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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 BEVACIZUMAB-TNJN Cause Hepatic function abnormal? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Hepatic function abnormal have been filed in association with BEVACIZUMAB-TNJN (Avzivi tnjn). This represents 27.8% of all adverse event reports for BEVACIZUMAB-TNJN.

5
Reports of Hepatic function abnormal with BEVACIZUMAB-TNJN
27.8%
of all BEVACIZUMAB-TNJN reports
0
Deaths
5
Hospitalizations

How Dangerous Is Hepatic function abnormal From BEVACIZUMAB-TNJN?

Of the 5 reports, 5 (100.0%) required hospitalization, and 1 (20.0%) 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 BEVACIZUMAB-TNJN. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does BEVACIZUMAB-TNJN Cause?

Myelosuppression (6)

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)

Related Pages

BEVACIZUMAB-TNJN Full Profile All Hepatic function abnormal Reports All Drugs Causing Hepatic function abnormal BEVACIZUMAB-TNJN Demographics