Does CHOLECALCIFEROL Cause Recalled product? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Recalled product have been filed in association with CHOLECALCIFEROL (Floriva). This represents 0.1% of all adverse event reports for CHOLECALCIFEROL.
10
Reports of Recalled product with CHOLECALCIFEROL
0.1%
of all CHOLECALCIFEROL reports
1
Deaths
5
Hospitalizations
How Dangerous Is Recalled product From CHOLECALCIFEROL?
Of the 10 reports, 1 (10.0%) resulted in death, 5 (50.0%) required hospitalization, and 2 (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 CHOLECALCIFEROL. However, 10 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 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 CHOLECALCIFEROL Alternatives Have Lower Recalled product Risk?
CHOLECALCIFEROL vs CHOLECALCIFEROL\ERGOCALCIFEROL
CHOLECALCIFEROL vs CHOLESTYRAMINE
CHOLECALCIFEROL vs CHOLIC ACID
CHOLECALCIFEROL vs CHONDROITIN
CHOLECALCIFEROL vs CHONDROITIN \GLUCOSAMINE