Adult
Nitrofurantoin
Warning
General Information
Nitrofuran antibiotic
Immediate release preparations: Formulary antimicrobial: Use in accordance with Trust guidelines.
- OUH only stocks immediate release preparations
- Modified release preparations are Non-formulary. See the Therapeutic Substitution Medicines Information Leaflet.
AWaRe antibiotic classification: 'Access'. Use as per guidelines.
For all information regarding interactions, contraception, pregnancy and breastfeeding and additional information, see BNF and Summary of Product Characteristics (SPC).
Standard dose
|
Oral dose |
|
| Standard dose |
50mg QDS |
Renal and hepatic impairment
Renal impairment
- Check renal function before starting nitrofurantoin, especially in the elderly.
- The antibacterial efficacy of nitrofurantoin depends on adequate renal secretion into the urinary tract. Therefore, there is reduced efficacy of nitrofurantoin in renal impairment.
- Avoid if eGFR less than 45mL/min/1.73m2.
- A short course (3-7 days) may be used with caution in patients with an eGFR between 30-44mL/min/1.73m2 to treat resistant pathogens, when the benefits of nitrofurantoin may outweigh the risks.
- For more information see MHRA Drug Safety Update (February 2015) Nitrofurantoin now contraindicated in most patients with an estimated glomerular filtration rate (eGFR) of less than 45 ml/min/1.73m2[LD1]
- HD/HDF/High Flux/PD: Contra-indicated.
Hepatic impairment
Use with caution. No dose adjustment required.
- Hepatic reactions including cholestatic jaundice, autoimmune hepatitis and chronic active hepatitis and hepatic necrosis have been reported with the use of nitrofurantoin.
- Be vigilant for symptoms and signs of liver dysfunction in patients taking nitrofurantoin for any duration, but particularly with long-term use, and monitor patients periodically for signs of hepatitis and for changes in biochemical tests that would indicate hepatitis or liver injury.
- For more information see MHRA Drug Safety Update (April 2023) Nitrofurantoin: reminder of the risks of pulmonary and hepatic adverse drug reactions
MHRA Drug Safety Updates
MHRA Drug Safety Update (February 2015):
MHRA Drug Safety Update (April 2023):
Nitrofurantoin: reminder of the risks of pulmonary and hepatic adverse drug reactions
References
- ADVANZ Pharma. Nitrofurantoin 50mg Capsules summary of product characteristics. Electronic Medicines Compendium. Last revision of the text 08/25 Available from: https://www.medicines.org.uk Accessed 23/3/26.
- The Renal Drug Database. Nitrofurantoin. Last updated 21/11/24 Available from: https://www.renaldrugdatabase.com Accessed 23/3/26
- British National Formulary. Nitrofurantoin. BNF online accessed via www.medicinescomplete.com Accessed 23/3/26.
- Sanford guide [online]. Nitrofurantoin. Last updated 13/3/26. Accessed via https://webedition.sanfordguide.com Accessed 23/3/26
- MHRA. Drug Safety Update (February 2015). Nitrofurantoin now contraindicated in most patients with an estimated glomerular filtration rate (eGFR) of less than 45 ml/min/1.73m2 Accessed via https://www.gov.uk/drug-safety-update/nitrofurantoin-now-contraindicated-in-most-patients-with-an-estimated-glomerular-filtration-rate-egfr-of-less-than-45-ml-min-1-73m2 Accessed 23/3/26
- MHRA. Drug Safety Update (April 2023) Nitrofurantoin: reminder of the risks of pulmonary and hepatic adverse drug reactions Accessed via https://www.gov.uk/drug-safety-update/nitrofurantoin-reminder-of-the-risks-of-pulmonary-and-hepatic-adverse-drug-reactions Accessed 23/3/26