Multivitamin

Centrum Silver Women's 50+

1,495 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 1,495 reports. One report may include multiple reactions — reaction totals may exceed the report count.

Choking

1,015

Dysphagia

557

Foreign Body Trauma

216

Throat irritation

122

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	1,385
Hospitalization	106
Visited a Health Care Provider	50
Other Serious Outcome	25
Visited Emergency Room	17
Death	13
Other Outcome	12
Disability	4
Life Threatening	4

Who Reported

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

Age

Under 18

18–34

35–49

50–64

120

65–79

359

80+

366

Unknown

635

860 reports had age data; 635 unknown.

Gender

Female

1,409

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.

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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.

Explore raw FDA reports for this product ↗

Raw query results may differ from page counts — this page applies name normalization across product variants. About our methodology · How to read this data