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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does FOLIC ACID\VITAMINS Cause Product use issue? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Product use issue have been filed in association with FOLIC ACID\VITAMINS. This represents 20.0% of all adverse event reports for FOLIC ACID\VITAMINS.

9
Reports of Product use issue with FOLIC ACID\VITAMINS
20.0%
of all FOLIC ACID\VITAMINS reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product use issue From FOLIC ACID\VITAMINS?

Of the 9 reports.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for FOLIC ACID\VITAMINS. However, 9 reports have been filed with the FAERS database.

What Other Side Effects Does FOLIC ACID\VITAMINS Cause?

Maternal exposure timing unspecified (16) Maternal exposure during pregnancy (14) Gestational diabetes (10) Foetal exposure during pregnancy (9) Caesarean section (8) Atrial septal defect (7) Hyperemesis gravidarum (7) Normal newborn (7) Premature baby (6)

What Other Drugs Cause Product use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Related Pages

FOLIC ACID\VITAMINS Full Profile All Product use issue Reports All Drugs Causing Product use issue FOLIC ACID\VITAMINS Demographics