Calcium Supplement

Citracal Maximum Cholecalciferol + Calcium Citrate

33 adverse event reports submitted to the FDA · 2012–2015 · 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 33 reports. One report may include multiple reactions — reaction totals may exceed the report count.

Choking

Foreign Body

Foreign Body Trauma

Oropharyngeal Pain

Dysphagia

Retching

Coeliac Disease

Oesophageal Injury

Throat Irritation

Dyspnoea

Reported Outcomes

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

Outcome	Reports
Other Serious or Important Medical Event	32
Hospitalization	2

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

26 reports had age data; 7 unknown.

Gender

Female

Male

Unknown/Not Reported

Reports by Year

Annual report counts from 2012–2015. Spike years may reflect recalls, media coverage, or litigation rather than changes in the product.

'12

'13

'14

'15

Hover bars for exact counts.

Context about this data: Reports concentrated in 2015 (46% of total, spanning 2012–2015), suggesting a reporting event during that period rather than evenly distributed consumer use.

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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.

View openFDA CAERS data ↗ · About our methodology · How to read this data