What is the dosage and treatment duration of Taxim O (cefotaxime) for typhoid fever?

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Treatment of Typhoid Fever with Taxim-O (Cefixime)

For uncomplicated typhoid fever, Taxim-O (cefixime) should be dosed at 8 mg/kg/day (maximum 400 mg/day) as a single daily dose for 7-14 days, though it is less effective than azithromycin or ceftriaxone and should be reserved as an alternative option when first-line agents cannot be used. 1

Dosing Regimen

  • Standard dose: 8 mg/kg/day as a single daily dose for 7-14 days 1
  • Alternative regimen from clinical trials: 20 mg/kg/day divided into two doses (every 12 hours) for a minimum of 12 days showed clinical cure in 50 children, with fever subsiding within a mean of 5.3 days 2
  • The longer duration (12-14 days) may be preferable to reduce relapse risk, as only 2 of 50 patients relapsed with the 12-day regimen 2

Position in Treatment Algorithm

Cefixime is not a first-line agent for typhoid fever, particularly in regions with high fluoroquinolone resistance like India and South Asia:

  • First-line therapy: Azithromycin 20 mg/kg/day (maximum 1g/day) orally for 7 days is preferred, with a 94% cure rate and lower relapse risk (OR 0.09) compared to ceftriaxone 1
  • For severe cases: Ceftriaxone 50-80 mg/kg/day (maximum 2g/day) IV for 5-7 days, transitioning to oral therapy once afebrile for 24 hours 1
  • Cefixime as alternative: Use when azithromycin is unavailable or contraindicated for uncomplicated cases 1

Clinical Efficacy Considerations

The evidence for cefixime shows it is less effective than fluoroquinolones but still clinically useful:

  • In a Vietnamese trial comparing cefixime (7 days) versus ofloxacin (5 days), treatment failures were significantly higher with cefixime, and days of fever, poor eating, and immobility were significantly longer 3
  • However, cefixime demonstrated 96% clinical cure (48/50 patients) in children with multidrug-resistant S. typhi, including chloramphenicol-resistant strains 2
  • Expected fever clearance: 4-5 days with appropriate therapy; cefixime averaged 5.3 days in clinical trials 1, 2

Critical Pitfalls to Avoid

  • Do not use fluoroquinolones empirically in patients returning from India or South Asia, where resistance exceeds 70% 4, 1
  • Obtain blood cultures before starting antibiotics when possible, as they have the highest yield (40-80% sensitivity) within the first week of symptoms 1
  • Monitor for complications (gastrointestinal bleeding, intestinal perforation, encephalopathy) which occur in 10-15% of patients, especially if illness duration exceeds 2 weeks 4, 1
  • Relapse risk: Occurs in approximately 4% of cefixime-treated patients; monitor for 8 weeks post-treatment 2

When to Escalate Therapy

If the patient remains febrile beyond 4-5 days or shows clinical deterioration:

  • Switch to IV ceftriaxone 2g daily (adults) or 50-80 mg/kg/day (children) for 14 days to reduce relapse risk 4
  • Consider combination therapy with ciprofloxacin and cefotaxime for severe cases, which shows synergistic effects in vitro against nalidixic acid-resistant strains 5

References

Guideline

Treatment Guidelines for Typhoid Fever in India

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Cefixime in the treatment of enteric fever in children.

Drugs under experimental and clinical research, 1993

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Typhoid Fever Treatment Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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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