Does POLATUZUMAB VEDOTIN Cause Hepatic function abnormal? 41 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 41 reports of Hepatic function abnormal have been filed in association with POLATUZUMAB VEDOTIN (POLIVY). This represents 0.9% of all adverse event reports for POLATUZUMAB VEDOTIN.
41
Reports of Hepatic function abnormal with POLATUZUMAB VEDOTIN
0.9%
of all POLATUZUMAB VEDOTIN reports
5
Deaths
13
Hospitalizations
How Dangerous Is Hepatic function abnormal From POLATUZUMAB VEDOTIN?
Of the 41 reports, 5 (12.2%) resulted in death, 13 (31.7%) required hospitalization, and 3 (7.3%) 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 POLATUZUMAB VEDOTIN. However, 41 reports have been filed with the FAERS database.
What Other Side Effects Does POLATUZUMAB VEDOTIN Cause?
Disease progression (1,131)
Off label use (692)
Anaemia (344)
Blood lactate dehydrogenase increased (307)
Drug ineffective (305)
Neutropenia (303)
Death (295)
Covid-19 (286)
Febrile neutropenia (286)
Pyrexia (285)
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 POLATUZUMAB VEDOTIN Alternatives Have Lower Hepatic function abnormal Risk?
POLATUZUMAB VEDOTIN vs POLATUZUMAB VEDOTIN-PIIQ
POLATUZUMAB VEDOTIN vs POLIDOCANOL
POLATUZUMAB VEDOTIN vs POLYETHYLENE GLYCOL
POLATUZUMAB VEDOTIN vs POLYETHYLENE GLYCOL 3350
POLATUZUMAB VEDOTIN vs POLYETHYLENE GLYCOL 3350\POTASSIUM\SODIUM BICARBONATE\SODIUM