prenatal vitamin
Prenatal Vitamin (Prenatal Multivitamin) is a dietary supplement.
Prenatal Multivitamin
Key facts
- Active ingredient
- Prenatal Multivitamin
- Type
- Supplement
What is Prenatal Vitamin?
From the FDA label:Multivitamin formulated for pregnancy with folate, iron, and DHA.
What the evidence says
What Prenatal Vitamin 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.
Ways to save
Ask for the generic
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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.
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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 Prenatal Multivitamin
The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 212 reports naming Prenatal Multivitamin — the active ingredient in Prenatal Vitamin, and the FDA flagged 58% 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:
- maternal exposure during pregnancy25 reports
- fatigue14 reports
- diarrhoea12 reports
- exposure during pregnancy12 reports
- nausea10 reports
- vomiting9 reports
- pain in extremity8 reports
- arthralgia7 reports
Read these as a signal, not a rate. A report does not mean Prenatal Multivitamin 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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