Does ALENDRONATE Cause Haemoglobin decreased? 283 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 283 reports of Haemoglobin decreased have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 1.0% of all adverse event reports for ALENDRONATE.
283
Reports of Haemoglobin decreased with ALENDRONATE
1.0%
of all ALENDRONATE reports
23
Deaths
239
Hospitalizations
How Dangerous Is Haemoglobin decreased From ALENDRONATE?
Of the 283 reports, 23 (8.1%) resulted in death, 239 (84.5%) required hospitalization, and 34 (12.0%) were considered life-threatening.
Is Haemoglobin decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 283 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 Haemoglobin decreased?
LENALIDOMIDE (4,031)
RUXOLITINIB (3,297)
ECULIZUMAB (3,028)
ADALIMUMAB (2,459)
CLOZAPINE (2,396)
RITUXIMAB (1,803)
APIXABAN (1,779)
NIRAPARIB (1,759)
METHOTREXATE (1,754)
RIBAVIRIN (1,753)
Which ALENDRONATE Alternatives Have Lower Haemoglobin decreased Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID