Does ALENDRONATE\CHOLECALCIFEROL Cause Intentional product use issue? 344 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 344 reports of Intentional product use issue have been filed in association with ALENDRONATE\CHOLECALCIFEROL. This represents 13.2% of all adverse event reports for ALENDRONATE\CHOLECALCIFEROL.
344
Reports of Intentional product use issue with ALENDRONATE\CHOLECALCIFEROL
13.2%
of all ALENDRONATE\CHOLECALCIFEROL reports
269
Deaths
321
Hospitalizations
How Dangerous Is Intentional product use issue From ALENDRONATE\CHOLECALCIFEROL?
Of the 344 reports, 269 (78.2%) resulted in death, 321 (93.3%) required hospitalization, and 328 (95.3%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE\CHOLECALCIFEROL. However, 344 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which ALENDRONATE\CHOLECALCIFEROL Alternatives Have Lower Intentional product use issue Risk?
ALENDRONATE\CHOLECALCIFEROL vs ALENDRONIC ACID
ALENDRONATE\CHOLECALCIFEROL vs ALEVE
ALENDRONATE\CHOLECALCIFEROL vs ALEVE CAPLET
ALENDRONATE\CHOLECALCIFEROL vs ALEVE LIQUID
ALENDRONATE\CHOLECALCIFEROL vs ALFACALCIDOL