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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 Febrile neutropenia? 39 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 39 reports of Febrile neutropenia have been filed in association with LURBINECTEDIN (ZEPZELCA). This represents 4.0% of all adverse event reports for LURBINECTEDIN.

39
Reports of Febrile neutropenia with LURBINECTEDIN
4.0%
of all LURBINECTEDIN reports
9
Deaths
29
Hospitalizations

How Dangerous Is Febrile neutropenia From LURBINECTEDIN?

Of the 39 reports, 9 (23.1%) resulted in death, 29 (74.4%) required hospitalization, and 5 (12.8%) were considered life-threatening.

Is Febrile neutropenia Listed in the Official Label?

Yes, Febrile neutropenia 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) Vomiting (37) Asthenia (36) Anaemia (34)

What Other Drugs Cause Febrile neutropenia?

CYCLOPHOSPHAMIDE (11,318) DOXORUBICIN (8,844) VINCRISTINE (8,676) RITUXIMAB (6,382) CYTARABINE (6,142) METHOTREXATE (6,091) ETOPOSIDE (5,966) CARBOPLATIN (4,888) DEXAMETHASONE (4,382) PREDNISONE (3,956)

Which LURBINECTEDIN Alternatives Have Lower Febrile neutropenia 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 Febrile neutropenia Reports All Drugs Causing Febrile neutropenia LURBINECTEDIN Demographics