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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 TRABECTEDIN Cause Hepatic function abnormal? 39 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 39 reports of Hepatic function abnormal have been filed in association with TRABECTEDIN (YONDELIS). This represents 2.0% of all adverse event reports for TRABECTEDIN.

39
Reports of Hepatic function abnormal with TRABECTEDIN
2.0%
of all TRABECTEDIN reports
7
Deaths
23
Hospitalizations

How Dangerous Is Hepatic function abnormal From TRABECTEDIN?

Of the 39 reports, 7 (17.9%) resulted in death, 23 (59.0%) required hospitalization, and 5 (12.8%) 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 TRABECTEDIN. However, 39 reports have been filed with the FAERS database.

What Other Side Effects Does TRABECTEDIN Cause?

Neutropenia (207) Anaemia (189) Thrombocytopenia (172) Nausea (160) Febrile neutropenia (142) Pancytopenia (124) Vomiting (121) Rhabdomyolysis (117) Off label use (105) Alanine aminotransferase increased (104)

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 TRABECTEDIN Alternatives Have Lower Hepatic function abnormal Risk?

TRABECTEDIN vs TRACLEER TRABECTEDIN vs TRADJENTA TRABECTEDIN vs TRALOKINUMAB-LDRM TRABECTEDIN vs TRAMADOL TRABECTEDIN vs TRAMADOL\TRAMADOL

Related Pages

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