Does ALENDRONATE Cause Barrett's oesophagus? 53 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 53 reports of Barrett's oesophagus have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 0.2% of all adverse event reports for ALENDRONATE.
53
Reports of Barrett's oesophagus with ALENDRONATE
0.2%
of all ALENDRONATE reports
6
Deaths
41
Hospitalizations
How Dangerous Is Barrett's oesophagus From ALENDRONATE?
Of the 53 reports, 6 (11.3%) resulted in death, 41 (77.4%) required hospitalization, and 4 (7.5%) were considered life-threatening.
Is Barrett's oesophagus Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 53 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 Barrett's oesophagus?
ESOMEPRAZOLE (272)
RANITIDINE (232)
OMEPRAZOLE (148)
OLMESARTAN MEDOXOMIL (105)
ADALIMUMAB (80)
HYDROCHLOROTHIAZIDE\OLMESARTAN MEDOXOMIL (69)
LANSOPRAZOLE (55)
PANTOPRAZOLE (49)
SODIUM OXYBATE (49)
ETORICOXIB (44)
Which ALENDRONATE Alternatives Have Lower Barrett's oesophagus Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID