Does ALENDRONATE Cause Device breakage? 102 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 102 reports of Device breakage have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 0.4% of all adverse event reports for ALENDRONATE.
102
Reports of Device breakage with ALENDRONATE
0.4%
of all ALENDRONATE reports
3
Deaths
96
Hospitalizations
How Dangerous Is Device breakage From ALENDRONATE?
Of the 102 reports, 3 (2.9%) resulted in death, 96 (94.1%) required hospitalization, and 1 (1.0%) were considered life-threatening.
Is Device breakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 102 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 Device breakage?
COPPER (9,201)
SOMATROPIN (7,761)
ETONOGESTREL (4,140)
LEVONORGESTREL (2,726)
ETHINYL ESTRADIOL\ETONOGESTREL (741)
CARBIDOPA\LEVODOPA (634)
TREPROSTINIL (396)
ADALIMUMAB (375)
ALBUTEROL (256)
EPOPROSTENOL (240)
Which ALENDRONATE Alternatives Have Lower Device breakage Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID