Does ERGOCALCIFEROL Cause Product quality issue? 232 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 232 reports of Product quality issue have been filed in association with ERGOCALCIFEROL (Ergocalciferol Capsules,). This represents 4.2% of all adverse event reports for ERGOCALCIFEROL.
232
Reports of Product quality issue with ERGOCALCIFEROL
4.2%
of all ERGOCALCIFEROL reports
231
Deaths
157
Hospitalizations
How Dangerous Is Product quality issue From ERGOCALCIFEROL?
Of the 232 reports, 231 (99.6%) resulted in death, 157 (67.7%) required hospitalization, and 159 (68.5%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ERGOCALCIFEROL. However, 232 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which ERGOCALCIFEROL Alternatives Have Lower Product quality issue Risk?
ERGOCALCIFEROL vs ERGOCALCIFEROL\PHYTONADIONE\RETINOL\TOCOPHEROL
ERGOCALCIFEROL vs ERIBULIN
ERGOCALCIFEROL vs ERLOTINIB
ERGOCALCIFEROL vs ERTAPENEM
ERGOCALCIFEROL vs ERTUGLIFLOZIN PIDOLATE