Anpheros Search · Treatment

Colchicine

Also known as: Colchicine Agepha Pharma · Gloperba

General information only. Anpheros does not diagnose and does not recommend treatment. Talk to a doctor or pharmacist about your situation. In an emergency, call 112 (or your local emergency number).

In short

In the European Union, colchicine is indicated for the secondary prevention of atherothrombotic events in adult patients with coronary disease that has been stable for at least 6 months. In the United States, colchicine tablets are indicated for the prophylaxis and treatment of acute gout flares, when taken at the first sign of a flare. Colchicine tablets are also indicated in the United States for the treatment of familial Mediterranean fever in adults and children four years of age or older.

From: Source: European Medicines Agency (EMA), Colchicine Agepha Pharma — EPAR, 09/09/2026. © European Medicines Agency. · Data provided by the U.S. Food and Drug Administration.

AI-generated summary of the sources cited on this page, checked automatically against them. Not reviewed by a clinician; not medical advice.

Codes

RxNorm
2683 colchicine
EMA
EMEA/H/C/006653

Official indications

Quoted unchanged from official product information, in English. Listed alphabetically by product, not ranked.

FDA (USA) Colchicine

1.1 Gout Flares Colchicine tablets are indicated for prophylaxis and the treatment of acute gout flares. • Prophylaxis of Gout Flares: Colchicine tablets are indicated for prophylaxis of gout flares. • Treatment of Gout Flares: Colchicine tablets are indicated for treatment of acute gout flares when taken at the first sign of a flare. 1.2 Familial Mediterranean Fever (FMF) Colchicine tablets are indicated in adults and children four years or older for treatment of familial Mediterranean fever (FMF).

Data provided by the U.S. Food and Drug Administration.

Document date: 20260827 · Official document →

EMA (EU) Colchicine Agepha Pharma

Colchicine AGEPHA Pharma is indicated for secondary prevention of atherothrombotic events in adult patients with coronary disease stable for at least 6 months.

Source: European Medicines Agency (EMA), Colchicine Agepha Pharma — EPAR, 09/09/2026. © European Medicines Agency.

Document date: 09/09/2026 · Official document →

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External resources

Questions

What is Colchicine approved for in the European Union?

Colchicine AGEPHA Pharma is indicated for secondary prevention of atherothrombotic events in adult patients with coronary disease stable for at least 6 months. (Source: European Medicines Agency (EMA), Colchicine Agepha Pharma — EPAR, 09/09/2026. © European Medicines Agency.)

Sources and attribution

  • Source: European Medicines Agency (EMA) — EPAR. © European Medicines Agency.
  • Data provided by the U.S. Food and Drug Administration.
  • Names other than the official source titles: Anpheros translations and plain-language names, made with AI assistance and checked automatically; the source names are in English.
  • This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.
  • Source: European Medicines Agency (EMA), Colchicine Agepha Pharma — EPAR, 09/09/2026. © European Medicines Agency.

Anpheros Search catalog 2026.10.5, published 17 October 2026. About the data →