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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 Sepsis? 19 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Sepsis have been filed in association with LURBINECTEDIN (ZEPZELCA). This represents 2.0% of all adverse event reports for LURBINECTEDIN.

19
Reports of Sepsis with LURBINECTEDIN
2.0%
of all LURBINECTEDIN reports
11
Deaths
14
Hospitalizations

How Dangerous Is Sepsis From LURBINECTEDIN?

Of the 19 reports, 11 (57.9%) resulted in death, 14 (73.7%) required hospitalization, and 4 (21.1%) were considered life-threatening.

Is Sepsis Listed in the Official Label?

Yes, Sepsis is listed as a known adverse reaction in the official FDA drug label for LURBINECTEDIN.

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 Sepsis?

RITUXIMAB (4,043) CYCLOPHOSPHAMIDE (4,041) METHOTREXATE (3,933) ADALIMUMAB (3,169) DEXAMETHASONE (3,150) LENALIDOMIDE (2,956) VINCRISTINE (2,791) DOXORUBICIN (2,740) PREDNISONE (2,634) PREDNISOLONE (2,281)

Which LURBINECTEDIN Alternatives Have Lower Sepsis 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 Sepsis Reports All Drugs Causing Sepsis LURBINECTEDIN Demographics