🇺🇸 Vitamin B12, Vitamin B6, Folic acid in United States

4 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: 4

Most-reported reactions

1. Asthenia — 1 report (25%)
2. Nasopharyngitis — 1 report (25%)
3. Weight Increased — 1 report (25%)
4. Wound Haemorrhage — 1 report (25%)

Source database →

Frequently asked questions

Is Vitamin B12, Vitamin B6, Folic acid approved in United States?

Vitamin B12, Vitamin B6, Folic acid does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for Vitamin B12, Vitamin B6, Folic acid in United States?

Medice Arzneimittel Pütter GmbH & Co KG is the originator. The local marketing authorisation holder may differ — check the official source linked above.