Multivitamin

Centrum Silver Women's 50+

1,415 adverse event reports submitted to the FDA · 2011–2025 · 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 1,415 reports. One report may include multiple reactions — reaction totals may exceed the report count.

Choking

962

Dysphagia

524

Foreign Body Trauma

206

Throat irritation

118

Retching

Foreign body

Dyspnoea

Vomiting

Oropharyngeal pain

Coeliac disease

Reported Outcomes

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

Outcome	Reports
Other Serious or Important Medical Event	1,308
Hospitalization	102
Visited a Health Care Provider	49
Other Serious Outcome	25
Visited Emergency Room	17
Death	12
Other Outcome	12
Life Threatening	4
Disability	3

Who Reported

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

Age

Under 18

18–34

35–49

50–64

117

65–79

340

80+

347

Unknown

596

819 reports had age data; 596 unknown.

Gender

Female

1,334

Unknown/Not Reported

Male

Reports by Year

Annual report counts from 2011–2025. 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