Does CHOLECALCIFEROL Cause Incorrect product administration duration? 78 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 78 reports of Incorrect product administration duration have been filed in association with CHOLECALCIFEROL (Floriva). This represents 0.7% of all adverse event reports for CHOLECALCIFEROL.
78
Reports of Incorrect product administration duration with CHOLECALCIFEROL
0.7%
of all CHOLECALCIFEROL reports
63
Deaths
68
Hospitalizations
How Dangerous Is Incorrect product administration duration From CHOLECALCIFEROL?
Of the 78 reports, 63 (80.8%) resulted in death, 68 (87.2%) required hospitalization, and 62 (79.5%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CHOLECALCIFEROL. However, 78 reports have been filed with the FAERS database.
What Other Side Effects Does CHOLECALCIFEROL Cause?
Drug ineffective (2,792)
Off label use (2,642)
Fatigue (2,303)
Pain (2,230)
Vomiting (1,898)
Dyspnoea (1,837)
Headache (1,822)
Arthralgia (1,768)
Rash (1,674)
Nausea (1,672)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which CHOLECALCIFEROL Alternatives Have Lower Incorrect product administration duration Risk?
CHOLECALCIFEROL vs CHOLECALCIFEROL\ERGOCALCIFEROL
CHOLECALCIFEROL vs CHOLESTYRAMINE
CHOLECALCIFEROL vs CHOLIC ACID
CHOLECALCIFEROL vs CHONDROITIN
CHOLECALCIFEROL vs CHONDROITIN \GLUCOSAMINE