🇺🇸 Probiotic dietary supplement in United States

14 US adverse-event reports

Safety signals — FAERS

Adverse reaction reports describe suspected side effects. A report does not mean the drug caused the event — co-medications, underlying disease and coincidence all contribute.

• Window: 22 April 2025 – 22 April 2026
• Total reports: 14

Most-reported reactions

1. Diarrhoea — 3 reports (21.43%)
2. Gait Disturbance — 2 reports (14.29%)
3. Insomnia — 2 reports (14.29%)
4. Abdominal Pain — 1 report (7.14%)
5. Abdominal Pain Upper — 1 report (7.14%)
6. Abnormal Behaviour — 1 report (7.14%)
7. Anal Haemorrhage — 1 report (7.14%)
8. Anal Incontinence — 1 report (7.14%)
9. Anxiety — 1 report (7.14%)
10. Arterial Stent Insertion — 1 report (7.14%)

Source database →

Frequently asked questions

Is Probiotic dietary supplement approved in United States?

Probiotic dietary supplement does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for Probiotic dietary supplement in United States?

University of New Mexico is the originator. The local marketing authorisation holder may differ — check the official source linked above.