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Febuxostat

ULORIC

Pronunciation: feb-UX-oe-stat (yoo-LOR-ik)

Febuxostat ballicule: receptor binding, kinetics and half-life diagram
Mechanism of action: Febuxostat ballicule

What it isNon-purine xanthine oxidase inhibitor; chronic urate lowering in gout.

Why this oneIts non-purine structure makes it an option after allopurinol intolerance or hypersensitivity.

What limits itA cardiovascular-death signal keeps it second-line; xanthine oxidase inhibition can dangerously raise azathioprine or mercaptopurine.

Febuxostat molecular structure (skeletal formula)
Molecular structure: Febuxostat

FDA-approved for

FDA label

BOXED WARNING Cardiovascular death: higher rate of CV death vs allopurinol in gout patients with established CV disease; use only in patients with inadequate response/intolerance to allopurinol or for whom allopurinol is not advisable
FDA dosingPopulationStartTargetMax
Chronic gout (hyperuricemia)Adults40 mg QD80 mg QD if sUA ≥6 mg/dL after 2 wk80 mg QD

Titration Increase to 80 mg QD if serum uric acid ≥6 mg/dL after 2 weeks

Renal Mild–moderate: no adjustment; severe (CrCl 15–29): limit to 40 mg QD

Hepatic No adjustment for mild–moderate (Child-Pugh A/B); severe (C) not studied — use caution

Instructions

Available strengths

Contraindications

Cautions

Adverse reactions

Pregnancy Limited data insufficient to inform risk; no adverse developmental effects in animal studies at exposures up to ~40–51x MRHD

Lactation No human data; present in rat milk

Cost

Febuxostat (ULORIC)
What pharmacies pay · NADAC 9/30/26
Strength#/mogeneric $/moCostPlus
40 mgtab30 qd$5.73offered
80 mgtab30 qd$7.83offered

Generic entry2019

⚠ BOXED WARNING

Principal riskCardiovascular death signal versus allopurinol

Classes and tags

Clinical profile

Therapeutic safety burden2 / 4
Overdose danger1 / 4
Weight-gain liability0 / 4
Sedation liability0 / 4
QT / Torsades0 / 4
Direct muscarinic antagonism0 / 4
Embryofetal risk2 / 4

Legacy pregnancy categoryC

Defining liabilityGenerally tolerated at therapeutic doses; clinically important risks are agent-specific and increase with interactions or organ impairment.

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