Multivitamin

Centrum Silver Adults 50+

325 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 325 reports. One report may include multiple reactions — reaction totals may exceed the report count.

Choking

144

Dysphagia

Foreign body

Foreign Body Trauma

Throat irritation

Malaise

Retching

Weight decreased

Cough

Dyspnoea

Reported Outcomes

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

Outcome	Reports
Other Serious or Important Medical Event	286
Hospitalization	40
Visited a Health Care Provider	26
Other Serious Outcome	12
Death	7
Disability	4
Other Outcome	3
Visited Emergency Room	3
Life Threatening	2
Required Intervention	2
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

80+

Unknown

139

186 reports had age data; 139 unknown.

Gender

Female

208

Male

102

Unknown/Not Reported

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