Does ALENDRONATE Cause Haematemesis? 172 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 172 reports of Haematemesis have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 0.6% of all adverse event reports for ALENDRONATE.
172
Reports of Haematemesis with ALENDRONATE
0.6%
of all ALENDRONATE reports
100
Deaths
65
Hospitalizations
How Dangerous Is Haematemesis From ALENDRONATE?
Of the 172 reports, 100 (58.1%) resulted in death, 65 (37.8%) required hospitalization, and 9 (5.2%) were considered life-threatening.
Is Haematemesis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 172 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 Haematemesis?
ASPIRIN (1,538)
RIVAROXABAN (1,085)
CLOPIDOGREL BISULFATE (954)
IBUPROFEN (836)
APIXABAN (650)
ADALIMUMAB (563)
ACETAMINOPHEN (454)
WARFARIN (426)
SERTRALINE (412)
ENOXAPARIN (404)
Which ALENDRONATE Alternatives Have Lower Haematemesis Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID