What is the recommended dosage of cefpodoxime (Cefpodoxime proxetil) for various infections?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: December 2, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Cefpodoxime Dosing Recommendations

Cefpodoxime proxetil should be dosed at 200-400 mg orally every 12 hours for adults (depending on infection severity) and 5-10 mg/kg/dose every 12 hours for pediatric patients, with food enhancing absorption in adults but not required in children. 1

Adult Dosing by Indication

Respiratory Tract Infections

  • Community-acquired pneumonia: 200 mg every 12 hours for 14 days (total daily dose 400 mg) 1
  • Acute bacterial exacerbations of chronic bronchitis: 200 mg every 12 hours for 10 days 1
  • Acute maxillary sinusitis: 200 mg every 12 hours for 10 days 1

Upper Respiratory Infections

  • Pharyngitis/tonsillitis: 100 mg every 12 hours for 5-10 days (total daily dose 200 mg) 1

Urinary Tract Infections

  • Uncomplicated UTI: 100 mg every 12 hours for 7 days 1

Skin and Soft Tissue Infections

  • Skin and skin structure infections: 400 mg every 12 hours for 7-14 days (total daily dose 800 mg) 1

Sexually Transmitted Infections

  • Uncomplicated gonorrhea (men and women) and rectal gonococcal infections (women): 200 mg as a single dose 1

Pediatric Dosing (Ages 2 Months to 12 Years)

All pediatric dosing is based on 5 mg/kg per dose every 12 hours, with maximum doses not exceeding adult equivalents: 1

  • Acute otitis media: 5 mg/kg every 12 hours for 5 days (maximum 200 mg/dose, total daily dose 10 mg/kg up to 400 mg/day) 1
  • Pharyngitis/tonsillitis: 5 mg/kg every 12 hours for 5-10 days (maximum 100 mg/dose, total daily dose 10 mg/kg up to 200 mg/day) 1
  • Acute maxillary sinusitis: 5 mg/kg every 12 hours for 10 days (maximum 200 mg/dose, total daily dose 10 mg/kg up to 400 mg/day) 1

Special Populations

Renal Impairment

  • Severe renal impairment (creatinine clearance <30 mL/min): Extend dosing interval to every 24 hours 1
  • Hemodialysis patients: Administer dose 3 times per week after hemodialysis 1

Hepatic Impairment

  • Cirrhotic patients (with or without ascites): No dose adjustment necessary, as pharmacokinetics remain similar to healthy subjects 1

Administration Considerations

Food Effects

  • Adults and adolescents ≥12 years: Film-coated tablets should be administered with food to enhance absorption 1, 2
  • Pediatric patients 2 months to 12 years: Oral suspension may be given without regard to food 1

Drug Interactions

  • Antacids and H2-receptor antagonists: Avoid concomitant use as raising gastric pH reduces cefpodoxime absorption 2

Clinical Context and Alternative Positioning

Cefpodoxime is positioned as an alternative oral cephalosporin for β-lactamase-producing Haemophilus influenzae when amoxicillin-clavulanate cannot be used. 3 The 2011 PIDS/IDSA pediatric pneumonia guidelines list cefpodoxime alongside cefdinir, cefixime, and ceftibuten as alternatives for β-lactamase-producing H. influenzae infections 3. For pneumococcal pneumonia, cefpodoxime is listed as an alternative second- or third-generation oral cephalosporin option 3.

Important Caveats

  • Cefpodoxime is not a first-line agent for pneumococcal pneumonia; amoxicillin remains preferred for susceptible strains 3
  • For penicillin-resistant pneumococcus with high MICs, respiratory fluoroquinolones or higher-dose amoxicillin are preferred over cefpodoxime 3
  • The drug demonstrates enhanced antistaphylococcal activity compared to other oral third-generation cephalosporins like cefixime, making it useful for skin infections 4

Pharmacokinetic Properties Supporting Dosing

  • Half-life: 1.9-3.7 hours, permitting twice-daily administration 4, 2
  • Bioavailability: 50% for tablets, enhanced by food 2
  • Protein binding: Low (18-23%), facilitating tissue penetration 2
  • Excretion: Primarily renal, unchanged 5, 2

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.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.