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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 DURVALUMAB Cause Hepatic function abnormal? 210 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 210 reports of Hepatic function abnormal have been filed in association with DURVALUMAB (IMFINZI). This represents 1.2% of all adverse event reports for DURVALUMAB.

210
Reports of Hepatic function abnormal with DURVALUMAB
1.2%
of all DURVALUMAB reports
28
Deaths
99
Hospitalizations

How Dangerous Is Hepatic function abnormal From DURVALUMAB?

Of the 210 reports, 28 (13.3%) resulted in death, 99 (47.1%) required hospitalization, and 25 (11.9%) 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 DURVALUMAB. However, 210 reports have been filed with the FAERS database.

What Other Side Effects Does DURVALUMAB Cause?

Death (2,817) Malignant neoplasm progression (1,330) Pneumonitis (827) Radiation pneumonitis (786) Pyrexia (573) Diarrhoea (530) Pneumonia (453) Dyspnoea (444) Interstitial lung disease (430) Off label use (395)

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 DURVALUMAB Alternatives Have Lower Hepatic function abnormal Risk?

DURVALUMAB vs DUTASTERIDE DURVALUMAB vs DUTASTERIDE\TAMSULOSIN DURVALUMAB vs DUVELISIB DURVALUMAB vs DYDROGESTERONE DURVALUMAB vs EBASTINE

Related Pages

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