Children's Multivitamin

Flinstones Complete

49 adverse event reports submitted to the FDA · 2008–2019 · 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 49 reports. One report may include multiple reactions — reaction totals may exceed the report count.

Drug Dependence
9
Overdose
5
Dependence
5
Suicide Attempt
2
Poisoning
2
Cough
2
Premature Baby
2
Dyspnoea
2
Bowel movement irregularity
1
Kawasaki's Disease
1

Reported Outcomes

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

OutcomeReports
Other Serious or Important Medical Event 40
Hospitalization 8
Other Serious Outcome 6
Visited Emergency Room 3
Death 2
Life Threatening 1
Other Outcome 1

Who Reported

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

Age

Under 18
13
18–34
1
35–49
3
50–64
1
65–79
0
80+
0
Unknown
31

18 reports had age data; 31 unknown.

Gender

Female
23
Male
14
Unknown/Not Reported
12

Reports by Year

Annual report counts from 2008–2019. Spike years may reflect recalls, media coverage, or litigation rather than changes in the product.

'08
'09
'10
'11
'12
'13
'14
'15
'16
'17
'18
'19

Hover bars for exact counts.

Context about this data: Reports heavily concentrated in 2012 (61% of total). High concentration may reflect a recall, enforcement action, batch filing, or litigation-driven reporting rather than ongoing consumer use.

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