Brand Family

Centrum Products in FDA Data

Individual FDA adverse event report counts for Centrum 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.

Centrum Product Variants

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

Centrum 348 reports · 2007–2025
Centrum Ultra Women's 80 reports · 2010–2014
Centrum Women Under 50 54 reports · 2012–2024
Centrum Adults Under 50 25 reports · 2012–2020

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