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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 VITAMIN A Cause Adverse event? 24 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 24 reports of Adverse event have been filed in association with VITAMIN A (SKINEEZ). This represents 3.5% of all adverse event reports for VITAMIN A.

24
Reports of Adverse event with VITAMIN A
3.5%
of all VITAMIN A reports
24
Deaths
24
Hospitalizations

How Dangerous Is Adverse event From VITAMIN A?

Of the 24 reports, 24 (100.0%) resulted in death, 24 (100.0%) required hospitalization, and 22 (91.7%) were considered life-threatening.

Is Adverse event Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for VITAMIN A. However, 24 reports have been filed with the FAERS database.

What Other Side Effects Does VITAMIN A Cause?

Off label use (243) Gastrooesophageal reflux disease (202) Drug ineffective (181) Product use in unapproved indication (168) Swelling (166) Nausea (161) Somnolence (156) Drug hypersensitivity (144) Pain (143) Dyspnoea (140)

What Other Drugs Cause Adverse event?

ABATACEPT (4,028) APIXABAN (3,871) ETANERCEPT (3,096) LENALIDOMIDE (2,426) INFLIXIMAB (2,269) ADALIMUMAB (2,121) METHOTREXATE (1,846) LEFLUNOMIDE (1,476) RIVAROXABAN (1,465) ALENDRONATE (1,462)

Which VITAMIN A Alternatives Have Lower Adverse event Risk?

VITAMIN A vs VITAMIN B VITAMIN A vs VITAMIN D NOS VITAMIN A vs VITAMINS VITAMIN A vs VOCLOSPORIN VITAMIN A vs VOGLIBOSE

Related Pages

VITAMIN A Full Profile All Adverse event Reports All Drugs Causing Adverse event VITAMIN A Demographics