Greens Supplement

AG1 Whole Food Pouch 360G Non Specific

97 adverse event reports submitted to the FDA · 2024–2025 · 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 97 reports. One report may include multiple reactions — reaction totals may exceed the report count.

Aspartate aminotransferase increased
15
Diarrhoea
13
Alanine aminotransferase increased
13
Hepatic enzyme increased
11
Nausea
11
Vomiting
8
Hypersensitivity
7
Anaphylactic reaction
6
Abdominal pain upper
6
Dehydration
6

Reported Outcomes

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

OutcomeReports
Other Serious or Important Medical Event 90
Hospitalization 30
Visited Emergency Room 21
Allergic Reaction 11
Life Threatening 6
Visited a Health Care Provider 6
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
8
35–49
20
50–64
19
65–79
9
80+
0
Unknown
41

56 reports had age data; 41 unknown.

Gender

Female
53
Male
44
Unknown/Not Reported
0

Reports by Year

Annual report counts from 2024–2025. Spike years may reflect recalls, media coverage, or litigation rather than changes in the product.

'24
'25

Hover bars for exact counts.

Context about this data: Reports heavily concentrated in 2024 (69% of total). High concentration may reflect a recall, enforcement action, batch filing, or litigation-driven reporting rather than ongoing consumer use.

← View all AG1 products in FDA data

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