Wellness Supplement

Plexus Probio 5

34 adverse event reports submitted to the FDA · 2014–2024 · 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 34 reports. One report may include multiple reactions — reaction totals may exceed the report count.

Diarrhoea
9
Abdominal pain upper
6
Vomiting
6
Abdominal pain
6
Dyspnoea
6
Chest pain
5
Nausea
5
Abdominal distension
4
Pyrexia
3
Urticaria
3

Reported Outcomes

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

OutcomeReports
Hospitalization 26
Other Serious or Important Medical Event 9
Visited a Health Care Provider 6
Visited Emergency Room 4
Allergic Reaction 2
Other Serious Outcome 2

Who Reported

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

Age

Under 18
0
18–34
1
35–49
3
50–64
5
65–79
3
80+
0
Unknown
22

12 reports had age data; 22 unknown.

Gender

Unknown/Not Reported
13
Female
19
Male
2

Reports by Year

Annual report counts from 2014–2024. Spike years may reflect recalls, media coverage, or litigation rather than changes in the product.

'14
'15
'16
'17
'18
'19
'20
'21
'22
'23
'24

Hover bars for exact counts.

← View all Plexus products in FDA data

Related Products

Plexus Slim (94) Plexus Bio Cleanse (45) Plexus Probio5 (38)

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