Does ALENDRONATE Cause Ulcer haemorrhage? 260 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 260 reports of Ulcer haemorrhage have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 0.9% of all adverse event reports for ALENDRONATE.
260
Reports of Ulcer haemorrhage with ALENDRONATE
0.9%
of all ALENDRONATE reports
96
Deaths
136
Hospitalizations
How Dangerous Is Ulcer haemorrhage From ALENDRONATE?
Of the 260 reports, 96 (36.9%) resulted in death, 136 (52.3%) required hospitalization, and 252 (96.9%) were considered life-threatening.
Is Ulcer haemorrhage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 260 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 Ulcer haemorrhage?
ADALIMUMAB (528)
ASPIRIN (439)
CLOPIDOGREL BISULFATE (419)
NAPROXEN (403)
PLAVIX (400)
METHOTREXATE (396)
RITUXIMAB (315)
DICLOFENAC (301)
TOCILIZUMAB (301)
TOFACITINIB (288)
Which ALENDRONATE Alternatives Have Lower Ulcer haemorrhage Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID