Does ALENDRONATE Cause Therapy non-responder? 975 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 975 reports of Therapy non-responder have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 3.5% of all adverse event reports for ALENDRONATE.
975
Reports of Therapy non-responder with ALENDRONATE
3.5%
of all ALENDRONATE reports
444
Deaths
802
Hospitalizations
How Dangerous Is Therapy non-responder From ALENDRONATE?
Of the 975 reports, 444 (45.5%) resulted in death, 802 (82.3%) required hospitalization, and 625 (64.1%) were considered life-threatening.
Is Therapy non-responder Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 975 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 Therapy non-responder?
ETANERCEPT (3,472)
APREMILAST (3,360)
METHOTREXATE (2,965)
RITUXIMAB (2,731)
ADALIMUMAB (2,595)
PREDNISONE (2,563)
TREPROSTINIL (2,289)
INFLIXIMAB (2,122)
TOCILIZUMAB (1,775)
HYDROXYCHLOROQUINE (1,699)
Which ALENDRONATE Alternatives Have Lower Therapy non-responder Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID