🇺🇸 Daily Vitamin D3 in United States

11 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: 11

Most-reported reactions

1. Anxiety — 2 reports (18.18%)
2. Abdominal Discomfort — 1 report (9.09%)
3. Alopecia — 1 report (9.09%)
4. Arthralgia — 1 report (9.09%)
5. Chest Discomfort — 1 report (9.09%)
6. Chest Pain — 1 report (9.09%)
7. Condition Aggravated — 1 report (9.09%)
8. Depression — 1 report (9.09%)
9. Diarrhoea — 1 report (9.09%)
10. Discomfort — 1 report (9.09%)

Source database →

Frequently asked questions

Is Daily Vitamin D3 approved in United States?

Daily Vitamin D3 does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for Daily Vitamin D3 in United States?

Medical University of South Carolina is the originator. The local marketing authorisation holder may differ — check the official source linked above.