Does ALENDRONATE Cause Ill-defined disorder? 2,392 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,392 reports of Ill-defined disorder have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 8.6% of all adverse event reports for ALENDRONATE.
2,392
Reports of Ill-defined disorder with ALENDRONATE
8.6%
of all ALENDRONATE reports
1,189
Deaths
1,677
Hospitalizations
How Dangerous Is Ill-defined disorder From ALENDRONATE?
Of the 2,392 reports, 1,189 (49.7%) resulted in death, 1,677 (70.1%) required hospitalization, and 1,343 (56.1%) were considered life-threatening.
Is Ill-defined disorder Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 2,392 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 Ill-defined disorder?
ACETAMINOPHEN\OXYCODONE (9,780)
ACETAMINOPHEN\HYDROCODONE (6,159)
TOCILIZUMAB (4,411)
RITUXIMAB (4,220)
ETANERCEPT (4,202)
METHOTREXATE (4,063)
ABATACEPT (3,630)
LUTETIUM LU-177 VIPIVOTIDE TETRAXETAN (3,600)
LEFLUNOMIDE (3,570)
CERTOLIZUMAB PEGOL (3,273)
Which ALENDRONATE Alternatives Have Lower Ill-defined disorder Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID