🇺🇸 Folic acid, vit B12 in United States

5 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: 5

Most-reported reactions

1. Confusional State — 1 report (20%)
2. Fatigue — 1 report (20%)
3. Full Blood Count Abnormal — 1 report (20%)
4. Lower Gastrointestinal Haemorrhage — 1 report (20%)
5. Upper Respiratory Tract Infection — 1 report (20%)

Source database →

Frequently asked questions

Is Folic acid, vit B12 approved in United States?

Folic acid, vit B12 does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for Folic acid, vit B12 in United States?

AGUNCO Obstetrics and Gynecology Centre is the originator. The local marketing authorisation holder may differ — check the official source linked above.