Does ALENDRONATE Cause Device failure? 238 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 238 reports of Device failure have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 0.9% of all adverse event reports for ALENDRONATE.
238
Reports of Device failure with ALENDRONATE
0.9%
of all ALENDRONATE reports
9
Deaths
219
Hospitalizations
How Dangerous Is Device failure From ALENDRONATE?
Of the 238 reports, 9 (3.8%) resulted in death, 219 (92.0%) required hospitalization, and 5 (2.1%) were considered life-threatening.
Is Device failure Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 238 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 failure?
EPINEPHRINE (1,344)
SOMATROPIN (1,141)
PEGFILGRASTIM (829)
TREPROSTINIL (713)
BACLOFEN (691)
BUDESONIDE\FORMOTEROL (686)
ETANERCEPT (576)
GOLIMUMAB (487)
LEVONORGESTREL (332)
ACLIDINIUM (304)
Which ALENDRONATE Alternatives Have Lower Device failure Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID