Does ALENDRONATE Cause Condition aggravated? 4,125 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 4,125 reports of Condition aggravated have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 14.8% of all adverse event reports for ALENDRONATE.
4,125
Reports of Condition aggravated with ALENDRONATE
14.8%
of all ALENDRONATE reports
1,531
Deaths
2,272
Hospitalizations
How Dangerous Is Condition aggravated From ALENDRONATE?
Of the 4,125 reports, 1,531 (37.1%) resulted in death, 2,272 (55.1%) required hospitalization, and 1,948 (47.2%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 4,125 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which ALENDRONATE Alternatives Have Lower Condition aggravated Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID