Does ALENDRONIC ACID Cause Off label use? 2,145 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,145 reports of Off label use have been filed in association with ALENDRONIC ACID. This represents 26.7% of all adverse event reports for ALENDRONIC ACID.
2,145
Reports of Off label use with ALENDRONIC ACID
26.7%
of all ALENDRONIC ACID reports
1,270
Deaths
1,476
Hospitalizations
How Dangerous Is Off label use From ALENDRONIC ACID?
Of the 2,145 reports, 1,270 (59.2%) resulted in death, 1,476 (68.8%) required hospitalization, and 1,523 (71.0%) were considered life-threatening.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALENDRONIC ACID. However, 2,145 reports have been filed with the FAERS database.
What Other Side Effects Does ALENDRONIC ACID Cause?
Fatigue (2,540)
Rheumatoid arthritis (2,352)
Pain (2,322)
Glossodynia (2,262)
Alopecia (2,227)
Systemic lupus erythematosus (2,225)
Rash (2,221)
Abdominal discomfort (2,208)
Hand deformity (2,150)
Arthralgia (2,117)
What Other Drugs Cause Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)
Which ALENDRONIC ACID Alternatives Have Lower Off label use Risk?
ALENDRONIC ACID vs ALEVE
ALENDRONIC ACID vs ALEVE CAPLET
ALENDRONIC ACID vs ALEVE LIQUID
ALENDRONIC ACID vs ALFACALCIDOL
ALENDRONIC ACID vs ALFENTANIL