Does ALENDRONATE Cause Dislocation of vertebra? 767 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 767 reports of Dislocation of vertebra have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 2.8% of all adverse event reports for ALENDRONATE.
767
Reports of Dislocation of vertebra with ALENDRONATE
2.8%
of all ALENDRONATE reports
621
Deaths
659
Hospitalizations
How Dangerous Is Dislocation of vertebra From ALENDRONATE?
Of the 767 reports, 621 (81.0%) resulted in death, 659 (85.9%) required hospitalization, and 642 (83.7%) were considered life-threatening.
Is Dislocation of vertebra Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 767 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 Dislocation of vertebra?
ADALIMUMAB (942)
METHOTREXATE (900)
ABATACEPT (859)
DICLOFENAC (838)
RITUXIMAB (832)
TOCILIZUMAB (825)
LEFLUNOMIDE (810)
HYDROXYCHLOROQUINE (792)
FOLIC ACID (768)
SULFASALAZINE (756)
Which ALENDRONATE Alternatives Have Lower Dislocation of vertebra Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID