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.
  • 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

References

Editorial Information

Last reviewed: 23 Mar 2026

Next review date: 28 Mar 2029

Author(s): AMST.