Does ERGOCALCIFEROL\RETINOL Cause Condition aggravated? 18 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Condition aggravated have been filed in association with ERGOCALCIFEROL\RETINOL. This represents 43.9% of all adverse event reports for ERGOCALCIFEROL\RETINOL.
18
Reports of Condition aggravated with ERGOCALCIFEROL\RETINOL
43.9%
of all ERGOCALCIFEROL\RETINOL reports
14
Deaths
18
Hospitalizations
How Dangerous Is Condition aggravated From ERGOCALCIFEROL\RETINOL?
Of the 18 reports, 14 (77.8%) resulted in death, 18 (100.0%) required hospitalization, and 14 (77.8%) 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 ERGOCALCIFEROL\RETINOL. However, 18 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 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)