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Antibiotic (2nd Generation Cephalosporin) Pregnancy: Limited data in pregnant women; animal studies show no reproductive toxicity. Should be prescribed to pregnant women only if benefit outweighs risk. Crosses the placenta. Excreted in breast milk in small quantities.

Cefuroxime

Brand names: Zinnat (oral), Zinacef (IV)

Cefuroxime is a second-generation cephalosporin available in intravenous and oral forms, used for respiratory, urinary, skin, and soft-tissue infections and widely as surgical antibiotic prophylaxis.

Auto-extracted from the source labelling — not yet independently clinician-verified. These values were distilled from the UK SPC (or the US label where noted) but have not had a clinician sign-off. Confirm against the current SmPC before prescribing.

Adult dose

Dose: 750 mg to 1.5 g
Route: intravenous or intramuscular injection
Frequency: every 8 hours
Dose depends on indication (parenteral cefuroxime sodium, adults/children >=40 kg): community-acquired pneumonia and acute exacerbations of chronic bronchitis 750 mg every 8 h; soft-tissue infections (cellulitis, erysipelas, wound infections), intra-abdominal infections, complicated UTI including pyelonephritis 1.5 g every 8 h; severe infections 750 mg every 6 h IV or 1.5 g every 8 h IV. Surgical prophylaxis (GI, gynaecological incl. caesarean, orthopaedic): 1.5 g at induction of anaesthesia, optionally supplemented by two 750 mg IM doses after 8 h and 16 h; cardiovascular/oesophageal operations: 1.5 g at induction then 750 mg IM every 8 h for a further 24 h. Method: IV over 3-5 min or deep IM (max 750 mg per IM site); doses >1.5 g must be given IV. PAEDIATRIC (children <40 kg, per source): 30-100 mg/kg/day IV in 3-4 divided doses (60 mg/kg/day appropriate for most infections); infants birth to 3 weeks 30-100 mg/kg/day IV in 2-3 divided doses. Verify paediatric dosing against a children's formulary.

Dose adjustments

Renal

Reduce dose in markedly impaired renal function. CrCl >20 mL/min/1.73m2: no reduction of standard dose (750 mg-1.5 g three times daily). CrCl 10-20 mL/min/1.73m2: 750 mg twice daily. CrCl <10 mL/min/1.73m2: 750 mg once daily. Haemodialysis: a further 750 mg IV/IM at the end of each dialysis (peritoneal dialysis: 250 mg per 2 L dialysis fluid). CAVH/high-flux haemofiltration: 750 mg twice daily.

Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.

Contraindications

  • Hypersensitivity to cefuroxime or to any of the cephalosporins
  • Previous immediate and/or severe hypersensitivity (e.g. anaphylactic reaction) to any other type of beta-lactam antibacterial (penicillins, monobactams and carbapenems)

Side effects

  • Neutropenia, eosinophilia
  • Transient rise in liver enzymes or bilirubin
  • Injection site reactions (pain, thrombophlebitis)
  • Skin rash, urticaria and pruritus
  • Gastrointestinal disturbance; Candida overgrowth; pseudomembranous colitis (uncommon)

Interactions

  • Potent diuretics (e.g. furosemide) — cephalosporins at high dosage should be given with caution; renal impairment reported
  • Aminoglycosides — caution with concurrent use; renal impairment reported; do not mix in the same solution

Clinical monograph

How it works

It inhibits bacterial cell wall synthesis by binding penicillin-binding proteins and has useful stability against some beta-lactamases.

Prescribing in practice

  • Avoid in patients with a history of severe or anaphylactic reaction to penicillins or cephalosporins because of cross-reactivity risk.
  • When used for surgical prophylaxis it should be given so that adequate tissue concentrations are present at the time of incision, with re-dosing for prolonged procedures or major blood loss.
  • Adjust dosing in renal impairment, and be alert to antibiotic-associated diarrhoea and Clostridioides difficile infection.

Monitoring

Monitor for hypersensitivity, clinical response, renal function where relevant, and signs of antibiotic-associated diarrhoea.

Counselling the patient

  • Take the oral tablets with food to improve absorption and complete the prescribed course.
  • Report any rash, swelling, or breathing difficulty straight away.
  • Tell your doctor if you develop severe or persistent diarrhoea.

Evidence & guidelines

Cefuroxime is an established cephalosporin with well-documented efficacy in common infections and as surgical prophylaxis in NICE and stewardship guidance.

Reference: WHO Surgical Site Infection Prevention Guidelines; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.