Does ERGOCALCIFEROL Cause Product use issue? 353 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 353 reports of Product use issue have been filed in association with ERGOCALCIFEROL (Ergocalciferol Capsules,). This represents 6.4% of all adverse event reports for ERGOCALCIFEROL.
353
Reports of Product use issue with ERGOCALCIFEROL
6.4%
of all ERGOCALCIFEROL reports
298
Deaths
265
Hospitalizations
How Dangerous Is Product use issue From ERGOCALCIFEROL?
Of the 353 reports, 298 (84.4%) resulted in death, 265 (75.1%) required hospitalization, and 266 (75.4%) 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. However, 353 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 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)
Which ERGOCALCIFEROL Alternatives Have Lower Product use issue Risk?
ERGOCALCIFEROL vs ERGOCALCIFEROL\PHYTONADIONE\RETINOL\TOCOPHEROL
ERGOCALCIFEROL vs ERIBULIN
ERGOCALCIFEROL vs ERLOTINIB
ERGOCALCIFEROL vs ERTAPENEM
ERGOCALCIFEROL vs ERTUGLIFLOZIN PIDOLATE