Does ALENDRONATE Cause Eosinophil count increased? 136 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 136 reports of Eosinophil count increased have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 0.5% of all adverse event reports for ALENDRONATE.
136
Reports of Eosinophil count increased with ALENDRONATE
0.5%
of all ALENDRONATE reports
1
Deaths
134
Hospitalizations
How Dangerous Is Eosinophil count increased From ALENDRONATE?
Of the 136 reports, 1 (0.7%) resulted in death, 134 (98.5%) required hospitalization.
Is Eosinophil count increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 136 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 Eosinophil count increased?
ALBUTEROL (1,359)
PREDNISONE (846)
BUDESONIDE\FORMOTEROL (719)
DUPILUMAB (712)
TIOTROPIUM (682)
MEPOLIZUMAB (670)
MONTELUKAST (504)
BUDESONIDE (493)
CLOZAPINE (475)
FLUTICASONE\SALMETEROL (416)
Which ALENDRONATE Alternatives Have Lower Eosinophil count increased Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID