Multivitamin

Centrum Silver

809 adverse event reports submitted to the FDA · 2004–2025 · 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 809 reports. One report may include multiple reactions — reaction totals may exceed the report count.

Choking

238

Dysphagia

130

Coeliac disease

Foreign Body Trauma

Nausea

Diarrhoea

Abdominal pain upper

Malaise

Dyspnoea

Weight decreased

Reported Outcomes

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

Outcome	Reports
Other Serious or Important Medical Event	697
Hospitalization	102
Visited a Health Care Provider	95
Other Serious Outcome	46
Visited Emergency Room	46
Death	23
Other Outcome	16
Disability	12
Life Threatening	12
Required Intervention	4
Allergic Reaction	1

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

215

80+

154

Unknown

331

478 reports had age data; 331 unknown.

Gender

Female

562

Male

210

Unknown/Not Reported

Reports by Year

Annual report counts from 2004–2025. 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