Does ALENDRONATE Cause Off label use? 4,579 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 4,579 reports of Off label use have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 16.4% of all adverse event reports for ALENDRONATE.
4,579
Reports of Off label use with ALENDRONATE
16.4%
of all ALENDRONATE reports
1,718
Deaths
2,605
Hospitalizations
How Dangerous Is Off label use From ALENDRONATE?
Of the 4,579 reports, 1,718 (37.5%) resulted in death, 2,605 (56.9%) required hospitalization, and 2,214 (48.4%) were considered life-threatening.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 4,579 reports have been filed with the FAERS database.
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 Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)
Which ALENDRONATE Alternatives Have Lower Off label use Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID