The FDA Adverse Event Reporting System (FAERS) collects post-marketing safety reports, but such spontaneous reporting systems have inherent limitations and cannot establish causation or absence of risk
Abstract Hyperuricemia, characterized by elevated levels of serum uric acid (SUA), is linked to a spectrum of commodities such as gout, cardiovascular diseases, renal disorders, metabolic syndrome, and diabetes, etc
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Over the past 10 years, it has emerged from multiple drug screens as a very interesting compound
Human clinical trials remain limited, and claims of guaranteed outcomes should be treated with appropriate skepticism
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