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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 Platelet count decreased? 25 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 25 reports of Platelet count decreased have been filed in association with LURBINECTEDIN (ZEPZELCA). This represents 2.6% of all adverse event reports for LURBINECTEDIN.

25
Reports of Platelet count decreased with LURBINECTEDIN
2.6%
of all LURBINECTEDIN reports
5
Deaths
18
Hospitalizations

How Dangerous Is Platelet count decreased From LURBINECTEDIN?

Of the 25 reports, 5 (20.0%) resulted in death, 18 (72.0%) required hospitalization, and 3 (12.0%) were considered life-threatening.

Is Platelet count decreased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LURBINECTEDIN. However, 25 reports have been filed with the FAERS database.

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 Platelet count decreased?

LENALIDOMIDE (7,491) NIRAPARIB (4,102) ELTROMBOPAG OLAMINE (3,419) RUXOLITINIB (3,028) RITUXIMAB (2,404) VENETOCLAX (2,367) DEXAMETHASONE (2,321) PALBOCICLIB (2,277) CYCLOPHOSPHAMIDE (1,894) RIBAVIRIN (1,701)

Which LURBINECTEDIN Alternatives Have Lower Platelet count decreased 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 Platelet count decreased Reports All Drugs Causing Platelet count decreased LURBINECTEDIN Demographics