Adult

Cefuroxime

Warning

General Information

 Do NOT use if patient has a history of severe penicillin allergy.  If in doubt, discuss with Micro/ID.

Restricted formulary antimicrobial: For details see OUH netFormulary

AWaRe antibiotic classification: 'Watch'. Use as per guidelines. All other indications to be discussed with Micro/ID.

Renal and hepatic impairment

Renal impairment

eGFR (mL/min/1.73m2)

IV Dose

More than 20

Dose as in normal renal function

10-20

750mg-1.5g every 12 hours

Less than 10

750mg-1.5g every 24 hours

HD/HDF/High Flux/PD

Dose as in eGFR less than 10ml/min/1.73m2.

Dialysed; give after dialysis

 

Hepatic impairment
No dose adjustment required

Pregnancy and breastfeeding

Pregnancy

Not known to be harmful

Breastfeeding

Present in milk in low concentration but appropriate to use

Additional information

Only IV cefuroxime is on the OUHFT Formulary.

References

  1. Summary of Product Characteristics (SPC) for Cefuroxime 1.5g Powder for solution for Injection or Infusion. Accessed via www.medicines.org.uk 26/03/18. Last updated 13/06/14
  2. The Renal Drug Database. Cefuroxime. Accessed via renaldrugdatabase.com 26/03/18. Last updated 21/12/17
  3. Drugs in Pregnancy and Lactation. Briggs G et al. 6th Edition.

Editorial Information

Next review date: 02 Mar 2026