Children's Multivitamin

Flintstones

78 adverse event reports submitted to the FDA · 2008–2021 · 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 78 reports. One report may include multiple reactions — reaction totals may exceed the report count.

Dependence
20
Drug Dependence
20
Choking
6
Hypersensitivity
5
Accidental overdose
3
Drug Abuser
3
Erythema
3
Haemorrhage
3
Device Dislocation
2
Dyspnoea
2

Reported Outcomes

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

OutcomeReports
Other Serious or Important Medical Event 73
Other Serious Outcome 6
Hospitalization 5
Visited a Health Care Provider 2
Visited Emergency Room 2
Death 1
Other Outcome 1

Who Reported

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

Age

Under 18
16
18–34
2
35–49
2
50–64
3
65–79
2
80+
1
Unknown
52

26 reports had age data; 52 unknown.

Gender

Female
33
Unknown/Not Reported
27
Male
18

Reports by Year

Annual report counts from 2008–2021. 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
'20
'21

Hover bars for exact counts.

Context about this data: Reports heavily concentrated in 2012 (67% 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