Colchicine (Colcrys/Mitigare)

Metabolicprescriptionoral · inferred

Microtubule polymerization inhibitor (tubulin binder) with anti-inflammatory activity, used for acute and prophylactic gout, familial Mediterranean fever, pericarditis, and, at low dose, secondary cardiovascular prevention (LoDoCo2). Typical regimens: 1.2 mg then 0.6 mg one hour later for acute gout flare (max 1.8 mg day 1), 0.6 mg BID for gout prophylaxis, 0.5 mg QD for cardiovascular maintenance. Plasma half-life ~20-40h. Oral bioavailability ~45%. Substrate of CYP3A4 and P-glycoprotein, NARROW THERAPEUTIC WINDOW with life-threatening toxicity (multi-organ failure, pancytopenia, rhabdomyolysis) when co-administered with strong CYP3A4 inhibitors (clarithromycin, ritonavir, ketoconazole, verapamil, diltiazem, grapefruit). Contraindicated in severe renal/hepatic impairment with interacting drugs.

Projected serum levels — 0.60 mg, once daily

Colchicine (Colcrys/Mitigare)
Colchicine (Colcrys/Mitigare) modeled serum levels, 0.60 mg once daily over 15 days Population-based pharmacokinetic estimate. Steady state reached after approximately 3 days. 0 0.25 0.50 0.75 1 Day 0 Day 4 Day 8 Day 11 Day 15 Time on a regular schedule ≈ steady state · day 3
Colchicine (Colcrys/Mitigare) modeled serum levels with a loading dose of 1.3 mg, then 0.60 mg once daily The first dose is larger so levels approach steady state faster. 0 0.25 0.50 0.75 1 Day 0 Day 4 Day 8 Day 11 Day 15 Time on a regular schedule

Maintenance schedule: 0.60 mg once daily (oral).

Loading schedule: 1.3 mg on day 1, then 0.60 mg once daily — reaching therapeutic levels sooner.

Modeled steady state after ~3 days: peak ≈ 0.55 mg, trough ≈ 0.30 mg body load. Population-based estimate over 15 days for a 0.60 mg dose at a 70 kg reference body mass — the interactive app scales curves to your doses, timing, and body mass.

Key facts

Category
Metabolic
Route modeled
Oral
Model confidence
inferred
Half-life
27 h
Common dose
0.60 mg
Suggested maximum
1.8 mg/day
Reference dose range
0.30–1.8 mg (single dose)
Suggested cadence
once daily
Validated against
0.60 mg oral — Cmax 0.003 mg/L at 1.3 h

Documented interactions

  • contraindicated
    Carbamazepine (Tegretol) + Colchicine (Colcrys/Mitigare) CYP induction

    Carbamazepine (Tegretol) inducer of CYP3A4 predicted to change Colchicine (Colcrys/Mitigare) AUC by ~0.20x

  • contraindicated
    Clarithromycin (Biaxin) + Colchicine (Colcrys/Mitigare) CYP inhibition

    Clarithromycin (Biaxin) mechanism_based of CYP3A4 predicted to change Colchicine (Colcrys/Mitigare) AUC by ~10.00x

  • contraindicated
    Dasatinib (Sprycel) + Colchicine (Colcrys/Mitigare) CYP inhibition

    Dasatinib (Sprycel) time_dependent_inhibitor of CYP3A4 predicted to change Colchicine (Colcrys/Mitigare) AUC by ~5.00x

  • contraindicated
    Diltiazem + Colchicine (Colcrys/Mitigare) CYP inhibition

    Diltiazem mechanism_based of CYP3A4 predicted to change Colchicine (Colcrys/Mitigare) AUC by ~10.00x

  • contraindicated
    Efavirenz (Sustiva) + Colchicine (Colcrys/Mitigare) CYP induction

    Efavirenz (Sustiva) inducer of CYP3A4 predicted to change Colchicine (Colcrys/Mitigare) AUC by ~0.12x

  • contraindicated
    Grapefruit (whole fruit) + Colchicine (Colcrys/Mitigare) CYP inhibition

    Grapefruit (whole fruit) mechanism_based of CYP3A4 predicted to change Colchicine (Colcrys/Mitigare) AUC by ~10.00x

Serum checks 61 modeled interaction pairings for colchicine (colcrys/mitigare) across your whole stack — absorption conflicts, enzyme inhibition, and nutrient depletion included.

Research behind this entry

  1. Colchicine update: 2008 Terkeltaub RA · Clinical Pharmacokinetics, 2009 DOI

    Comprehensive PK/clinical review establishing colchicine t1/2 20-40h, F~45%, CYP3A4 and P-gp metabolism, and narrow therapeutic index with life-threatening toxicity when combined with CYP3A4 inhibitors.

  2. Colchicine in patients with chronic coronary disease (LoDoCo2) Nidorf SM et al. · New England Journal of Medicine, 2020 DOI

    Pivotal 5522-patient RCT showing low-dose colchicine 0.5 mg QD reduced major adverse cardiovascular events by 31% vs placebo in chronic coronary disease, established CV prevention indication.

2 published studies referenced in the app, each with a plain-language summary.