Does ALENDRONATE Cause Therapeutic response decreased? 513 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 513 reports of Therapeutic response decreased have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 1.8% of all adverse event reports for ALENDRONATE.
513
Reports of Therapeutic response decreased with ALENDRONATE
1.8%
of all ALENDRONATE reports
122
Deaths
398
Hospitalizations
How Dangerous Is Therapeutic response decreased From ALENDRONATE?
Of the 513 reports, 122 (23.8%) resulted in death, 398 (77.6%) required hospitalization, and 234 (45.6%) were considered life-threatening.
Is Therapeutic response decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 513 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 Therapeutic response decreased?
DUPILUMAB (7,824)
ETANERCEPT (3,460)
ONABOTULINUMTOXINA (2,685)
METHOTREXATE (2,668)
INFLIXIMAB (1,991)
RITUXIMAB (1,728)
LEFLUNOMIDE (1,574)
TOCILIZUMAB (1,512)
HYDROXYCHLOROQUINE (1,485)
ADALIMUMAB (1,357)
Which ALENDRONATE Alternatives Have Lower Therapeutic response decreased Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID