Benzbromarone

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Information about Benzbromarone[edit source]

Benzbromarone is a nonpurine xanthine oxidase inhibitor used for the treatment of gout, but never approved for use in the United States because of concerns over reports of acute liver injury and deaths with its use.

Mechanism of action of Benzbromarone[edit source]

Benzbromarone (benz broe' ma rone) is a nonpurine inhibitor of xanthine oxidase that shares no structural homology to allopurinol or to hypoxanthine, but rather is a structural homologue of amiodarone and dronedarone. Therapy leads to lowering of serum uric acid levels within a few weeks, and chronic therapy has been shown to decrease uric acid levels into target levels of less than 6 mg/dL and to decrease acute gouty attacks.

FDA approval information for Benzbromarone[edit source]

Benzbromarone was approved for use in Europe and Asia, but was not licensed in the United States because of concerns over hepatotoxicity.

Withdrawn[edit | edit source]

Benzbromarone was withdrawn by its sponsor in 2003 because of continuing concerns over hepatotoxicity.

The following drugs are considered antigout medications:

Benzbromarone Resources
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Contributors: Prab R. Tumpati, MD