Does ALENDRONATE Cause Performance status decreased? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Performance status decreased have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 0.0% of all adverse event reports for ALENDRONATE.
6
Reports of Performance status decreased with ALENDRONATE
0.0%
of all ALENDRONATE reports
1
Deaths
5
Hospitalizations
How Dangerous Is Performance status decreased From ALENDRONATE?
Of the 6 reports, 1 (16.7%) resulted in death, 5 (83.3%) required hospitalization.
Is Performance status decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 6 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 Performance status decreased?
BACLOFEN (156)
LENALIDOMIDE (118)
PACLITAXEL (112)
BEVACIZUMAB (103)
SODIUM OXYBATE (103)
CARBOPLATIN (100)
DEXAMETHASONE (80)
CAPECITABINE (75)
NIRAPARIB (75)
LUMATEPERONE (68)
Which ALENDRONATE Alternatives Have Lower Performance status decreased Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID