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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 BREXUCABTAGENE AUTOLEUCEL Cause Nausea? 30 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 30 reports of Nausea have been filed in association with BREXUCABTAGENE AUTOLEUCEL (TECARTUS). This represents 1.7% of all adverse event reports for BREXUCABTAGENE AUTOLEUCEL.

30
Reports of Nausea with BREXUCABTAGENE AUTOLEUCEL
1.7%
of all BREXUCABTAGENE AUTOLEUCEL reports
3
Deaths
11
Hospitalizations

How Dangerous Is Nausea From BREXUCABTAGENE AUTOLEUCEL?

Of the 30 reports, 3 (10.0%) resulted in death, 11 (36.7%) required hospitalization.

Is Nausea Listed in the Official Label?

Yes, Nausea is listed as a known adverse reaction in the official FDA drug label for BREXUCABTAGENE AUTOLEUCEL.

What Other Side Effects Does BREXUCABTAGENE AUTOLEUCEL Cause?

Cytokine release syndrome (827) Immune effector cell-associated neurotoxicity syndrome (529) Neurotoxicity (192) Death (153) Pyrexia (119) Hypotension (109) Disease progression (93) Fatigue (86) Febrile neutropenia (69) Confusional state (63)

What Other Drugs Cause Nausea?

APREMILAST (21,352) ADALIMUMAB (19,299) METHOTREXATE (18,715) ETANERCEPT (12,174) TREPROSTINIL (10,320) RITUXIMAB (10,250) SEMAGLUTIDE (10,036) TIRZEPATIDE (10,018) LENALIDOMIDE (9,206) DULAGLUTIDE (9,137)

Which BREXUCABTAGENE AUTOLEUCEL Alternatives Have Lower Nausea Risk?

BREXUCABTAGENE AUTOLEUCEL vs BRIGATINIB BREXUCABTAGENE AUTOLEUCEL vs BRILINTA BREXUCABTAGENE AUTOLEUCEL vs BRILIQUE BREXUCABTAGENE AUTOLEUCEL vs BRIMONIDINE BREXUCABTAGENE AUTOLEUCEL vs BRIMONIDINE\BRINZOLAMIDE

Related Pages

BREXUCABTAGENE AUTOLEUCEL Full Profile All Nausea Reports All Drugs Causing Nausea BREXUCABTAGENE AUTOLEUCEL Demographics