Cefradine

General

  • Type: 1st generation Cephalosporin
  • Dosage Forms: Capsules, Oral Suspension, Powder for injection
  • Dosage Strengths: 250mg, 500mg; 125mg/5ml, 250mg/5ml; 500mg, 1g vials
  • Routes of Administration: PO, IV, IM
  • Common Trade Names: Velosef, Nicef

Adult Dosing

General

  • Mild: 250-500mg PO q6h or 500mg-1g PO q12h
  • Mod-Severe: 500mg-1g IM/IV q6h
  • Max: 8g/day (IV), 4g/day (PO)

UTI, Uncomplicated

  • 500mg PO q12h

Respiratory Tract Infections

  • 250mg PO q6h or 500mg PO q12h

Skin and Soft Tissue

  • 250mg PO q6h or 500mg PO q12h

Surgical Prophylaxis

  • 1-2g IM/IV x1 (30-90 min before procedure)
  • May repeat q4-6h for up to 24h

Pediatric Dosing

General (>9 Months)

  • 25-50mg/kg/day PO/IM/IV divided q6h or q12h
  • Severe: 75-100mg/kg/day PO/IM/IV divided q6h
  • Max: 4g/day

Special Populations

  • Pregnancy: B
  • Lactation: Excreted in breast milk; use with caution
  • Renal
    • Adult
      • CrCl >20: dose unchanged
      • CrCl 5-20: 250-500mg q6h (PO) or 50% of dose (IV)
      • CrCl <5: 250-500mg q12h (PO) or 25% of dose (IV)
      • Hemodialysis: Give dose after dialysis (250mg start, then 250mg q12h)
      • Peritoneal dialysis: Resistant to dialysis
    • Pediatric
      • Renal dosing adjustment required; specific guidelines vary, generally increase interval
  • Hepatic
    • Not defined

Contraindications

  • Allergy to class/drug (Cephalosporins)
  • Immediate hypersensitivity to Penicillins

Adverse Reactions

Serious

Common

Pharmacology

  • Half-life: 0.7 - 1.3h (Extended in renal failure)
  • Metabolism: Not significantly metabolized
  • Excretion: Urine (>90% unchanged)
  • Mechanism of Action: Bactericidal; inhibits cell wall mucopeptide synthesis

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 S
MRSA R
CA-MRSA R
Staph. Epidermidis I
C. jeikeium R
L. monocytogenes R
Gram Negatives N. gonorrhoeae I
N. meningitidis R
Moraxella catarrhalis I
H. influenzae I
E. coli S
Klebsiella sp S
E. coli/Klebsiella ESBL+ R
E coli/Klebsiella KPC+ R
Enterobacter sp, AmpC neg R
Enterobacter sp, AmpC pos R
Serratia sp R
Serratia marcescens R
Salmonella sp X1
Shigella sp X1
Proteus mirabilis S
Proteus vulgaris R
Providencia sp. R
Morganella sp. R
Citrobacter freundii R
Citrobacter diversus R
Citrobacter sp. R
Aeromonas sp R
Acinetobacter sp. R
Pseudomonas aeruginosa R
Burkholderia cepacia R
Stenotrophomonas maltophilia R
Yersinia enterocolitica R
Francisella tularensis X1
Brucella sp. X1
Legionella sp. R
Pasteurella multocida X1
Haemophilus ducreyi R
Vibrio vulnificus X1
Misc Chlamydophila sp R
Mycoplasm pneumoniae R
Rickettsia sp R
Mycobacterium avium R
Anaerobes Actinomyces X1
Bacteroides fragilis R
Prevotella melaninogenica X1
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