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Cefpodoxime; Uses, Dosage, Side Effects, Interactions

Cefpodoxime is a third generation semi-synthetic cephalosporin and a beta-lactam antibiotic with bactericidal activity. Cefpodoxime’s effect is dependent on its binding to penicillin-binding proteins (PBPs) located in the bacterial cytoplasmic membrane. Binding results in the inhibition of the transpeptidase enzymes, thereby preventing cross-linking of the pentaglycine bridge with the fourth residue of the pentapeptide and interrupting consequent synthesis of peptidoglycan chains. As a result, cefpodoxime inhibits bacterial septum and cell wall synthesis formation.

Cefpodoxime is an oral third generation cephalosporin antibiotic. It is active against most Gram positive and Gram-negative bacteria. It is commonly used to treat acute otitis media, pharyngitis, and sinusitis. Cefpodoxime proxetil is a prodrug which is absorbed and de-esterified by the intestinal mucosa to Cefpodoxime.

Mechanism of action of cefpodoxime

Cefpodoxime is active against a wide spectrum of Gram-positive and Gram-negative bacteria. Cefpodoxime is stable in the presence of beta-lactamase enzymes. As a result, many organisms resistant to penicillins and cephalosporins, due to their production of beta-lactamase, may be susceptible to cefpodoxime. Cefpodoxime is inactivated by certain extended spectrum beta-lactamases. The bactericidal activity of cefpodoxime results from its inhibition of cell wall synthesis. The active metabolite of cefpodoxime binds preferentially to penicillin binding protein 3, which inhibits production of peptidoglycan, the primary constituent of bacterial cell walls.

Indications of cefpodoxime

  • For the treatment of patients with mild to moderate infections caused by susceptible strains of the designated microorganisms.
  • Bladder infection
  • Gonococcal infection,
  • Bronchitis
  • Gonococcal infection, uncomplicated
  • Skin or soft tissue infection
  • Kidney infections
  • Otitis media
  • Pneumonia
  • Sinusitis
  • Tonsillitis/pharyngitis
  • Upper respiratory tract infection
  • Acute bacterial exacerbation of chronic bronchitis
  • Acute maxillary sinusitis
  • Bacterial Infections
  • Community acquired pneumonia
  • Gonorrhea
  • Streptococcal pharyngitis
  • Streptococcal tonsillitis
  • Uncomplicated urinary uract infections
  • Uncomplicated skin and subcutaneous tissue bacterial infections

Contra-Indications of cefpodoxime

Allergies
  • Cephalosporins
  • Beta-lactams

Dosages of cefpodoxime

Strengths: 100 mg; 200 mg; 50 mg/5 mL; 100 mg/5 mL;

Bronchitis

  • Acute bacterial exacerbation of chronic bronchitis: 200 mg orally every 12 hours for 10 days

Cystitis

  • 100 mg orally every 12 hours for 7 days

Gonococcal Infection

  • Uncomplicated urethral, cervical, or female anorectal infections: 200 mg orally one time

Pneumonia

  • Community-acquired pneumonia: 200 mg orally every 12 hours for 14 days

Pyelonephritis

  • 100 mg orally every 12 hours
  • Therapy should be continued for about 14 days, depending on the nature and severity of the infection.

 Sinusitis

  • 200 mg orally every 12 hours for 10 days

Skin or Soft Tissue Infection

  • Uncomplicated infection: 400 mg orally every 12 hours for 7 to 14 days

Tonsillitis/Pharyngitis

  • 100 mg orally every 12 hours for 5 to 10 days
  • There are insufficient data to establish efficacy in the subsequent prophylaxis of rheumatic fever.

Upper Respiratory Tract Infection

  • 100 mg orally every 12 hours
  • Therapy should be continued for approximately 10 to 14 days, depending on the nature and severity of the infection.

Pediatric Dose

Bronchitis

Acute bacterial exacerbation of chronic bronchitis

  • 12 years or older: 200 mg orally every 12 hours for 10 days

Cystitis

  • 12 years or older: 100 mg orally every 12 hours for 7 days

Gonococcal Infection

Uncomplicated urethral, cervical, or female anorectal infections

  • 12 years or older: 200 mg orally one time

Side Effects of cefpodoxime

The most common

More common

Rare

Drug Interactions of cefpodoxime

Cefpodoxime may interacts with following drugs, suppliments & change the efficacy of drugs

Pregnancy & Lactation of cefpodoxime

FDA pregnancy category B

Pregnancy

Cefpodoxime proxetil was neither teratogenic nor embryocidal when administered to rats during organogenesis at doses up to 100 mg/kg/day (2 times the human dose based on mg/m²) or to rabbits at doses up to 30 mg/kg/day (1-2 times the human dose based on mg/m²).There are, however, no adequate and well-controlled studies of cefpodoxime proxetil use in pregnant women. Because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed.

Lactation

Limited information indicates that cefpodoxime produces low levels in milk and is not be expected to cause any adverse effects in breastfed infants.

References

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