Does ALENDRONATE Cause Hyperlipidaemia? 511 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 511 reports of Hyperlipidaemia have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 1.8% of all adverse event reports for ALENDRONATE.
511
Reports of Hyperlipidaemia with ALENDRONATE
1.8%
of all ALENDRONATE reports
22
Deaths
497
Hospitalizations
How Dangerous Is Hyperlipidaemia From ALENDRONATE?
Of the 511 reports, 22 (4.3%) resulted in death, 497 (97.3%) required hospitalization, and 3 (0.6%) were considered life-threatening.
Is Hyperlipidaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 511 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 Hyperlipidaemia?
AMLODIPINE (226)
DENOSUMAB (204)
SITAGLIPTIN (186)
METHOTREXATE (184)
ROSUVASTATIN (179)
PREDNISONE (169)
FINASTERIDE (145)
MYCOPHENOLATE MOFETIL (141)
ASPIRIN (138)
METOPROLOL (138)
Which ALENDRONATE Alternatives Have Lower Hyperlipidaemia Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID