Anti-Inflammatory (Microtubule Inhibitor)
Pregnancy: Caution in first trimester (mutagenic in animal studies); limited human data suggest safe; used for FMF throughout pregnancy
Colchicine (Acute Gout)
Brand names: Colchicine (generic)
Adult dose
Dose: Acute gout: 500 mcg TDS–QDS. Or alternatively: 1 mg stat then 500 mcg after 1 hour (new UK regimen).
Route: Oral
Frequency: TDS–QDS for acute gout (max 3 days course); OD maintenance for pericarditis/familial Mediterranean fever
Max: Acute gout: 6 mg per course (do not repeat within 3 days)
Old 'until diarrhoea' regimen is no longer recommended — associated with toxicity. Low-dose regimen (1 mg + 0.5 mg at 1h) as effective as high-dose with fewer GI side effects (AGREE trial).
Paediatric dose
Route: Oral
Frequency: OD
Max: Familial Mediterranean fever (FMF): children ≥4 years: 0.5 mg OD–BD
Concentration: 500 mcg tablet mg/ml
Not used for acute gout in children. Familial Mediterranean fever: 0.5 mg OD (≥4 years). Max 1.5 mg/day in children.
Dose adjustments
Renal
Reduce dose in renal impairment: eGFR 10–50: max 1 mg per course. Avoid if eGFR <10.
Hepatic
Reduce dose in hepatic impairment — reduced clearance
Clinical pearls
- AGREE trial: 1 mg + 0.5 mg after 1h = equivalent efficacy to high-dose with 80% fewer GI side effects
- Toxicity presentations: initial GI symptoms, followed by bone marrow suppression, neuromuscular toxicity, and multi-organ failure (dose-dependent)
- Ciclosporin interaction is critical — avoid combination; if needed reduce colchicine to 0.5 mg with very careful monitoring
- COPE and ICAP trials: colchicine 500 mcg BD effective for pericarditis prevention when added to NSAIDs/aspirin
Contraindications
- Blood dyscrasias
- Severe renal AND hepatic impairment combined (increased toxicity risk)
Side effects
- Nausea, vomiting, diarrhoea (most common — dose-dependent)
- Myopathy (prolonged use or interaction with statins)
- Bone marrow suppression (rare)
- Peripheral neuropathy (rare, chronic use)
- Multi-organ failure (severe overdose)
Interactions
- Ciclosporin/tacrolimus — 5-fold increase in colchicine levels (potentially fatal)
- Statins — myopathy risk (especially simvastatin)
- Clarithromycin/erythromycin — significantly increase colchicine levels (toxicity risk)
- Verapamil/diltiazem — increase colchicine levels
Monitoring
- GI symptoms (first sign of toxicity)
- FBC (prolonged use — myelosuppression)
- Renal and hepatic function (dose adjustment)
- CK (if muscle symptoms — myopathy)
Reference: BNFc; BNF; AGREE Trial (Terkeltaub et al, Arthritis Rheum 2010); COPE/ICAP Trials; BSR Gout Guidelines. Verify against your local formulary and the latest BNF before prescribing.
Related
Curated clinical cross-links plus same-class fallbacks.
Calculators
- Murray Score for Acute Lung Injury (ALI/ARDS) · Respiratory Failure
- Simplified Acute Physiology Score 3 (SAPS 3) · ICU Scoring
- Killip Classification for Acute MI · Prognosis
- HEART Score for Major Adverse Cardiac Events · Chest Pain
- ADHERE Algorithm for Acute Decompensated Heart Failure · Risk Stratification
- Ottawa Heart Failure Risk Scale · Heart Failure
Pathways
- Falls Assessment in Older Adults · NICE CG161 2013
- Anaemia Investigation · BSH / NICE
- Lower Respiratory Tract Infection (Primary Care) · NICE NG138 / NICE antimicrobial guidance
- Hypertension Management · NICE NG136 2019
- Cutaneous Lupus Erythematosus · BAD; EULAR
- Osteoporosis / Fragility Fracture · NOGG 2021; NICE NG147; NG224