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Uricosuric Agent — Potent URAT1 Inhibitor

Benzbromarone

Brand names: Desuric (not UK licensed — available via MHRA named patient basis)

Benzbromarone is a potent uricosuric agent used to lower serum urate in gout, generally where other urate-lowering therapies are unsuitable or ineffective.

Dosing — being independently re-sourced

ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.

Clinical monograph

How it works

It inhibits the URAT1 transporter in the proximal renal tubule, reducing reabsorption of uric acid and thereby increasing its urinary excretion.

Prescribing in practice

  • It has been associated with rare but serious hepatotoxicity, so liver function must be monitored and the drug is reserved for selected patients under specialist guidance.
  • It is not licensed in the UK and is used only on a named-patient or unlicensed basis where appropriate.
  • Increasing urinary urate can precipitate urate stones; adequate fluid intake and urine alkalinisation may be advised, and it is less effective in significant renal impairment.

Monitoring

Monitor liver function periodically, particularly in the early months of treatment, alongside serum urate and renal function.

Counselling the patient

  • Maintain a good fluid intake throughout treatment.
  • Report yellowing of the skin or eyes, dark urine or persistent nausea, which may indicate liver problems.
  • An acute flare of gout may occur when starting; do not stop treatment without advice.

Evidence & guidelines

Its uricosuric efficacy is well described in the gout literature, though use is limited by hepatotoxicity concerns and lack of UK licensing.

Reference: BSR Gout Guidelines 2017; NICE NG219; EULAR Gout Guidelines 2016; MHRA Named Patient Guidance; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.