Increased Death Risk Prompts Boxed Warning for Gout Drug

Doctors should avoid prescribing the popular gout drug Uloric (febuxostat) in favor of Zyloprim (allopurinol) since there is an increased risk of death associated with Uloric, according to an FDA warning.

The FDA says its review of a postmarket trial of 6,000 patients comparing Uloric to Zyloprim found that Uloric was associated with an increased risk of heart-related death, as well as deaths from other causes, compared to Zyloprim. The analysis showed that there were 15 deaths per 1,000 people from heart-related causes for those in Uloric compared to 11 per 1,000 on Zyloprim.

As a result, the agency is requiring that the drug’s label contain a “black box” warning – the FDA’s most severe – warning of this risk. The FDA added that Uloric should be reserved for patients who fail on or who can’t tolerate Zyloprim. This essentially relegated Uloric to a second-line treatment.

Last year, consumer advocacy group Public Citizen urged the FDA to pull Uloric from the market. Uloric is also known to cause joint and muscle pain, as well as nausea.


Jonathan Block

Jonathan Block

Jonathan Block is an associate editor at BioCentury, which provides news and information about the biotechnology and pharmaceutical industries. Prior to joining BioCentury in 2019, Jonathan worked for MedShadow as content editor. He has been an editor and writer for multiple pharmaceutical, health and medical publications, including The Pink Sheet, Modern Healthcare, Health Plan Week and Psychiatry Advisor. He holds a BA from Tufts University and is earning an MPH with a focus on health policy from the CUNY Graduate School of Public Health & Health Policy.


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