Drug Guide

Generic Name

Cefuroxime Axetil

Brand Names Ceftin

Classification

Therapeutic: Antibiotic, Cephalosporin

Pharmacological: Beta-lactam Antibiotic

FDA Approved Indications

  • Bacterial infections such as pneumonia, bronchitis, urinary tract infections, gonorrhea, skin infections, and otitis media

Mechanism of Action

Inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins, leading to cell lysis and death.

Dosage and Administration

Adult: 250-500 mg twice daily or 750 mg to 1.5 g once daily, depending on infection

Pediatric: 20-30 mg/kg/day divided into doses, usually twice daily

Geriatric: Dose adjustments based on renal function; caution due to potential renal impairment

Renal Impairment: Adjust dose based on creatinine clearance, typically reduced frequency or dose

Hepatic Impairment: Use with caution; no specific dose adjustment required

Pharmacokinetics

Absorption: Well absorbed from gastrointestinal tract

Distribution: Widely distributed in body tissues and fluids

Metabolism: Minimal hepatic metabolism; hydrolyzed to active metabolites

Excretion: Renal excretion of the unchanged drug and metabolites

Half Life: 1-1.2 hours

Contraindications

  • Known allergy to cefuroxime or other cephalosporins

Precautions

  • History of gastrointestinal disease, especially colitis; renal impairment; monitor for allergic reactions

Adverse Reactions - Common

  • Diarrhea (Common)
  • Nausea (Common)
  • Rash (Common)

Adverse Reactions - Serious

  • Allergic reactions including anaphylaxis (Rare)
  • Clostridioides difficile-associated diarrhea (Rare)

Drug-Drug Interactions

  • Probenecid may increase cefuroxime levels; warfarin may increase bleed risk

Drug-Food Interactions

N/A

Drug-Herb Interactions

N/A

Nursing Implications

Assessment: Monitor for allergic reactions; renal function; signs of superinfection

Diagnoses:

  • Risk for allergic reaction
  • Risk for infection
  • Impaired renal function

Implementation: Administer with food to improve absorption; monitor renal function during therapy

Evaluation: Assess resolution of infection symptoms; monitor for adverse reactions

Patient/Family Teaching

  • Complete the full course of therapy.
  • Report signs of allergic reaction immediately.
  • Take with food to reduce gastrointestinal upset.

Special Considerations

Black Box Warnings:

  • Hypersensitivity reactions in patients allergic to penicillins or other beta-lactams

Genetic Factors: None specified

Lab Test Interference: May cause false-positive Coombs test

Overdose Management

Signs/Symptoms: Diarrhea, nausea, vomiting, gastrointestinal upset

Treatment: Supportive care; hemodialysis may be considered in severe cases

Storage and Handling

Storage: Store at room temperature, 20-25°C (68-77°F)

Stability: Stable for the duration of the expiration date when stored properly

This guide is for educational purposes only and is not intended for clinical use.