Does ALENDRONATE Cause Intentional dose omission? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Intentional dose omission have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 0.1% of all adverse event reports for ALENDRONATE.
16
Reports of Intentional dose omission with ALENDRONATE
0.1%
of all ALENDRONATE reports
4
Deaths
4
Hospitalizations
How Dangerous Is Intentional dose omission From ALENDRONATE?
Of the 16 reports, 4 (25.0%) resulted in death, 4 (25.0%) required hospitalization, and 3 (18.8%) were considered life-threatening.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 16 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 dose omission?
DUPILUMAB (2,269)
CERTOLIZUMAB PEGOL (1,253)
ADALIMUMAB (845)
TOFACITINIB (845)
INFLIXIMAB (815)
ABALOPARATIDE (623)
ETANERCEPT (615)
AMBRISENTAN (595)
SODIUM OXYBATE (580)
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)
Which ALENDRONATE Alternatives Have Lower Intentional dose omission Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID