Delafloxacin
General Information
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 contra-indications, 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