| Drug | Class | Adult | Paediatric | Notes |
|---|---|---|---|---|
| Colchicine (acute and prophylaxis)[1] | Microtubule inhibitor / anti-inflammatory | Acute: 1.2 mg PO at first symptom, then 0.6 mg 1 hour later (low-dose protocol); subsequent days 0.6 mg BD until resolution. Prophylaxis: 0.5–0.6 mg PO BD for 3–6 months at start of urate-lowering therapy | — | Renal and hepatic dose adjustment; avoid with strong CYP3A4 inhibitors (clarithromycin, ritonavir); GI side effects common |
| NSAIDs (acute)[1] | Cyclooxygenase inhibitor | Naproxen 500 mg PO BD; indomethacin 50 mg TDS; ibuprofen 800 mg TDS — until 24–48 h after attack resolves | — | First-line acute treatment in non-CKD non-cardiac patients; avoid in CKD, peptic ulcer, severe heart failure, anticoagulation; co-prescribe PPI |
| Glucocorticoid (acute)[1] | Systemic corticosteroid | Prednisolone 30–40 mg PO daily × 5 days then taper; or intra-articular methylprednisolone 40 mg in single joint | — | Useful in CKD, anticoagulation, NSAID/colchicine intolerance; intra-articular if monoarticular and septic arthritis excluded; brief course preferred |
| Allopurinol (urate-lowering)[1] | Xanthine oxidase inhibitor | Start 100 mg PO daily (50 mg if eGFR <60); titrate by 100 mg every 2–4 weeks to target serum urate <6.0; usual 300–600 mg/day, max 800 mg | 10 mg/kg/day | First-line urate-lowering; HLA-B*5801 screen in Han Chinese, Thai, Korean, South Asian; renal dose adjustment; do not stop during acute attack |
| Febuxostat (allopurinol-intolerant)[1] | Non-purine xanthine oxidase inhibitor | 40 mg PO daily start, increase to 80–120 mg if not at target | — | Allopurinol-intolerant or failure; cardiovascular event signal in CARES trial — caution in cardiovascular disease; LFT monitoring |
| Probenecid (uricosuric — selected)[1] | Uricosuric | 250 mg PO BD start, titrate to 500 mg–1 g BD | — | Add-on to xanthine oxidase inhibitor in those still above target with normal renal function and no urolithiasis history; ensure good fluid intake |
| Pegloticase (refractory tophaceous)[1] | Recombinant uricase | 8 mg IV every 2 weeks | — | Refractory tophaceous gout failing oral therapy; immunogenic — anti-drug antibodies; G6PD screen; co-prescribe immunomodulator (methotrexate) to reduce immunogenicity |
Diagnosis, acute attack management, and treat-to-target urate-lowering therapy for adults with gout.