Does ERGOCALCIFEROL Cause Intentional product use issue? 410 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 410 reports of Intentional product use issue have been filed in association with ERGOCALCIFEROL (Ergocalciferol Capsules,). This represents 7.5% of all adverse event reports for ERGOCALCIFEROL.
410
Reports of Intentional product use issue with ERGOCALCIFEROL
7.5%
of all ERGOCALCIFEROL reports
360
Deaths
297
Hospitalizations
How Dangerous Is Intentional product use issue From ERGOCALCIFEROL?
Of the 410 reports, 360 (87.8%) resulted in death, 297 (72.4%) required hospitalization, and 276 (67.3%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ERGOCALCIFEROL. However, 410 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which ERGOCALCIFEROL Alternatives Have Lower Intentional product use issue Risk?
ERGOCALCIFEROL vs ERGOCALCIFEROL\PHYTONADIONE\RETINOL\TOCOPHEROL
ERGOCALCIFEROL vs ERIBULIN
ERGOCALCIFEROL vs ERLOTINIB
ERGOCALCIFEROL vs ERTAPENEM
ERGOCALCIFEROL vs ERTUGLIFLOZIN PIDOLATE