Does ALENDRONATE Cause Intramedullary rod insertion? 1,192 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,192 reports of Intramedullary rod insertion have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 4.3% of all adverse event reports for ALENDRONATE.
1,192
Reports of Intramedullary rod insertion with ALENDRONATE
4.3%
of all ALENDRONATE reports
39
Deaths
1,166
Hospitalizations
How Dangerous Is Intramedullary rod insertion From ALENDRONATE?
Of the 1,192 reports, 39 (3.3%) resulted in death, 1,166 (97.8%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Intramedullary rod insertion Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 1,192 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 Intramedullary rod insertion?
FOSAMAX (372)
ALENDRONATE\CHOLECALCIFEROL (221)
IBANDRONATE (111)
FOSAMAX PLUS D (90)
RISEDRONATE (45)
BONIVA (31)
ACTONEL (25)
ZOLEDRONIC ACID (16)
DENOSUMAB (9)
ALENDRONIC ACID (8)
Which ALENDRONATE Alternatives Have Lower Intramedullary rod insertion Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID