Adult

Delafloxacin

Warning

General Information

Fluoroquinolone

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.

For all information regarding interactions, contraception, pregnancy and breastfeeding and additional information, see BNF and Summary of Product Characteristics (SPC).

MHRA Drug Safety Updates

Fluoroquinolones, including delafloxacin are associated with disabling and potentially long-lasting or irreversible side effects. See Fluoroquinolone antibiotics - severe adverse effects

When using fluoroquinolones:

  • DO NOT prescribe for:
    • non-severe or self-limiting infections.
    • mild to moderate infections (unless other antibiotics that are commonly recommended for these infections are considered inappropriate).
  • DO read the Antimicrobial Guideline section: Fluoroquinolone antibiotics - severe adverse effects
  • DO ensure penicillin allergies are properly clarified and consider de-labelling in appropriate patients to avoid the use of fluoroquinolones. See guidelines: Penicillin allergy assessment and overview and Penicillin allergy challenge and delabelling
  • DO ensure all patients are given the MHRA fluoroquinolone patient leaflet (this is usually given to patients with their discharge and outpatient medications).

Standard dose

Intravenous: 300mg bd
Oral: 450mg bd

There is no direct evidence to support use of oral delafloxacin for the initial 3 days of a treatment course. Upon initiation of delafloxacin, intravenous therapy should be used and a switch to oral treatment can be considered after approximately 3 days. 

Obesity

No dose adjustment required.

Renal and hepatic impairment

Renal impairment

Oral:

  • No adjustment required
  • Caution in severe renal impairment - monitor renal function.
  • Not recommended in end stage renal disease

Intravenous:

eGFR (mL/min/1.73m2)

Intravenous dose

 30 or more*

Dose as in normal renal function

Less than 30*

200mg BD IV

End Stage Renal Disease (ESRD)

Not recommended by manufacturer. 

If recommended by Micro/ID discuss doses with pharmacy.

*In patients with moderate to severe renal impairment or patients with ESRD on dialysis: Accumulation of the IV vehicle sulfobutylbetadex sodium occurs therefore serum creatinine levels should be closely monitored and if creatinine increases the use of IV delafloxacin should be discussed with Micro/ID.

 

Hepatic impairment

No dose adjustment required

References

  • A. Menarini Farmaceutica Internazionale SRL. Quofenix 300 mg powder for concentrate for solution for infusion summary of product characteristics: Electronic Medicines Compendium [Internet]. Date of last revision: 22/11/23 [cited 20/1/24]. Available from: https://www.medicines.org.uk/emc/product/11481/smpc
  • A. Menarini Farmaceutica Internazionale SRL. Quofenix 450 mg tablets summary of product characteristics: Electronic Medicines Compendium [Internet]. Date of last revision: 22/11/23 [cited 20/1/24]. Available from: https://www.medicines.org.uk/emc/product/11482/smpc
  • National Institute for Health and Care Excellence (NICE). Antimicrobial prescribing: delafloxacin for acute bacterial skin and skin structure infections (ES32) [Internet]. 2021 [cited 2023 Dec 4]. Available from: https://www.nice.org.uk/advice/es32
  • Joint Formulary Committee. British National Formulary (BNF). [cited 20/1/24]. Available from: https://www.medicinescomplete.com
  • The Renal Drug Database. Delafloxacin [Internet]. Date of last revision: 31/10/23 2023 [cited  20/1/24]. Available from: https://renaldrugdatabase.com/monographs/delafloxacin
  • Melinta Therapeutics, LLC. BAXDELA- delafloxacin meglumine highlights of prescribing information: Food and Drug Administration [Internet]. 2021 [cited 2023 Dec 4]. Available from: https://nctr-crs.fda.gov/fdalabel/ui/spl-summaries/criteria/404161
  • European Medicines Agency. Quofenix European public assessment report [Internet]. 2022 [cited 2023 Dec 4]. Available from: https://www.ema.europa.eu/en/medicines/human/EPAR/quofenix
  • MHRA. Drug Safety update (January 2024) Fluoroquinolone antibiotics: must now only be prescribed when other commonly recommended antibiotics are inappropriate. Accessed HERE
  • MHRA. Drug Safety update (September 2023) Fluoroquinolone antibiotics: suicidal thoughts and behaviour. Accessed HERE
  • MHRA. Drug Safety update (August 2023) Fluoroquinolone antibiotics: reminder of the risk of disabling and potentially long-lasting or irreversible side effects. Accessed HERE
  • MHRA. Drug Safety update (December 2020) Systemic and inhaled fluoroquinolones: small risk of heart valve regurgitation; consider other therapeutic options first in patients at risk. Accessed HERE 
  • MHRA. Drug Safety update (March 2019) Fluoroquinolone antibiotics: new restrictions and precautions for use due to very rare reports of disabling and potentially long-lasting or irreversible side effects. Accessed HERE
  • MHRA. Drug Safety update (November 2018) Systemic and inhaled fluoroquinolones: small increased risk of aortic aneurysm and dissection; advice for prescribing in high-risk patients. Accessed HERE 

Editorial Information

Next review date: 01 Jun 2026

Author(s): AMST.