Does GEMCITABINE Cause Hepatic function abnormal? 162 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 162 reports of Hepatic function abnormal have been filed in association with GEMCITABINE (Gemcitabine). This represents 0.5% of all adverse event reports for GEMCITABINE.
162
Reports of Hepatic function abnormal with GEMCITABINE
0.5%
of all GEMCITABINE reports
17
Deaths
61
Hospitalizations
How Dangerous Is Hepatic function abnormal From GEMCITABINE?
Of the 162 reports, 17 (10.5%) resulted in death, 61 (37.7%) required hospitalization, and 15 (9.3%) were considered life-threatening.
Is Hepatic function abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GEMCITABINE. However, 162 reports have been filed with the FAERS database.
What Other Side Effects Does GEMCITABINE Cause?
Off label use (3,319)
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)
What Other Drugs Cause Hepatic function abnormal?
NIVOLUMAB (1,131)
PEMBROLIZUMAB (1,079)
METHOTREXATE (1,054)
CABOZANTINIB S-MALATE (912)
CYCLOPHOSPHAMIDE (824)
BEVACIZUMAB (769)
PACLITAXEL (603)
LENVATINIB (528)
ATORVASTATIN (520)
CYCLOSPORINE (508)
Which GEMCITABINE Alternatives Have Lower Hepatic function abnormal Risk?
GEMCITABINE vs GEMCITABINE\GEMCITABINE
GEMCITABINE vs GEMFIBROZIL
GEMCITABINE vs GEMTUZUMAB OZOGAMICIN
GEMCITABINE vs GEMZAR
GEMCITABINE vs GENTAMICIN