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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 LURBINECTEDIN Cause Hepatic enzyme increased? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Hepatic enzyme increased have been filed in association with LURBINECTEDIN (ZEPZELCA). This represents 0.6% of all adverse event reports for LURBINECTEDIN.

6
Reports of Hepatic enzyme increased with LURBINECTEDIN
0.6%
of all LURBINECTEDIN reports
2
Deaths
2
Hospitalizations

How Dangerous Is Hepatic enzyme increased From LURBINECTEDIN?

Of the 6 reports, 2 (33.3%) resulted in death, 2 (33.3%) required hospitalization, and 1 (16.7%) were considered life-threatening.

Is Hepatic enzyme increased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LURBINECTEDIN. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does LURBINECTEDIN Cause?

Death (129) Disease progression (98) Off label use (69) Neutropenia (59) Nausea (58) Thrombocytopenia (48) Fatigue (43) Febrile neutropenia (39) Vomiting (37) Asthenia (36)

What Other Drugs Cause Hepatic enzyme increased?

METHOTREXATE (9,857) ADALIMUMAB (8,693) TOCILIZUMAB (7,691) ETANERCEPT (7,481) ABATACEPT (7,397) RITUXIMAB (7,247) LEFLUNOMIDE (7,173) INFLIXIMAB (6,778) HYDROXYCHLOROQUINE (6,555) TOFACITINIB (6,269)

Which LURBINECTEDIN Alternatives Have Lower Hepatic enzyme increased Risk?

LURBINECTEDIN vs LUSPATERCEPT LURBINECTEDIN vs LUSPATERCEPT-AAMT LURBINECTEDIN vs LUTEIN LURBINECTEDIN vs LUTETIUM LU-177 LURBINECTEDIN vs LUTETIUM LU-177 VIPIVOTIDE TETRAXETAN

Related Pages

LURBINECTEDIN Full Profile All Hepatic enzyme increased Reports All Drugs Causing Hepatic enzyme increased LURBINECTEDIN Demographics