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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 Thrombocytopenia? 48 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 48 reports of Thrombocytopenia have been filed in association with LURBINECTEDIN (ZEPZELCA). This represents 5.0% of all adverse event reports for LURBINECTEDIN.

48
Reports of Thrombocytopenia with LURBINECTEDIN
5.0%
of all LURBINECTEDIN reports
9
Deaths
22
Hospitalizations

How Dangerous Is Thrombocytopenia From LURBINECTEDIN?

Of the 48 reports, 9 (18.8%) resulted in death, 22 (45.8%) required hospitalization, and 3 (6.3%) were considered life-threatening.

Is Thrombocytopenia Listed in the Official Label?

Yes, Thrombocytopenia 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) Fatigue (43) Febrile neutropenia (39) Vomiting (37) Asthenia (36) Anaemia (34)

What Other Drugs Cause Thrombocytopenia?

DEXAMETHASONE (5,873) RITUXIMAB (4,810) CYCLOPHOSPHAMIDE (4,669) LENALIDOMIDE (4,584) CARBOPLATIN (4,483) METHOTREXATE (3,865) DOXORUBICIN (3,638) ETOPOSIDE (3,085) VINCRISTINE (2,940) OXALIPLATIN (2,886)

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