🇺🇸 Nutritional supplements in United States

83 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: 23 April 2025 – 23 April 2026
• Total reports: 83

Most-reported reactions

1. Dizziness — 12 reports (14.46%)
2. Dyspnoea — 11 reports (13.25%)
3. Paraesthesia — 9 reports (10.84%)
4. Asthenia — 8 reports (9.64%)
5. Fatigue — 8 reports (9.64%)
6. Pneumonia — 8 reports (9.64%)
7. Headache — 7 reports (8.43%)
8. Nausea — 7 reports (8.43%)
9. Pyrexia — 7 reports (8.43%)
10. Anaemia — 6 reports (7.23%)

Source database →

Frequently asked questions

Is Nutritional supplements approved in United States?

Nutritional supplements does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for Nutritional supplements in United States?

Johns Hopkins Bloomberg School of Public Health is the originator. The local marketing authorisation holder may differ — check the official source linked above.