What dose of Augmentin (amoxicillin/clavulanate) suspension should an otherwise healthy adult with acute bacterial sinusitis receive?

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Augmentin Suspension Dosing for Adult Acute Bacterial Sinusitis

For an otherwise healthy adult with acute bacterial sinusitis, prescribe Augmentin 875 mg/125 mg orally twice daily for 5–7 days, or use the liquid suspension equivalent of 28 mL of the 125 mg/31.25 mg per 5 mL formulation twice daily if the patient cannot swallow tablets. 1

Confirming the Diagnosis Before Prescribing

Before prescribing any antibiotic, confirm that the patient meets at least one of three diagnostic criteria for acute bacterial rhinosinusitis (ABRS):

  • Persistent symptoms ≥ 10 days with purulent nasal discharge plus either nasal obstruction or facial pain/pressure/fullness. 2
  • Severe symptoms ≥ 3–4 consecutive days with fever ≥ 39 °C (102.2 °F), purulent nasal discharge, and facial pain. 2
  • "Double sickening": initial improvement from a viral upper respiratory infection followed by worsening symptoms within 10 days. 2

Critical context: Approximately 98–99.5% of acute rhinosinusitis cases are viral and resolve spontaneously within 7–10 days without antibiotics. 2 Do not prescribe antibiotics for symptoms lasting <10 days unless the severe criteria above are met. 2


Standard Augmentin Suspension Dosing

Tablet Formulation (Preferred)

  • Augmentin 875 mg/125 mg tablet orally twice daily for 5–7 days is the first-line regimen for otherwise healthy adults with confirmed ABRS. 3, 1

Liquid Suspension Formulation (For Adults Who Cannot Swallow Tablets)

  • Use the 125 mg/31.25 mg per 5 mL suspension in place of the 500 mg/125 mg tablet. 1
  • Dose: 28 mL of the 125 mg/31.25 mg per 5 mL suspension twice daily (equivalent to 875 mg amoxicillin/125 mg clavulanate per dose). 1
  • Alternative: The 200 mg/28.5 mg per 5 mL or 400 mg/57 mg per 5 mL suspension may be used in place of the 875 mg/125 mg tablet, though specific volume equivalents are not provided in the FDA label. 1

Important: Two 250 mg/125 mg tablets should not be substituted for one 500 mg/125 mg tablet because both contain the same amount of clavulanic acid (125 mg), making them non-equivalent. 1


Treatment Duration: 5–7 Days Is Sufficient

  • Randomized controlled trials demonstrate that a 5–7 day course of Augmentin achieves clinical cure rates of 74–80%—comparable to traditional 10-day regimens—with no difference in microbiological eradication or relapse. 3
  • Shorter courses (5–7 days) result in fewer adverse effects, particularly gastrointestinal side effects such as diarrhea. 3
  • Continue therapy for 5–7 days or until the patient is symptom-free for 7 consecutive days (typically 10–14 days total if symptoms persist beyond day 5). 3

When to Use High-Dose Augmentin (2 g/125 mg Twice Daily)

High-dose Augmentin is indicated when any of the following risk factors are present:

  • Recent antibiotic use within the past 4–6 weeks. 3
  • Age >65 years. 3
  • Daycare exposure (or close contact with daycare children). 3
  • Moderate-to-severe symptoms. 3
  • Comorbidities such as diabetes, chronic cardiac/hepatic/renal disease. 3
  • Immunocompromised state. 3
  • High local prevalence (>10%) of penicillin-resistant Streptococcus pneumoniae. 3

Rationale: The higher amoxicillin dose improves coverage of penicillin-resistant S. pneumoniae while retaining activity against β-lactamase-producing Haemophilus influenzae and Moraxella catarrhalis. 3


Monitoring and Reassessment

Early Reassessment (Day 3–5)

  • If there is no clinical improvement (persistent purulent drainage, unchanged facial pain, or worsening symptoms), switch immediately to a respiratory fluoroquinolone such as levofloxacin 500 mg once daily or moxifloxacin 400 mg once daily. 3
  • Do not extend Augmentin beyond 3–5 days without improvement; delayed escalation increases the risk of complications such as orbital cellulitis, meningitis, or intracranial abscess. 2

Day 7 Reassessment

  • Persistent or worsening symptoms should prompt confirmation of diagnosis, exclusion of complications, and consideration of imaging or ENT referral. 3

Essential Adjunctive Therapies (Add to All Patients)

  • Intranasal corticosteroids (e.g., mometasone, fluticasone, budesonide) twice daily significantly reduce mucosal inflammation and accelerate symptom resolution; supported by strong evidence from multiple randomized controlled trials. 3
  • Saline nasal irrigation 2–3 times daily provides symptomatic relief and aids mucus clearance. 3
  • Analgesics (acetaminophen or ibuprofen) for pain and fever control. 3

Watchful Waiting (Observation Without Immediate Antibiotics)

  • Initial observation without antibiotics is appropriate for adults with uncomplicated ABRS who have reliable follow-up. 3
  • Start antibiotics only if there is no improvement by day 7 or if symptoms worsen at any time. 3
  • Number needed to treat (NNT): 10–15 patients must receive antibiotics to achieve one additional cure compared with placebo, reflecting the high spontaneous recovery rate. 3

Common Adverse Effects of Augmentin

  • Diarrhea occurs in 40–43% of patients; severe diarrhea in 7–8%. 3, 4
  • Gastrointestinal adverse effects are more common with amoxicillin-clavulanate than with other antibiotics. 3
  • In comparative trials, levofloxacin was better tolerated than Augmentin, with drug-related adverse events occurring in 7.4% vs. 21.2% of patients, respectively. 5

Alternatives for Penicillin-Allergic Patients

Non-Severe (Non-Type I) Penicillin Allergy

  • Use a second- or third-generation cephalosporin (e.g., cefuroxime-axetil, cefpodoxime-proxetil, cefdinir, cefprozil) for 10 days; cross-reactivity with penicillins is negligible. 3

Severe (Type I/Anaphylactic) Penicillin Allergy

  • Use a respiratory fluoroquinolone:
    • Levofloxacin 500 mg once daily for 10–14 days, or
    • Moxifloxacin 400 mg once daily for 10 days.
  • Predicted efficacy: 90–92% against multidrug-resistant S. pneumoniae and β-lactamase-producing organisms. 3

Suboptimal Alternative

  • Doxycycline 100 mg once daily for 10 days is acceptable but has lower predicted efficacy (77–81%) and a 20–25% bacteriologic failure rate due to limited activity against H. influenzae. 3

Antibiotics to Avoid in ABRS

  • Macrolides (e.g., azithromycin): 20–25% resistance in S. pneumoniae and H. influenzae. 3
  • Trimethoprim-sulfamethoxazole: ≈50% resistance in S. pneumoniae and 27% in H. influenzae. 3
  • First-generation cephalosporins (e.g., cephalexin): ≈50% of H. influenzae strains produce β-lactamase, rendering them inadequate. 3

Referral to Otolaryngology (ENT)

Refer immediately for any of the following:

  • No improvement after 7 days of appropriate second-line antibiotic therapy. 3
  • Worsening symptoms at any point. 3
  • Suspected complications: severe headache, visual changes, periorbital swelling/erythema, proptosis, diplopia, altered mental status, or cranial nerve deficits. 3
  • Recurrent sinusitis (≥3 episodes per year) requiring evaluation for underlying allergy, immunodeficiency, or anatomic abnormality. 3

Key Pitfalls to Avoid

  • Do not extend treatment beyond 7 days without clinical justification; this raises severe diarrhea incidence (≈7–8%) without improving outcomes. 3
  • Do not prescribe antibiotics for symptoms <10 days unless severe features (fever ≥39 °C with purulent discharge for ≥3 consecutive days) are present. 3
  • Maintain a minimum 5-day course even if symptoms improve earlier, to prevent relapse and resistance development. 3
  • Avoid routine imaging (X-ray or CT) for uncomplicated ABRS; up to 87% of viral upper respiratory infections show sinus abnormalities on imaging, leading to unnecessary interventions. 3

References

Guideline

Treatment of Acute Bacterial Sinusitis

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Optimized Augmentin Therapy for Acute Bacterial Sinusitis in Adults

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Research

Comparison of the effectiveness of levofloxacin and amoxicillin-clavulanate for the treatment of acute sinusitis in adults.

Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery, 1999

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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