Does ERGOCALCIFEROL\RETINOL Cause Product use issue? 28 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Product use issue have been filed in association with ERGOCALCIFEROL\RETINOL. This represents 68.3% of all adverse event reports for ERGOCALCIFEROL\RETINOL.
28
Reports of Product use issue with ERGOCALCIFEROL\RETINOL
68.3%
of all ERGOCALCIFEROL\RETINOL reports
28
Deaths
28
Hospitalizations
How Dangerous Is Product use issue From ERGOCALCIFEROL\RETINOL?
Of the 28 reports, 28 (100.0%) resulted in death, 28 (100.0%) required hospitalization, and 28 (100.0%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ERGOCALCIFEROL\RETINOL. However, 28 reports have been filed with the FAERS database.
What Other Side Effects Does ERGOCALCIFEROL\RETINOL Cause?
Off label use (35)
Rash (34)
Nausea (33)
Onychomadesis (33)
Pemphigus (33)
Pericarditis (33)
Psoriatic arthropathy (33)
Rheumatoid arthritis (33)
Swelling (33)
Synovitis (33)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)