Does GEMCITABINE Cause Off label use? 3,319 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 3,319 reports of Off label use have been filed in association with GEMCITABINE (Gemcitabine). This represents 10.6% of all adverse event reports for GEMCITABINE.
3,319
Reports of Off label use with GEMCITABINE
10.6%
of all GEMCITABINE reports
496
Deaths
1,162
Hospitalizations
How Dangerous Is Off label use From GEMCITABINE?
Of the 3,319 reports, 496 (14.9%) resulted in death, 1,162 (35.0%) required hospitalization, and 364 (11.0%) 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 GEMCITABINE. However, 3,319 reports have been filed with the FAERS database.
What Other Side Effects Does GEMCITABINE Cause?
Disease progression (3,123)
Thrombocytopenia (2,320)
Drug ineffective (2,003)
Malignant neoplasm progression (1,962)
Neutropenia (1,892)
Anaemia (1,745)
Pyrexia (1,511)
Nausea (1,336)
Myelosuppression (1,197)
Fatigue (1,098)
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 GEMCITABINE Alternatives Have Lower Off label use Risk?
GEMCITABINE vs GEMCITABINE\GEMCITABINE
GEMCITABINE vs GEMFIBROZIL
GEMCITABINE vs GEMTUZUMAB OZOGAMICIN
GEMCITABINE vs GEMZAR
GEMCITABINE vs GENTAMICIN