Does PRALATREXATE Cause Hepatic function abnormal? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Hepatic function abnormal have been filed in association with PRALATREXATE (Pralatrexate). This represents 1.7% of all adverse event reports for PRALATREXATE.
8
Reports of Hepatic function abnormal with PRALATREXATE
1.7%
of all PRALATREXATE reports
3
Deaths
3
Hospitalizations
How Dangerous Is Hepatic function abnormal From PRALATREXATE?
Of the 8 reports, 3 (37.5%) resulted in death, 3 (37.5%) required hospitalization, and 5 (62.5%) 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 PRALATREXATE. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does PRALATREXATE Cause?
Malignant neoplasm progression (107)
Stomatitis (93)
Platelet count decreased (56)
Disease progression (46)
Neutrophil count decreased (40)
Anaemia (39)
Pyrexia (38)
Mucosal inflammation (37)
Drug ineffective (32)
Off label use (30)
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 PRALATREXATE Alternatives Have Lower Hepatic function abnormal Risk?
PRALATREXATE vs PRALSETINIB
PRALATREXATE vs PRAMIPEXOLE
PRALATREXATE vs PRAMIPEXOLE\PRAMIPEXOLE
PRALATREXATE vs PRAMLINTIDE
PRALATREXATE vs PRASTERONE