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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 Dehydration? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Dehydration have been filed in association with LURBINECTEDIN (ZEPZELCA). This represents 0.7% of all adverse event reports for LURBINECTEDIN.

7
Reports of Dehydration with LURBINECTEDIN
0.7%
of all LURBINECTEDIN reports
0
Deaths
7
Hospitalizations

How Dangerous Is Dehydration From LURBINECTEDIN?

Of the 7 reports, 7 (100.0%) required hospitalization, and 1 (14.3%) were considered life-threatening.

Is Dehydration Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LURBINECTEDIN. However, 7 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 Dehydration?

LENALIDOMIDE (3,469) ADALIMUMAB (3,233) CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (3,168) FUROSEMIDE (2,195) SEMAGLUTIDE (1,816) METFORMIN (1,754) CAPECITABINE (1,599) LENVATINIB (1,526) TIRZEPATIDE (1,187) SACUBITRIL\VALSARTAN (1,171)

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