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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 Hypersensitivity? 10 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Hypersensitivity have been filed in association with ERGOCALCIFEROL\RETINOL. This represents 24.4% of all adverse event reports for ERGOCALCIFEROL\RETINOL.

10
Reports of Hypersensitivity with ERGOCALCIFEROL\RETINOL
24.4%
of all ERGOCALCIFEROL\RETINOL reports
9
Deaths
9
Hospitalizations

How Dangerous Is Hypersensitivity From ERGOCALCIFEROL\RETINOL?

Of the 10 reports, 9 (90.0%) resulted in death, 9 (90.0%) required hospitalization, and 9 (90.0%) were considered life-threatening.

Is Hypersensitivity Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ERGOCALCIFEROL\RETINOL. However, 10 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 Hypersensitivity?

ETANERCEPT (10,846) ADALIMUMAB (10,641) METHOTREXATE (9,799) TOCILIZUMAB (9,076) ABATACEPT (8,945) INFLIXIMAB (8,519) RITUXIMAB (8,408) ADAPALENE (8,356) LEFLUNOMIDE (7,926) CERTOLIZUMAB PEGOL (7,353)

Related Pages

ERGOCALCIFEROL\RETINOL Full Profile All Hypersensitivity Reports All Drugs Causing Hypersensitivity ERGOCALCIFEROL\RETINOL Demographics