Does ALENDRONATE Cause Product use issue? 4,398 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 4,398 reports of Product use issue have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 15.8% of all adverse event reports for ALENDRONATE.
4,398
Reports of Product use issue with ALENDRONATE
15.8%
of all ALENDRONATE reports
876
Deaths
1,581
Hospitalizations
How Dangerous Is Product use issue From ALENDRONATE?
Of the 4,398 reports, 876 (19.9%) resulted in death, 1,581 (35.9%) required hospitalization, and 1,215 (27.6%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 4,398 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 issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which ALENDRONATE Alternatives Have Lower Product use issue Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID