Does ALENDRONATE Cause Mobility decreased? 2,706 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,706 reports of Mobility decreased have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 9.7% of all adverse event reports for ALENDRONATE.
2,706
Reports of Mobility decreased with ALENDRONATE
9.7%
of all ALENDRONATE reports
1,633
Deaths
1,876
Hospitalizations
How Dangerous Is Mobility decreased From ALENDRONATE?
Of the 2,706 reports, 1,633 (60.3%) resulted in death, 1,876 (69.3%) required hospitalization, and 1,751 (64.7%) were considered life-threatening.
Is Mobility decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 2,706 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 Mobility decreased?
ADALIMUMAB (8,829)
ETANERCEPT (8,321)
METHOTREXATE (5,936)
ABATACEPT (4,519)
TOCILIZUMAB (4,403)
LEFLUNOMIDE (4,354)
HYDROXYCHLOROQUINE (4,105)
RITUXIMAB (4,067)
INFLIXIMAB (3,784)
TOFACITINIB (3,734)
Which ALENDRONATE Alternatives Have Lower Mobility decreased Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID