Each film-coated tablet contains: Febuxostat 40 mg or 80 mg.
Treatment of chronic hyperuricemia in conditions where urate deposition has already occurred.
The recommended oral dose of febuxostat is 80 mg once daily without regard to food. If serum uric acid is >6 mg/dL (357 μmol/L) after 2-4 weeks and risk factor modification has failed, febuxostat 120 mg once daily may be considered.
Hypersensitivity to the active substance or to any ingredients in drugs.
Patients being treated with azathioprine or mercaptopurine.
The safety and the efficacy of febuxostat in children below the age of 18 years have not been established. No data are available.
The most commonly reported adverse reactions and post-marketing experience are gout flares, liver function abnormalities, diarrhoea, nausea, headache, arthralgia, rash and oedema.
Mercaptopurine/azathioprine, CYP2C8 substrates, Theophylline, Naproxen or other inhibitors of glucuronidation, Inducers of glucuronidation, Colchicine/indomethacin/hydrochlorothiazide/warfarin, Desipramine/CYP2D6 substrates.
M04AA03 - febuxostat ; Belongs to the class of preparations inhibiting uric acid production. Used in the treatment of gout.
Febucid FC tab 40 mg
3 × 10's (Rp120,000/boks)
Febucid FC tab 80 mg
3 × 10's (Rp240,000/boks)