Does ALENDRONATE Cause Product use in unapproved indication? 2,145 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,145 reports of Product use in unapproved indication have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 7.7% of all adverse event reports for ALENDRONATE.
2,145
Reports of Product use in unapproved indication with ALENDRONATE
7.7%
of all ALENDRONATE reports
1,110
Deaths
1,344
Hospitalizations
How Dangerous Is Product use in unapproved indication From ALENDRONATE?
Of the 2,145 reports, 1,110 (51.7%) resulted in death, 1,344 (62.7%) required hospitalization, and 1,336 (62.3%) were considered life-threatening.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 2,145 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 Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
Which ALENDRONATE Alternatives Have Lower Product use in unapproved indication Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID