What is the dosage and treatment duration of Cefixime for various bacterial infections?

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Cefixime Dosing and Treatment Duration

Standard Adult Dosing

The FDA-approved dose of cefixime for adults is 400 mg daily, which can be administered as a single daily dose or divided into 200 mg twice daily. 1

  • The 400 mg capsule may be taken without regard to food 1
  • For infections caused by Streptococcus pyogenes, treatment must continue for at least 10 days to prevent rheumatic fever and glomerulonephritis 1

Pediatric Dosing (≥6 months old)

Children should receive 8 mg/kg/day of the oral suspension, administered either as a single daily dose or divided into 4 mg/kg every 12 hours. 1

  • Children weighing >45 kg or older than 12 years should receive the standard adult dose of 400 mg daily 1
  • For otitis media specifically, the suspension formulation must be used rather than tablets or capsules, as the suspension achieves higher peak blood levels at equivalent doses 1
  • Efficacy and safety have not been established in infants <6 months of age 1

Renal Impairment Dosing

Dose adjustment is required when creatinine clearance falls below 60 mL/min: 1

  • CrCl ≥60 mL/min: Normal dose (400 mg daily)
  • CrCl 21-59 mL/min OR hemodialysis: 260 mg daily (13 mL of 100 mg/5 mL suspension or 6.5 mL of 200 mg/5 mL suspension)
  • CrCl ≤20 mL/min OR peritoneal dialysis: 172 mg daily (8.6 mL of 100 mg/5 mL suspension or 4.4 mL of 200 mg/5 mL suspension)
  • Neither hemodialysis nor peritoneal dialysis removes significant amounts of cefixime 1

Specific Infection Indications and Durations

Uncomplicated Gonorrhea (Cervical/Urethral)

Cefixime should NOT be used as first-line therapy for gonorrhea due to declining susceptibility and suboptimal cure rates. 2, 3

  • If ceftriaxone is unavailable, use cefixime 400 mg orally as a single dose PLUS azithromycin 1 g orally 3
  • Cefixime achieves only 97.1-97.4% cure rates for urogenital/anorectal gonorrhea compared to 99.1% for ceftriaxone 2
  • Pharyngeal gonorrhea cure rate is only 91% with cefixime—avoid use for pharyngeal infections 2, 3
  • Mandatory test-of-cure at 1 week is required when cefixime is used 3
  • The CDC recommends against cefixime monotherapy due to rising minimum inhibitory concentrations (MICs), particularly in the Western United States and among men who have sex with men 2, 3

Uncomplicated Urinary Tract Infections

Cefixime 400 mg daily can be used for uncomplicated UTIs, though it provides lower blood and urinary concentrations than IV cephalosporins. 4, 1

  • Treatment duration typically 7-10 days for uncomplicated cystitis 5, 6
  • Urine culture and susceptibility testing should guide therapy 4
  • Should not be used empirically in areas with high resistance rates 4

Pharyngitis and Tonsillitis

For streptococcal pharyngitis, cefixime 400 mg daily (adults) or 8 mg/kg/day (children) must be continued for at least 10 days. 1

  • Clinical cure rates of 98.2% have been demonstrated in pediatric streptococcal pharyngitis 6
  • The 10-day duration is critical to prevent rheumatic fever complications 1

Acute Exacerbations of Chronic Bronchitis

Cefixime 400 mg daily for 7-14 days is effective for acute bacterial exacerbations of chronic bronchitis. 1, 7

  • Clinical success rates of 86-88% have been demonstrated 7
  • Effective against Haemophilus influenzae, Moraxella catarrhalis, and Streptococcus pneumoniae 7, 8

Otitis Media (Pediatric)

Children with acute otitis media should receive 8 mg/kg/day of cefixime suspension for 10 days. 1, 5

  • The suspension formulation is mandatory—do not substitute tablets or capsules 1
  • Comparable efficacy to cefaclor 20-40 mg/kg/day and amoxicillin 40 mg/kg/day 5

Enteric Fever (Typhoid)

The WHO recommends cefixime 8 mg/kg/day as a single daily dose for children >28 days, or 400 mg once daily for adults, for 7-14 days. 2

  • However, cefixime showed significantly more treatment failures and longer fever duration compared to fluoroquinolones in randomized trials 2
  • Consider alternative agents when available 2

Important Clinical Caveats

Pharmacokinetic Limitations

Cefixime provides lower and less sustained bactericidal levels than injectable ceftriaxone despite similar antimicrobial spectrum. 2, 4, 3

  • The 3-4 hour half-life permits once or twice daily dosing 5, 8
  • Peak concentration (Cmax) of 4.4 mcg/mL exceeds MIC90 for susceptible pathogens 8

Adverse Effects

Diarrhea and loose stools are the most common adverse effects, occurring in 16-24% of patients. 1, 9, 6

  • These effects are usually mild to moderate, transient, and occur in the first few days of treatment 5, 9
  • Drug discontinuation due to adverse effects occurs in only 1.9-2% of patients 9, 6
  • Clostridioides difficile-associated diarrhea can occur and requires evaluation if diarrhea develops 1

Spectrum Limitations

Cefixime has poor activity against Staphylococcus aureus, enterococci, Listeria monocytogenes, and Pseudomonas species. 5, 9

  • Excellent activity against beta-lactamase-producing strains of H. influenzae, N. gonorrhoeae, and Enterobacteriaceae 5, 8
  • Inactive against Pseudomonas aeruginosa 5, 9

Hypersensitivity Considerations

Cross-reactivity with penicillins occurs in up to 10% of penicillin-allergic patients—use with caution. 1

  • Anaphylactic reactions including shock and fatalities have been reported 1
  • Discontinue immediately if allergic reaction occurs 1

References

Guideline

Cefixime Treatment Recommendations

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Cefixime Indications and Limitations

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Oral Cephalosporin Regimens for Uncomplicated Urinary Tract Infections

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Cefixime.

DICP : the annals of pharmacotherapy, 1990

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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