The most commonly reported side effects of vitamin a palmitate include nausea, fatigue, and dyspnoea, based on 5,065 FDA adverse event reports from 2004 to 2025. 4.7% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for vitamin a palmitate.
These are voluntary reports and do not establish that vitamin a palmitate caused these reactions.
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Other drugs that appear in adverse event reports alongside vitamin a palmitate. Drugs flagged as a suspected cause appear in the first column. Drugs taken at the same time but not suspected appear in the second.
Also suspected
Taken alongside
Co-occurrence in adverse event reports does not establish a drug interaction. Patients often take multiple medications, and these lists reflect prescribing patterns rather than causal relationships. Consult a healthcare provider about potential drug interactions.
63.4% of vitamin a palmitate adverse event reports involve female patients and 31.9% involve male patients. The largest age group is adult at 58%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking vitamin a palmitate when the adverse event was reported.
Showing 15 of 208 indications
Vitamin A Palmitate is sold under the brand name Vi-dom-a.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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