Multivitamin

Centrum Ultra Women's

80 adverse event reports submitted to the FDA · 2010–2014 · 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 80 reports. One report may include multiple reactions — reaction totals may exceed the report count.

Choking
67
Dysphagia
33
Foreign Body Trauma
12
Throat Irritation
12
Nausea
7
Retching
7
Oesophageal Injury
4
Feeling Abnormal
3
Hypertension
3
Oropharyngeal Pain
3

Reported Outcomes

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

OutcomeReports
Other Serious or Important Medical Event 79
Hospitalization 1
Visited a Health Care Provider 1

Who Reported

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

Age

Under 18
0
18–34
1
35–49
9
50–64
7
65–79
20
80+
15
Unknown
28

52 reports had age data; 28 unknown.

Gender

Female
78
Unknown/Not Reported
2

Reports by Year

Annual report counts from 2010–2014. Spike years may reflect recalls, media coverage, or litigation rather than changes in the product.

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Hover bars for exact counts.

Context about this data: Reports concentrated in 2012 (44% of total, spanning 2010–2014), suggesting a reporting event during that period rather than evenly distributed consumer use.

← View all Centrum products in FDA data

Related Products

Centrum (348) Centrum Women Under 50 (54) Centrum Adults Under 50 (25)

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