Does ALENDRONATE\CHOLECALCIFEROL Cause Device failure? 49 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 49 reports of Device failure have been filed in association with ALENDRONATE\CHOLECALCIFEROL. This represents 1.9% of all adverse event reports for ALENDRONATE\CHOLECALCIFEROL.
49
Reports of Device failure with ALENDRONATE\CHOLECALCIFEROL
1.9%
of all ALENDRONATE\CHOLECALCIFEROL reports
0
Deaths
47
Hospitalizations
How Dangerous Is Device failure From ALENDRONATE\CHOLECALCIFEROL?
Of the 49 reports, 47 (95.9%) required hospitalization.
Is Device failure Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE\CHOLECALCIFEROL. However, 49 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 Device failure?
EPINEPHRINE (1,344)
SOMATROPIN (1,141)
PEGFILGRASTIM (829)
TREPROSTINIL (713)
BACLOFEN (691)
BUDESONIDE\FORMOTEROL (686)
ETANERCEPT (576)
GOLIMUMAB (487)
LEVONORGESTREL (332)
ACLIDINIUM (304)
Which ALENDRONATE\CHOLECALCIFEROL Alternatives Have Lower Device failure Risk?
ALENDRONATE\CHOLECALCIFEROL vs ALENDRONIC ACID
ALENDRONATE\CHOLECALCIFEROL vs ALEVE
ALENDRONATE\CHOLECALCIFEROL vs ALEVE CAPLET
ALENDRONATE\CHOLECALCIFEROL vs ALEVE LIQUID
ALENDRONATE\CHOLECALCIFEROL vs ALFACALCIDOL