Does ALENDRONATE Cause Onychomadesis? 627 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 627 reports of Onychomadesis have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 2.3% of all adverse event reports for ALENDRONATE.
627
Reports of Onychomadesis with ALENDRONATE
2.3%
of all ALENDRONATE reports
515
Deaths
562
Hospitalizations
How Dangerous Is Onychomadesis From ALENDRONATE?
Of the 627 reports, 515 (82.1%) resulted in death, 562 (89.6%) required hospitalization, and 453 (72.2%) were considered life-threatening.
Is Onychomadesis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 627 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 Onychomadesis?
ADALIMUMAB (797)
METHOTREXATE (785)
RITUXIMAB (722)
TOCILIZUMAB (721)
ABATACEPT (703)
INFLIXIMAB (682)
SECUKINUMAB (678)
LEFLUNOMIDE (667)
GOLIMUMAB (660)
HYDROXYCHLOROQUINE (660)
Which ALENDRONATE Alternatives Have Lower Onychomadesis Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID