Does ALENDRONATE Cause Complication associated with device? 37 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 37 reports of Complication associated with device have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 0.1% of all adverse event reports for ALENDRONATE.
37
Reports of Complication associated with device with ALENDRONATE
0.1%
of all ALENDRONATE reports
2
Deaths
34
Hospitalizations
How Dangerous Is Complication associated with device From ALENDRONATE?
Of the 37 reports, 2 (5.4%) resulted in death, 34 (91.9%) required hospitalization.
Is Complication associated with device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 37 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 Complication associated with device?
ETONOGESTREL (6,047)
COPPER (1,083)
BACLOFEN (525)
TREPROSTINIL (422)
EPOPROSTENOL (399)
LEVONORGESTREL (344)
ADALIMUMAB (269)
CARBIDOPA\LEVODOPA (169)
MACITENTAN (169)
TEDUGLUTIDE (133)
Which ALENDRONATE Alternatives Have Lower Complication associated with device Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID