Does ALENDRONATE Cause Hyperkeratosis? 26 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 26 reports of Hyperkeratosis have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 0.1% of all adverse event reports for ALENDRONATE.
26
Reports of Hyperkeratosis with ALENDRONATE
0.1%
of all ALENDRONATE reports
0
Deaths
24
Hospitalizations
How Dangerous Is Hyperkeratosis From ALENDRONATE?
Of the 26 reports, 24 (92.3%) required hospitalization.
Is Hyperkeratosis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 26 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 Hyperkeratosis?
CABOZANTINIB S-MALATE (411)
ADALIMUMAB (332)
SUNITINIB MALATE (170)
ETANERCEPT (168)
SORAFENIB (150)
METHOTREXATE (149)
VEMURAFENIB (145)
REGORAFENIB (136)
RIPRETINIB (124)
RITUXIMAB (121)
Which ALENDRONATE Alternatives Have Lower Hyperkeratosis Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID