Calcium Supplement

Citracal Maximum Plus

46 adverse event reports submitted to the FDA · 2018–2025 · 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 46 reports. One report may include multiple reactions — reaction totals may exceed the report count.

Choking
29
Foreign body in throat
9
Foreign body
5
Retching
3
Dysphagia
2
Pharyngeal injury
2
Abdominal distension
1
Abdominal pain upper
1
Oropharyngeal pain
1
Odynophagia
1

Reported Outcomes

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

OutcomeReports
Other Serious or Important Medical Event 41
Other Serious Outcome 8
Life Threatening 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
0
50–64
2
65–79
13
80+
10
Unknown
21

25 reports had age data; 21 unknown.

Gender

Female
32
Unknown/Not Reported
10
Male
4

Reports by Year

Annual report counts from 2018–2025. Spike years may reflect recalls, media coverage, or litigation rather than changes in the product.

'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