Adult
Ertapenem
General Information
Restricted formulary antimicrobial: For details see OUH netFormulary
AWaRe antibiotic classification: 'Reserve'. All indications to be discussed with Micro/ID.
Renal and hepatic impairment
Renal impairment
eGFR (mL/min/1.73m2) |
IV dose |
More than 30 |
Dose as in normal renal function |
10-30 |
Use 50-100% of dose |
Less than 10 |
1g three times a week |
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 in hepatic impairment.
Pregnancy and breastfeeding
Pregnancy
Use only if potential benefit outweighs risk
Breastfeeding
Discuss with pharmacy.
Additional information
- There is a clinically significant interaction between carbapenems and sodium valproate or valproic acid which results in reduced valproate plasma concentrations with potential for inadequate seizure control. If patient is already prescribed sodium valproate or valproic acid and ertapenem is recommended discuss with Micro/ID and relevant medical team.
- Discuss dosing for obese patients with Micro/ID.
References
- Summary of Product Characteristics (SPC) for Invanz 1g powder for concentrate for solution for infusion. Accessed via www.medicines.org.uk 26/03/18. Last updated 15/02/16
- The Renal Drug Database. Ertapenem. Accessed via renaldrugdatabase.com 26/03/18. Last updated 19/12/17
- MHRA. Drug Safety update (December 2014). Carbapenems: concomitant use with valproic acid not recommended. Accessed at https://www.gov.uk/drug-safety-update/carbapenems-concomitant-use-with-valproic-acid-not-recommended