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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does ERGOCALCIFEROL\RETINOL Cause Ill-defined disorder? 21 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Ill-defined disorder have been filed in association with ERGOCALCIFEROL\RETINOL. This represents 51.2% of all adverse event reports for ERGOCALCIFEROL\RETINOL.

21
Reports of Ill-defined disorder with ERGOCALCIFEROL\RETINOL
51.2%
of all ERGOCALCIFEROL\RETINOL reports
21
Deaths
21
Hospitalizations

How Dangerous Is Ill-defined disorder From ERGOCALCIFEROL\RETINOL?

Of the 21 reports, 21 (100.0%) resulted in death, 21 (100.0%) required hospitalization, and 21 (100.0%) were considered life-threatening.

Is Ill-defined disorder Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ERGOCALCIFEROL\RETINOL. However, 21 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 Ill-defined disorder?

ACETAMINOPHEN\OXYCODONE (9,780) ACETAMINOPHEN\HYDROCODONE (6,159) TOCILIZUMAB (4,411) RITUXIMAB (4,220) ETANERCEPT (4,202) METHOTREXATE (4,063) ABATACEPT (3,630) LUTETIUM LU-177 VIPIVOTIDE TETRAXETAN (3,600) LEFLUNOMIDE (3,570) CERTOLIZUMAB PEGOL (3,273)

Related Pages

ERGOCALCIFEROL\RETINOL Full Profile All Ill-defined disorder Reports All Drugs Causing Ill-defined disorder ERGOCALCIFEROL\RETINOL Demographics