Does ALENDRONATE Cause Hypersensitivity? 5,233 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5,233 reports of Hypersensitivity have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 18.8% of all adverse event reports for ALENDRONATE.
5,233
Reports of Hypersensitivity with ALENDRONATE
18.8%
of all ALENDRONATE reports
1,568
Deaths
2,502
Hospitalizations
How Dangerous Is Hypersensitivity From ALENDRONATE?
Of the 5,233 reports, 1,568 (30.0%) resulted in death, 2,502 (47.8%) required hospitalization, and 1,926 (36.8%) were considered life-threatening.
Is Hypersensitivity Listed in the Official Label?
Yes, Hypersensitivity is listed as a known adverse reaction in the official FDA drug label for ALENDRONATE.
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 Hypersensitivity?
ETANERCEPT (10,846)
ADALIMUMAB (10,641)
METHOTREXATE (9,799)
TOCILIZUMAB (9,076)
ABATACEPT (8,945)
INFLIXIMAB (8,519)
RITUXIMAB (8,408)
ADAPALENE (8,356)
LEFLUNOMIDE (7,926)
CERTOLIZUMAB PEGOL (7,353)
Which ALENDRONATE Alternatives Have Lower Hypersensitivity Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID