Does ALENDRONATE Cause Intentional product use issue? 2,422 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,422 reports of Intentional product use issue have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 8.7% of all adverse event reports for ALENDRONATE.
2,422
Reports of Intentional product use issue with ALENDRONATE
8.7%
of all ALENDRONATE reports
1,179
Deaths
1,409
Hospitalizations
How Dangerous Is Intentional product use issue From ALENDRONATE?
Of the 2,422 reports, 1,179 (48.7%) resulted in death, 1,409 (58.2%) required hospitalization, and 1,364 (56.3%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 2,422 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which ALENDRONATE Alternatives Have Lower Intentional product use issue Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID