Does ALENDRONATE Cause Full blood count abnormal? 270 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 270 reports of Full blood count abnormal have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 1.0% of all adverse event reports for ALENDRONATE.
270
Reports of Full blood count abnormal with ALENDRONATE
1.0%
of all ALENDRONATE reports
55
Deaths
200
Hospitalizations
How Dangerous Is Full blood count abnormal From ALENDRONATE?
Of the 270 reports, 55 (20.4%) resulted in death, 200 (74.1%) required hospitalization, and 169 (62.6%) were considered life-threatening.
Is Full blood count abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 270 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 Full blood count abnormal?
ALBUTEROL (3,060)
PREDNISONE (2,230)
BUDESONIDE\FORMOTEROL (1,786)
TIOTROPIUM (1,754)
MONTELUKAST (1,529)
MEPOLIZUMAB (1,440)
BUDESONIDE (1,339)
PALBOCICLIB (1,146)
CICLESONIDE (916)
PANTOPRAZOLE (776)
Which ALENDRONATE Alternatives Have Lower Full blood count abnormal Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID