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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 Hypersensitivity? 59 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 59 reports of Hypersensitivity have been filed in association with VITAMIN A (SKINEEZ). This represents 8.7% of all adverse event reports for VITAMIN A.

59
Reports of Hypersensitivity with VITAMIN A
8.7%
of all VITAMIN A reports
38
Deaths
39
Hospitalizations

How Dangerous Is Hypersensitivity From VITAMIN A?

Of the 59 reports, 38 (64.4%) resulted in death, 39 (66.1%) required hospitalization, and 38 (64.4%) were considered life-threatening.

Is Hypersensitivity Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for VITAMIN A. However, 59 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 Hypersensitivity?

ETANERCEPT (10,846) ADALIMUMAB (10,641) METHOTREXATE (9,799) TOCILIZUMAB (9,076) ABATACEPT (8,945) INFLIXIMAB (8,519) RITUXIMAB (8,408) ADAPALENE (8,356) LEFLUNOMIDE (7,926) CERTOLIZUMAB PEGOL (7,353)

Which VITAMIN A Alternatives Have Lower Hypersensitivity 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 Hypersensitivity Reports All Drugs Causing Hypersensitivity VITAMIN A Demographics