Herbalife Supplement

Herbalife Total Control

63 adverse event reports submitted to the FDA · 2004–2024 · 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 63 reports. One report may include multiple reactions — reaction totals may exceed the report count.

Nausea
12
Vomiting
11
Dyspnoea
10
Dizziness
9
Abdominal pain
9
Fatigue
8
Jaundice
8
Chest pain
7
Asthenia
7
Anxiety
6

Reported Outcomes

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

OutcomeReports
Hospitalization 49
Visited Emergency Room 20
Visited a Health Care Provider 19
Other Serious or Important Medical Event 17
Other Serious Outcome 12
Life Threatening 7
Required Intervention 1

Who Reported

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

Age

Under 18
1
18–34
21
35–49
21
50–64
6
65–79
1
80+
0
Unknown
13

50 reports had age data; 13 unknown.

Gender

Female
56
Male
6
Unknown/Not Reported
1

Reports by Year

Annual report counts from 2004–2024. Spike years may reflect recalls, media coverage, or litigation rather than changes in the product.

'04
'05
'06
'07
'08
'09
'10
'11
'12
'13
'14
'15
'16
'17
'18
'19
'20
'21
'22
'23
'24

Hover bars for exact counts.

← View all Herbalife products in FDA data

Related Products

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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