| Drug | Class | Adult | Paediatric | Notes |
|---|---|---|---|---|
| Colchicine (low-dose)[1] | Microtubule inhibitor / anti-inflammatory | Acute: 1.0 mg PO at first symptom, then 0.5 mg 1 hour later; subsequent days 0.5 mg BD until resolution. Prophylaxis: 0.5 mg PO BD for 3–6 months at start of urate-lowering therapy | — | Renal and hepatic dose adjustment; avoid with strong CYP3A4 inhibitors; 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; 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 |
| 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 recommended before initiation in South Asian populations; renal dose adjustment |
| 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 — caution in cardiovascular disease; LFT monitoring |
Diagnosis, acute attack management, and treat-to-target urate-lowering therapy for adults with gout per Indian Rheumatology Association guidance.