Does ALENDRONATE Cause Therapeutic product effect decreased? 3,585 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 3,585 reports of Therapeutic product effect decreased have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 12.9% of all adverse event reports for ALENDRONATE.
3,585
Reports of Therapeutic product effect decreased with ALENDRONATE
12.9%
of all ALENDRONATE reports
983
Deaths
1,732
Hospitalizations
How Dangerous Is Therapeutic product effect decreased From ALENDRONATE?
Of the 3,585 reports, 983 (27.4%) resulted in death, 1,732 (48.3%) required hospitalization, and 1,230 (34.3%) were considered life-threatening.
Is Therapeutic product effect decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 3,585 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 product effect decreased?
ADALIMUMAB (11,058)
METHOTREXATE (8,952)
ETANERCEPT (8,819)
ABATACEPT (7,256)
TOCILIZUMAB (7,208)
LEFLUNOMIDE (7,025)
HYDROXYCHLOROQUINE (6,450)
INFLIXIMAB (6,401)
RITUXIMAB (6,281)
GOLIMUMAB (5,478)
Which ALENDRONATE Alternatives Have Lower Therapeutic product effect decreased Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID