Does VITAMIN A Cause Condition aggravated? 112 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 112 reports of Condition aggravated have been filed in association with VITAMIN A (SKINEEZ). This represents 16.5% of all adverse event reports for VITAMIN A.
112
Reports of Condition aggravated with VITAMIN A
16.5%
of all VITAMIN A reports
107
Deaths
102
Hospitalizations
How Dangerous Is Condition aggravated From VITAMIN A?
Of the 112 reports, 107 (95.5%) resulted in death, 102 (91.1%) required hospitalization, and 104 (92.9%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VITAMIN A. However, 112 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which VITAMIN A Alternatives Have Lower Condition aggravated Risk?
VITAMIN A vs VITAMIN B
VITAMIN A vs VITAMIN D NOS
VITAMIN A vs VITAMINS
VITAMIN A vs VOCLOSPORIN
VITAMIN A vs VOGLIBOSE