Brand Family

Super Beta Products in FDA Data

Individual FDA adverse event report counts for Super Beta product variants. Counts are per-product — they are never combined across SKUs.

These are reports submitted to the FDA. A report does not mean any product caused the effect. Each SKU's count is tracked individually and is never summed across variants.

Super Beta Product Variants

Each entry is a distinct product as named in FDA reports. Click any product to see its full adverse event breakdown.

Super Beta Prostate 1,108 reports · 2012–2021
Super Beta Prostate P3 Advanced 240 reports · 2017–2021
Super Beta Virility Boost 145 reports · 2016–2019

Data Source

Data from FDA's CFSAN Adverse Event Reporting System (CAERS). Reports are voluntary submissions — they do not establish that any product caused any event.

View openFDA CAERS source ↗ · About our methodology