What dose of Bactrim (trimethoprim‑sulfamethoxazole) pediatric suspension should be given to a 6‑year‑old child weighing 21.3 kg, and how often?

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Bactrim Liquid Dosing for a 21.3 kg, 6-Year-Old Child

For a 6-year-old child weighing 21.3 kg, administer Bactrim (trimethoprim-sulfamethoxazole) suspension at 8–12 mg/kg/day of the trimethoprim component (170–255 mg trimethoprim total daily), divided into 2 doses given every 12 hours. 1, 2

Practical Dosing Calculation

For standard infections (UTI, skin/soft tissue, otitis media):

  • Total daily trimethoprim dose: 21.3 kg × 8 mg/kg = 170 mg trimethoprim per day (lower end) to 21.3 kg × 12 mg/kg = 255 mg trimethoprim per day (higher end) 1, 2
  • Divided dose: Give 85–127.5 mg trimethoprim every 12 hours 1, 2

Using Bactrim pediatric suspension (40 mg trimethoprim/5 mL):

  • Lower dose: 85 mg ÷ 40 mg per 5 mL = 10.6 mL every 12 hours 2
  • Higher dose: 127.5 mg ÷ 40 mg per 5 mL = 16 mL every 12 hours 2

Practical recommendation: Start with 10–12 mL every 12 hours for mild-to-moderate infections, or 15–16 mL every 12 hours for more serious infections. 1, 2

Indication-Specific Adjustments

For mild-to-moderate infections (UTI, uncomplicated skin infections):

  • Use the lower dosing range (8–10 mg/kg/day trimethoprim) divided every 12 hours for 7–10 days 3, 1
  • This translates to approximately 10–12 mL of suspension every 12 hours 2

For serious infections (severe MRSA, complicated infections):

  • Use the higher dosing range (10–12 mg/kg/day trimethoprim) divided every 12 hours 3, 1
  • This translates to approximately 14–16 mL of suspension every 12 hours 2

For life-threatening infections (severe pneumonia, CNS infections):

  • Consider 15–20 mg/kg/day trimethoprim divided every 6–8 hours (not every 12 hours) 3, 1
  • This would require 4 divided doses per day rather than the standard twice-daily regimen 3

Treatment Duration

  • Standard infections: 7–14 days 3
  • UTI: 10–14 days 2
  • Shigellosis: 5 days 2
  • Otitis media: 10 days 2
  • Severe MRSA osteomyelitis: >6 weeks (typically combined with rifampin) 1

Critical Monitoring Requirements

Obtain baseline and monthly laboratory monitoring during prolonged therapy:

  • Complete blood count with differential and platelet count to assess for neutropenia, thrombocytopenia, and anemia 3, 1, 4
  • Most adverse reactions develop within the first 2 weeks of therapy 5

Ensure adequate hydration:

  • Patient should drink at least 1.5 liters of fluid daily to prevent crystalluria, especially with higher doses 1

Important Safety Considerations and Contraindications

Absolute contraindications:

  • Age <2 months (risk of kernicterus from sulfonamide displacement of bilirubin) 6, 2
  • Known hypersensitivity to sulfonamides or trimethoprim 6

Use with extreme caution in:

  • G6PD deficiency: Screen before initiating therapy due to hemolytic anemia risk 1, 6, 4
  • Renal insufficiency: Requires dose adjustment (see below) 1, 2
  • Hepatic insufficiency: Avoid in severe hepatic impairment 1, 6

Renal Impairment Dose Adjustments

If creatinine clearance is reduced:

  • CrCl 15–30 mL/min: Reduce dose by 50% 1, 2
  • CrCl <15 mL/min: Reduce dose by 50% or use alternative agent 1, 2
  • CrCl <10 mL/min: Use is not recommended per FDA label, though reduced dosing may be considered clinically 2

Management of Adverse Reactions

For mild rash:

  • Temporarily discontinue and restart when resolved 3, 4
  • Some patients can be successfully desensitized if rechallenge is necessary 3

For life-threatening reactions (anaphylaxis, Stevens-Johnson syndrome, urticarial rash, hypotension):

  • Permanently discontinue the drug 3, 4

Common adverse effects (occur in ~15% of patients):

  • Dermatologic reactions (rash) 6, 4
  • Hematologic effects (neutropenia, thrombocytopenia) 6, 4, 5
  • Gastrointestinal complaints (nausea, vomiting) 6, 5
  • Hepatic effects (hepatitis) 4
  • Renal effects (interstitial nephritis) 4

Key Drug Interactions

Exercise caution when co-administering with:

  • Methotrexate: Increased methotrexate toxicity 1, 6
  • Warfarin and other anticoagulants: Enhanced anticoagulant effect 1, 6
  • Oral hypoglycemics: Increased hypoglycemia risk 1, 6
  • Thiazide diuretics: Increased risk of thrombocytopenia 6
  • Anticonvulsants (phenytoin): Altered phenytoin levels 6

Formulation Considerations

The liquid formulation is strongly preferred for this patient:

  • Pediatric suspension allows accurate weight-based dosing for children <16 kg and provides flexibility for dose titration 1
  • Standard Bactrim pediatric suspension contains 40 mg trimethoprim + 200 mg sulfamethoxazole per 5 mL 2
  • Tablets are less practical for precise dosing in young children 1

Clinical Pearls

Pharmacokinetic data support the standard 8–12 mg/kg/day regimen:

  • This dosing achieves therapeutic targets for bacteria with MIC ≤0.5 mg/L in >90% of children 7
  • The exposure matches adult dosing of 320 mg trimethoprim twice daily 7

For bacteria with higher MIC (up to 1 mg/L):

  • Consider 12–15 mg/kg/day trimethoprim divided every 12 hours in children 6 years and older 7

References

Guideline

Bactrim Dosage and Administration

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Sulfatrim Pediatric Dosing Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Drug therapy reviews: trimethoprim-sulfamethoxazole.

American journal of hospital pharmacy, 1979

Guideline

Pediatric Dosage of Sulfaprim (Trimethoprim/Sulfamethoxazole)

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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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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