Does ALENDRONATE Cause Intentional product misuse? 102 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 102 reports of Intentional product misuse have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 0.4% of all adverse event reports for ALENDRONATE.
102
Reports of Intentional product misuse with ALENDRONATE
0.4%
of all ALENDRONATE reports
65
Deaths
83
Hospitalizations
How Dangerous Is Intentional product misuse From ALENDRONATE?
Of the 102 reports, 65 (63.7%) resulted in death, 83 (81.4%) required hospitalization, and 80 (78.4%) were considered life-threatening.
Is Intentional product misuse 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which ALENDRONATE Alternatives Have Lower Intentional product misuse Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID