Does ALENDRONATE\CHOLECALCIFEROL Cause Adverse event? 202 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 202 reports of Adverse event have been filed in association with ALENDRONATE\CHOLECALCIFEROL. This represents 7.8% of all adverse event reports for ALENDRONATE\CHOLECALCIFEROL.
202
Reports of Adverse event with ALENDRONATE\CHOLECALCIFEROL
7.8%
of all ALENDRONATE\CHOLECALCIFEROL reports
81
Deaths
177
Hospitalizations
How Dangerous Is Adverse event From ALENDRONATE\CHOLECALCIFEROL?
Of the 202 reports, 81 (40.1%) resulted in death, 177 (87.6%) required hospitalization, and 120 (59.4%) were considered life-threatening.
Is Adverse event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE\CHOLECALCIFEROL. However, 202 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 Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which ALENDRONATE\CHOLECALCIFEROL Alternatives Have Lower Adverse event Risk?
ALENDRONATE\CHOLECALCIFEROL vs ALENDRONIC ACID
ALENDRONATE\CHOLECALCIFEROL vs ALEVE
ALENDRONATE\CHOLECALCIFEROL vs ALEVE CAPLET
ALENDRONATE\CHOLECALCIFEROL vs ALEVE LIQUID
ALENDRONATE\CHOLECALCIFEROL vs ALFACALCIDOL