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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 Myelosuppression? 13 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Myelosuppression have been filed in association with LURBINECTEDIN (ZEPZELCA). This represents 1.4% of all adverse event reports for LURBINECTEDIN.

13
Reports of Myelosuppression with LURBINECTEDIN
1.4%
of all LURBINECTEDIN reports
0
Deaths
3
Hospitalizations

How Dangerous Is Myelosuppression From LURBINECTEDIN?

Of the 13 reports, 3 (23.1%) required hospitalization.

Is Myelosuppression Listed in the Official Label?

Yes, Myelosuppression 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 Myelosuppression?

CYCLOPHOSPHAMIDE (3,603) CARBOPLATIN (2,624) TRASTUZUMAB (2,552) PACLITAXEL (2,522) TISLELIZUMAB (2,142) CYTARABINE (1,869) VENETOCLAX (1,864) CISPLATIN (1,849) BEVACIZUMAB (1,744) SODIUM (1,696)

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