Does ALENDRONATE Cause Hypercholesterolaemia? 1,607 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,607 reports of Hypercholesterolaemia have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 5.8% of all adverse event reports for ALENDRONATE.
1,607
Reports of Hypercholesterolaemia with ALENDRONATE
5.8%
of all ALENDRONATE reports
1,226
Deaths
1,271
Hospitalizations
How Dangerous Is Hypercholesterolaemia From ALENDRONATE?
Of the 1,607 reports, 1,226 (76.3%) resulted in death, 1,271 (79.1%) required hospitalization, and 958 (59.6%) were considered life-threatening.
Is Hypercholesterolaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 1,607 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 Hypercholesterolaemia?
METHOTREXATE (1,547)
TOCILIZUMAB (1,483)
ADALIMUMAB (1,479)
ABATACEPT (1,410)
RITUXIMAB (1,389)
PREDNISONE (1,377)
INFLIXIMAB (1,338)
DICLOFENAC (1,331)
LEFLUNOMIDE (1,322)
CERTOLIZUMAB PEGOL (1,321)
Which ALENDRONATE Alternatives Have Lower Hypercholesterolaemia Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID