Calcium Supplement

Citracal

89 adverse event reports submitted to the FDA · 2008–2025 · 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 89 reports. One report may include multiple reactions — reaction totals may exceed the report count.

Choking

Foreign body

Dysphagia

Dyspnoea

Foreign Body Trauma

Retching

Diarrhoea

Throat irritation

Vomiting

Malaise

Reported Outcomes

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

Outcome	Reports
Other Serious or Important Medical Event	71
Other Serious Outcome	15
Visited a Health Care Provider	10
Hospitalization	10
Visited Emergency Room	9
Other Outcome	3
Death	2
Disability	2
Required Intervention	1
Allergic Reaction	1
Life Threatening	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

55 reports had age data; 34 unknown.

Gender

Female

Unknown/Not Reported

Male

Reports by Year

Annual report counts from 2008–2025. Spike years may reflect recalls, media coverage, or litigation rather than changes in the product.

'08

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'22

'23

'24

'25

Hover bars for exact counts.

← View all Citracal 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