Does ERGOCALCIFEROL Cause Onychomadesis? 347 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 347 reports of Onychomadesis have been filed in association with ERGOCALCIFEROL (Ergocalciferol Capsules,). This represents 6.3% of all adverse event reports for ERGOCALCIFEROL.
347
Reports of Onychomadesis with ERGOCALCIFEROL
6.3%
of all ERGOCALCIFEROL reports
347
Deaths
285
Hospitalizations
How Dangerous Is Onychomadesis From ERGOCALCIFEROL?
Of the 347 reports, 347 (100.0%) resulted in death, 285 (82.1%) required hospitalization, and 287 (82.7%) were considered life-threatening.
Is Onychomadesis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ERGOCALCIFEROL. However, 347 reports have been filed with the FAERS database.
What Other Side Effects Does ERGOCALCIFEROL Cause?
Dyspnoea (1,485)
Asthma (1,453)
Wheezing (1,394)
Drug ineffective (1,300)
Pain (1,245)
Pneumonia (1,176)
Vomiting (1,071)
Therapeutic product effect incomplete (1,068)
Drug hypersensitivity (1,065)
Nausea (993)
What Other Drugs Cause Onychomadesis?
ADALIMUMAB (797)
METHOTREXATE (785)
RITUXIMAB (722)
TOCILIZUMAB (721)
ABATACEPT (703)
INFLIXIMAB (682)
SECUKINUMAB (678)
LEFLUNOMIDE (667)
GOLIMUMAB (660)
HYDROXYCHLOROQUINE (660)
Which ERGOCALCIFEROL Alternatives Have Lower Onychomadesis Risk?
ERGOCALCIFEROL vs ERGOCALCIFEROL\PHYTONADIONE\RETINOL\TOCOPHEROL
ERGOCALCIFEROL vs ERIBULIN
ERGOCALCIFEROL vs ERLOTINIB
ERGOCALCIFEROL vs ERTAPENEM
ERGOCALCIFEROL vs ERTUGLIFLOZIN PIDOLATE