Amoxicillin-Clavulanate Dosing for Bacterial Infections
For most adult bacterial infections, prescribe amoxicillin-clavulanate 875/125 mg twice daily, taken at the start of meals to minimize gastrointestinal side effects. 1, 2, 3
Standard Adult Dosing Regimens
First-Line Dosing
- 875/125 mg twice daily is the standard dose for most bacterial infections in adults, including respiratory tract infections, sinusitis, skin and soft tissue infections, and bite wounds 1, 2, 3
- An alternative regimen of 500/125 mg three times daily may be used, particularly for respiratory tract infections 2
- Take at the start of meals to enhance clavulanate absorption and reduce gastrointestinal intolerance 3
High-Dose Therapy for Resistant Pathogens
Use 2000/125 mg twice daily when antibiotic resistance is likely, including: 4
- Recent antibiotic use within the past 30 days
- Recent healthcare contact or hospitalization
- High community prevalence of resistant Streptococcus pneumoniae (>10%)
- Age >65 years or immunocompromised status
- Moderate to severe infections (frontal/sphenoidal sinusitis)
- Comorbidities (diabetes, chronic heart/lung/liver/kidney disease)
This high-dose formulation achieves adequate serum concentrations to eradicate penicillin-resistant S. pneumoniae with MICs up to 4-8 mg/L 4
Pediatric Dosing
Standard Pediatric Dosing (≥12 weeks)
- Less severe infections: 25 mg/kg/day every 12 hours or 20 mg/kg/day every 8 hours 4
- More severe infections: 45 mg/kg/day every 12 hours or 40 mg/kg/day every 8 hours 4, 2
- Calculate dose based on actual body weight, not age, to avoid underdosing 2
High-Dose Pediatric Therapy
Use 90 mg/kg/day of amoxicillin with 6.4 mg/kg/day of clavulanate in two divided doses for: 4
- Acute bacterial rhinosinusitis
- Acute otitis media with recent antibiotic use (within 30 days)
- Otitis-conjunctivitis syndrome
- Age <2 years with risk factors
- Daycare attendance
- Areas with high penicillin-resistant S. pneumoniae prevalence
Infection-Specific Dosing and Duration
Respiratory Tract Infections
- Acute bacterial rhinosinusitis (adults): 875/125 mg twice daily for 5-7 days 1, 4, 2
- Acute bacterial rhinosinusitis (children): 90 mg/kg/day for 10-14 days 4
- Community-acquired pneumonia (moderate severity): 875/125 mg twice daily or 500/125 mg three times daily for 7-10 days 4, 2
- COPD exacerbations: Co-amoxiclav as first-line treatment for moderate-severe exacerbations without Pseudomonas risk 4
Skin and Soft Tissue Infections
- Animal or human bites: 875/125 mg twice daily for 5-7 days 1
- General skin/soft tissue infections: Treat for 5-7 days after clinical improvement 1
Intra-Abdominal Infections
Urinary Tract Infections
- Uncomplicated UTI: 3-7 days of therapy 4
Intravenous Dosing
Hospital-Based IV Therapy
- Moderate to severe infections: 1.2 g IV every 8 hours (three times daily) 1
- Critically ill patients or severe sepsis: Consider every 6 hours (QID) dosing for optimal bacterial killing 1
- Mild to moderate uncomplicated infections: BID dosing may be acceptable in outpatient settings 1
Special Populations
Renal Impairment
- Patients with GFR <30 mL/min should not receive the 875 mg dose 3
- Dose reduction generally not required unless renal impairment is severe 3
Administration Pearls
Optimizing Tolerability
- Administer at the start of meals to minimize gastrointestinal side effects 2, 3
- Twice-daily dosing (875/125 mg) is associated with less moderate-to-severe diarrhea compared to three-times-daily dosing (500/125 mg) 5
- Oral suspension must be shaken well before each use and refrigerated 2
- Reconstituted suspension expires after 14 days 2
Clinical Monitoring
- Evaluate clinical response within 48-72 hours of initiating therapy 4
- If no improvement, consider alternative management or high-dose therapy 4
Critical Pitfalls to Avoid
- Never underdose in children: Always calculate based on actual body weight, not age 2
- Avoid standard dosing in high-resistance areas: Use high-dose formulations when penicillin-resistant S. pneumoniae prevalence exceeds 10% 4
- Do not use 875 mg dose in severe renal impairment (GFR <30 mL/min) 3
- Avoid co-administration with probenecid, and monitor prothrombin time with oral anticoagulants 1