Does ALENDRONATE Cause Oesophageal ulcer? 38 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 38 reports of Oesophageal ulcer have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 0.1% of all adverse event reports for ALENDRONATE.
38
Reports of Oesophageal ulcer with ALENDRONATE
0.1%
of all ALENDRONATE reports
2
Deaths
22
Hospitalizations
How Dangerous Is Oesophageal ulcer From ALENDRONATE?
Of the 38 reports, 2 (5.3%) resulted in death, 22 (57.9%) required hospitalization, and 5 (13.2%) were considered life-threatening.
Is Oesophageal ulcer Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 38 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 Oesophageal ulcer?
TACROLIMUS (128)
DOXYCYCLINE (125)
ADALIMUMAB (119)
METHOTREXATE (104)
ASPIRIN (94)
PREDNISONE (94)
MYCOPHENOLATE MOFETIL (79)
IBUPROFEN (68)
PREDNISOLONE (59)
CLINDAMYCIN (54)
Which ALENDRONATE Alternatives Have Lower Oesophageal ulcer Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID