Herbalife Supplement

Herbalife Multivitamin Complex Formula 2

35 adverse event reports submitted to the FDA · 2008–2012 · 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 35 reports. One report may include multiple reactions — reaction totals may exceed the report count.

Vomiting
9
Dizziness
6
Diarrhoea
6
Nausea
6
Pruritus
4
Abdominal Pain
4
Asthenia
4
Anxiety
4
Hypersensitivity
4
Dyspnoea
4

Reported Outcomes

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

OutcomeReports
Hospitalization 33
Visited Emergency Room 7
Visited a Health Care Provider 7
Other Serious or Important Medical Event 5
Other Serious Outcome 4
Life Threatening 1
Death 1

Who Reported

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

Age

Under 18
1
18–34
4
35–49
13
50–64
7
65–79
2
80+
0
Unknown
8

27 reports had age data; 8 unknown.

Gender

Female
27
Male
8
Unknown/Not Reported
0

Reports by Year

Annual report counts from 2008–2012. Spike years may reflect recalls, media coverage, or litigation rather than changes in the product.

'08
'09
'10
'11
'12

Hover bars for exact counts.

Context about this data: Reports concentrated in 2012 (40% of total, spanning 2008–2012), suggesting a reporting event during that period rather than evenly distributed consumer use.

← View all Herbalife products in FDA data

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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