Multivitamin

Centrum Silver Men's 50+

306 adverse event reports submitted to the FDA · 2012–2025 · Data current as of June 3, 2026

These are reports submitted to the FDA. A report does not mean the product caused the effect. Counts reflect reporting activity, not how common an effect is.

Most Reported Reactions

Top 10 reactions from 306 reports. One report may include multiple reactions — reaction totals may exceed the report count.

Choking

Dysphagia

Foreign body

Foreign body in throat

Coeliac disease

Cough

Neuropathy peripheral

Myocardial infarction

Cerebrovascular accident

Vitamin B6 increased

Reported Outcomes

Outcome categories as recorded in FDA reports. One report may include multiple outcomes.

Outcome	Reports
Other Serious or Important Medical Event	253
Hospitalization	41
Visited a Health Care Provider	33
Other Serious Outcome	21
Death	12
Visited Emergency Room	7
Other Outcome	4
Life Threatening	3
Disability	2

Who Reported

Reporter demographics where available. Many reports do not include age or gender data.

Age

Under 18

18–34

35–49

50–64

65–79

80+

Unknown

154

152 reports had age data; 154 unknown.

Gender

Unknown/Not Reported

Male

259

Female

Reports by Year

Annual report counts from 2012–2025. Spike years may reflect recalls, media coverage, or litigation rather than changes in the product.

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Hover bars for exact counts.

← View all Centrum Silver products in FDA data

Data Source

This page presents data from the FDA's CFSAN Adverse Event Reporting System (CAERS) via the openFDA API. Reports are voluntary and unverified. The FDA has not concluded that this product caused any reported event.

View openFDA CAERS data ↗ · About our methodology · How to read this data