Does ALENDRONATE Cause Adverse event? 1,462 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,462 reports of Adverse event have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 5.2% of all adverse event reports for ALENDRONATE.
1,462
Reports of Adverse event with ALENDRONATE
5.2%
of all ALENDRONATE reports
452
Deaths
929
Hospitalizations
How Dangerous Is Adverse event From ALENDRONATE?
Of the 1,462 reports, 452 (30.9%) resulted in death, 929 (63.5%) required hospitalization, and 560 (38.3%) were considered life-threatening.
Is Adverse event Listed in the Official Label?
Yes, Adverse event is listed as a known adverse reaction in the official FDA drug label for ALENDRONATE.
What Other Side Effects Does ALENDRONATE Cause?
Pain (8,989)
Abdominal discomfort (8,301)
Alopecia (8,286)
Systemic lupus erythematosus (8,139)
Fatigue (8,011)
Rheumatoid arthritis (8,010)
Pemphigus (7,947)
Drug ineffective (7,880)
Glossodynia (7,289)
Swelling (6,458)
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)
RISPERIDONE (1,440)
Which ALENDRONATE Alternatives Have Lower Adverse event Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID