Does ALENDRONATE Cause Incorrect product administration duration? 287 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 287 reports of Incorrect product administration duration have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 1.0% of all adverse event reports for ALENDRONATE.
287
Reports of Incorrect product administration duration with ALENDRONATE
1.0%
of all ALENDRONATE reports
67
Deaths
72
Hospitalizations
How Dangerous Is Incorrect product administration duration From ALENDRONATE?
Of the 287 reports, 67 (23.3%) resulted in death, 72 (25.1%) required hospitalization, and 64 (22.3%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 287 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which ALENDRONATE Alternatives Have Lower Incorrect product administration duration Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID