Flucloxacillin
Penicillin · Antibiotic
Also known as Flucloxacillin sodium
Mechanism
Flucloxacillin is an isoxazolyl penicillin that inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs) and blocking transpeptidation of peptidoglycan. The isoxazolyl side chain provides steric protection of the beta-lactam ring from hydrolysis by staphylococcal penicillinases, conferring narrow-spectrum activity primarily against penicillinase-producing Staphylococcus aureus. It is associated with a pharmacogenomic risk of drug-induced liver injury linked to the HLA-B*57:01 allele.
Indications
Dosing
- Hepatic adjustment
- Use with caution in patients with hepatic impairment; increased risk of cholestatic jaundice and hepatitis with increasing age and administration for more than 2 weeks.
Contraindications
- Penicillin allergy
- History of hepatic dysfunction associated with flucloxacillin
Side effects
- Cholestatic jaundice
- Hepatitis
- Erythematous rashes (increased risk in acute lymphocytic leukaemia and chronic lymphocytic leukaemia)
- Hypersensitivity reactions (rash to anaphylaxis)
- Serum sickness
- Stevens-Johnson syndrome
- Nephropathy
- Hematologic reactions (neutropenia, prolonged use)
- Neurotoxicity (seizure, high doses, renal impairment)
Drug interactions
1 additional unreviewed or low-confidence interaction hidden because their provenance or source detail is insufficient.
Related guidelines
Other Penicillin drugs
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Textbook-sourced·Sources: Harrison 22e, Katzung, BNF·Updated: 2026-05-10