosa R
Burkholderia cepacia R
Stenotrophomonas maltophilia R
Yersinia enterocolitica S
Francisella tularensis X1
Brucella sp. X1
Legionella sp. R
Pasteurella multocida S
Haemophilus ducreyi X1
Vibrio vulnificus X1
Misc Chlamydophila sp R
Mycoplasm pneumoniae R
Rickettsia sp R
Mycobacterium avium R
Anaerobes Actinomyces X1
Bacteroides fragilis R
Prevotella melaninogenica I
Clostridium difficile X1
Clostridium (not difficile) I
Fusobacterium necrophorum X1
Peptostreptococcus sp. S

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

  1. Sanford Guide to Antimicrobial Therapy

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