Does RETINOL Cause Intentional product use issue? 28 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Intentional product use issue have been filed in association with RETINOL (HYDRASPHERE PLUS). This represents 9.5% of all adverse event reports for RETINOL.
28
Reports of Intentional product use issue with RETINOL
9.5%
of all RETINOL reports
28
Deaths
28
Hospitalizations
How Dangerous Is Intentional product use issue From RETINOL?
Of the 28 reports, 28 (100.0%) resulted in death, 28 (100.0%) required hospitalization, and 22 (78.6%) 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 RETINOL. However, 28 reports have been filed with the FAERS database.
What Other Side Effects Does RETINOL Cause?
Gastrooesophageal reflux disease (113)
Somnolence (86)
Coma (85)
Pneumonia aspiration (85)
Off label use (82)
Drug ineffective (64)
Infusion related reaction (49)
Type 2 diabetes mellitus (49)
Confusional state (45)
Pain (44)
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 RETINOL Alternatives Have Lower Intentional product use issue Risk?
RETINOL vs REVATIO
RETINOL vs REVEFENACIN
RETINOL vs REVLIMID
RETINOL vs REVOLADE
RETINOL vs REVUMENIB