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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does CRIZOTINIB Cause Hepatic function abnormal? 123 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 123 reports of Hepatic function abnormal have been filed in association with CRIZOTINIB (Xalkori). This represents 1.2% of all adverse event reports for CRIZOTINIB.

123
Reports of Hepatic function abnormal with CRIZOTINIB
1.2%
of all CRIZOTINIB reports
7
Deaths
53
Hospitalizations

How Dangerous Is Hepatic function abnormal From CRIZOTINIB?

Of the 123 reports, 7 (5.7%) resulted in death, 53 (43.1%) required hospitalization, and 5 (4.1%) 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 CRIZOTINIB. However, 123 reports have been filed with the FAERS database.

What Other Side Effects Does CRIZOTINIB Cause?

Death (2,028) Neoplasm progression (1,161) Nausea (820) Disease progression (677) Diarrhoea (631) Vomiting (600) Fatigue (419) Off label use (353) Dyspnoea (352) Visual impairment (315)

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 CRIZOTINIB Alternatives Have Lower Hepatic function abnormal Risk?

CRIZOTINIB vs CROFELEMER CRIZOTINIB vs CROMOLYN CRIZOTINIB vs CROTALIDAE POLYVALENT IMMUNE FAB CRIZOTINIB vs CUBICIN CRIZOTINIB vs CUPRIC

Related Pages

CRIZOTINIB Full Profile All Hepatic function abnormal Reports All Drugs Causing Hepatic function abnormal CRIZOTINIB Demographics