Does ALENDRONATE Cause Contraindicated product administered? 5,940 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5,940 reports of Contraindicated product administered have been filed in association with ALENDRONATE (ALENDRONATE SODIUM). This represents 21.3% of all adverse event reports for ALENDRONATE.
5,940
Reports of Contraindicated product administered with ALENDRONATE
21.3%
of all ALENDRONATE reports
1,156
Deaths
2,040
Hospitalizations
How Dangerous Is Contraindicated product administered From ALENDRONATE?
Of the 5,940 reports, 1,156 (19.5%) resulted in death, 2,040 (34.3%) required hospitalization, and 1,501 (25.3%) were considered life-threatening.
Is Contraindicated product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONATE. However, 5,940 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 Contraindicated product administered?
ABATACEPT (13,559)
METHOTREXATE (13,121)
ETANERCEPT (12,062)
TOCILIZUMAB (11,547)
ADALIMUMAB (11,270)
LEFLUNOMIDE (11,206)
HYDROXYCHLOROQUINE (10,557)
RITUXIMAB (10,479)
INFLIXIMAB (9,618)
SULFASALAZINE (8,698)
Which ALENDRONATE Alternatives Have Lower Contraindicated product administered Risk?
ALENDRONATE vs ALENDRONATE\CHOLECALCIFEROL
ALENDRONATE vs ALENDRONIC ACID
ALENDRONATE vs ALEVE
ALENDRONATE vs ALEVE CAPLET
ALENDRONATE vs ALEVE LIQUID