vitamin b6
Vitamin B6 (Pyridoxine) is a dietary supplement.
Pyridoxine
Key facts
- Active ingredient
- Pyridoxine
- Drug class
- Vitamin B6 Analog
- Type
- Supplement
What the evidence says
What Vitamin B6 is
Commonly used for
What the evidence shows
Typical dosage
Safety
Side effects
Interactions & cautions
Sources
This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease. Summarized from public health authorities; general reference, not medical advice. Talk to a licensed healthcare professional before starting any supplement.
Drug class
Ways to save
Ask for the generic
Same active ingredient, far cheaper. Is there a generic? →
Request a 90-day supply
Bulk fills usually lower the per-dose price vs monthly refills.
Use copay cards
Manufacturer copay cards & patient-assistance programs — especially for brand drugs.
Compare alternatives
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Frequently asked questions
- What class of drug is Vitamin B6?
- Vitamin B6 is classified as vitamin b6 analog, per the FDA's Established Pharmacologic Class.
Information is sourced from public FDA regulatory data. Provided for general reference only — not medical advice. Always consult a licensed professional and the current prescribing information.
What people report to the FDA about Pyridoxine
The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 17,204 reports naming Pyridoxine — the active ingredient in Vitamin B6, and the FDA flagged 85% of those reports as serious. The effects reported most often — leaving out reports about overdose, misuse or the condition being treated, which dominate the raw list for common medicines:
- nausea1,453 reports
- fatigue1,151 reports
- vomiting1,132 reports
- diarrhoea1,080 reports
- headache1,016 reports
- dyspnoea897 reports
- anaemia887 reports
- pyrexia883 reports
Read these as a signal, not a rate. A report does not mean Pyridoxine caused the effect — anyone can file one, and many describe people taking several medicines for several conditions. Crucially there is no denominator: FAERS does not record how many people took the drug, so these counts cannot be turned into “X% of patients” — a bigger number often just means a more widely used or more talked-about drug. Duplicates exist, and publicity drives reporting. For what is actually established, read the FDA label.
Source: openFDA drug/event (FAERS), retrieved September 26, 2026.
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