Does ALENDRONATE\CHOLECALCIFEROL Cause Incorrect product administration duration? 50 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 50 reports of Incorrect product administration duration have been filed in association with ALENDRONATE\CHOLECALCIFEROL. This represents 1.9% of all adverse event reports for ALENDRONATE\CHOLECALCIFEROL.
50
Reports of Incorrect product administration duration with ALENDRONATE\CHOLECALCIFEROL
1.9%
of all ALENDRONATE\CHOLECALCIFEROL reports
23
Deaths
23
Hospitalizations
How Dangerous Is Incorrect product administration duration From ALENDRONATE\CHOLECALCIFEROL?
Of the 50 reports, 23 (46.0%) resulted in death, 23 (46.0%) required hospitalization, and 23 (46.0%) 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 ALENDRONATE\CHOLECALCIFEROL. However, 50 reports have been filed with the FAERS database.
What Other Side Effects Does ALENDRONATE\CHOLECALCIFEROL Cause?
Fatigue (929)
Arthralgia (841)
Hypertension (820)
Depression (747)
Arthropathy (733)
Rash (726)
Alopecia (711)
Abdominal discomfort (705)
Confusional state (696)
Joint swelling (684)
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 ALENDRONATE\CHOLECALCIFEROL Alternatives Have Lower Incorrect product administration duration Risk?
ALENDRONATE\CHOLECALCIFEROL vs ALENDRONIC ACID
ALENDRONATE\CHOLECALCIFEROL vs ALEVE
ALENDRONATE\CHOLECALCIFEROL vs ALEVE CAPLET
ALENDRONATE\CHOLECALCIFEROL vs ALEVE LIQUID
ALENDRONATE\CHOLECALCIFEROL vs ALFACALCIDOL