Does ALENDRONATE Cause Unevaluable event? 47 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 47 reports of Unevaluable event have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 0.2% of all adverse event reports for ALENDRONATE.
47
Reports of Unevaluable event with ALENDRONATE
0.2%
of all ALENDRONATE reports
1
Deaths
29
Hospitalizations
How Dangerous Is Unevaluable event From ALENDRONATE?
Of the 47 reports, 1 (2.1%) resulted in death, 29 (61.7%) required hospitalization, and 8 (17.0%) were considered life-threatening.
Is Unevaluable event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 47 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 Unevaluable event?
ADALIMUMAB (4,242)
ETANERCEPT (3,902)
LENALIDOMIDE (3,331)
OXYCODONE (3,145)
AMBRISENTAN (2,336)
SODIUM OXYBATE (2,328)
CARBIDOPA\LEVODOPA (1,632)
DUPILUMAB (1,410)
MORPHINE (1,161)
ACETAMINOPHEN\HYDROCODONE (1,118)
Which ALENDRONATE Alternatives Have Lower Unevaluable event Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID