Calcium Supplement

Citracal Slow Release 1200

62 adverse event reports submitted to the FDA · 2017–2025 · 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 62 reports. One report may include multiple reactions — reaction totals may exceed the report count.

Choking
36
Foreign body
14
Foreign body in throat
12
Retching
3
Nephrolithiasis
3
Throat irritation
2
Oropharyngeal pain
2
Vomiting
2
Odynophagia
2
Choking sensation
1

Reported Outcomes

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

OutcomeReports
Other Serious or Important Medical Event 52
Other Serious Outcome 18
Life Threatening 3
Hospitalization 2

Who Reported

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

Age

Under 18
0
18–34
0
35–49
2
50–64
4
65–79
19
80+
13
Unknown
24

38 reports had age data; 24 unknown.

Gender

Female
46
Unknown/Not Reported
14
Male
2

Reports by Year

Annual report counts from 2017–2025. Spike years may reflect recalls, media coverage, or litigation rather than changes in the product.

'17
'18
'19
'20
'21
'22
'23
'24
'25

Hover bars for exact counts.

← View all Citracal products in FDA data

Related Products

Citracal Maximum (592) Citracal Petites (416) Citracal (89)

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