Does ERGOCALCIFEROL Cause Recalled product? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Recalled product have been filed in association with ERGOCALCIFEROL (Ergocalciferol Capsules,). This represents 0.1% of all adverse event reports for ERGOCALCIFEROL.
5
Reports of Recalled product with ERGOCALCIFEROL
0.1%
of all ERGOCALCIFEROL reports
0
Deaths
4
Hospitalizations
How Dangerous Is Recalled product From ERGOCALCIFEROL?
Of the 5 reports, 4 (80.0%) required hospitalization, and 1 (20.0%) were considered life-threatening.
Is Recalled product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ERGOCALCIFEROL. However, 5 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 Recalled product?
PARATHYROID HORMONE (900)
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (80)
CALCITRIOL (68)
CALCIUM (66)
REMDESIVIR (36)
LEVOTHYROXINE\LIOTHYRONINE (34)
TESTOSTERONE (32)
VALSARTAN (32)
CHLORHEXIDINE (28)
ALCOHOL (26)
Which ERGOCALCIFEROL Alternatives Have Lower Recalled product Risk?
ERGOCALCIFEROL vs ERGOCALCIFEROL\PHYTONADIONE\RETINOL\TOCOPHEROL
ERGOCALCIFEROL vs ERIBULIN
ERGOCALCIFEROL vs ERLOTINIB
ERGOCALCIFEROL vs ERTAPENEM
ERGOCALCIFEROL vs ERTUGLIFLOZIN PIDOLATE