Does VITAMIN A Cause Intentional product use issue? 60 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 60 reports of Intentional product use issue have been filed in association with VITAMIN A (SKINEEZ). This represents 8.8% of all adverse event reports for VITAMIN A.
60
Reports of Intentional product use issue with VITAMIN A
8.8%
of all VITAMIN A reports
58
Deaths
60
Hospitalizations
How Dangerous Is Intentional product use issue From VITAMIN A?
Of the 60 reports, 58 (96.7%) resulted in death, 60 (100.0%) required hospitalization, and 55 (91.7%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VITAMIN A. However, 60 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which VITAMIN A Alternatives Have Lower Intentional product use issue Risk?
VITAMIN A vs VITAMIN B
VITAMIN A vs VITAMIN D NOS
VITAMIN A vs VITAMINS
VITAMIN A vs VOCLOSPORIN
VITAMIN A vs VOGLIBOSE