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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 Contraindicated product administered? 95 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 95 reports of Contraindicated product administered have been filed in association with VITAMIN A (SKINEEZ). This represents 14.0% of all adverse event reports for VITAMIN A.

95
Reports of Contraindicated product administered with VITAMIN A
14.0%
of all VITAMIN A reports
94
Deaths
94
Hospitalizations

How Dangerous Is Contraindicated product administered From VITAMIN A?

Of the 95 reports, 94 (98.9%) resulted in death, 94 (98.9%) required hospitalization, and 94 (98.9%) were considered life-threatening.

Is Contraindicated product administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for VITAMIN A. However, 95 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 Contraindicated product administered?

ABATACEPT (13,559) METHOTREXATE (13,121) ETANERCEPT (12,062) TOCILIZUMAB (11,547) ADALIMUMAB (11,270) LEFLUNOMIDE (11,206) HYDROXYCHLOROQUINE (10,557) RITUXIMAB (10,479) INFLIXIMAB (9,618) SULFASALAZINE (8,698)

Which VITAMIN A Alternatives Have Lower Contraindicated product administered 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 Contraindicated product administered Reports All Drugs Causing Contraindicated product administered VITAMIN A Demographics