Does BREXUCABTAGENE AUTOLEUCEL Cause Syncope? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Syncope have been filed in association with BREXUCABTAGENE AUTOLEUCEL (TECARTUS). This represents 0.3% of all adverse event reports for BREXUCABTAGENE AUTOLEUCEL.
6
Reports of Syncope with BREXUCABTAGENE AUTOLEUCEL
0.3%
of all BREXUCABTAGENE AUTOLEUCEL reports
0
Deaths
5
Hospitalizations
How Dangerous Is Syncope From BREXUCABTAGENE AUTOLEUCEL?
Of the 6 reports, 5 (83.3%) required hospitalization.
Is Syncope Listed in the Official Label?
Yes, Syncope 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 Syncope?
AMBRISENTAN (2,140)
TREPROSTINIL (1,908)
ADALIMUMAB (1,795)
FUROSEMIDE (1,431)
LENALIDOMIDE (1,280)
BISOPROLOL (1,279)
METOPROLOL (1,251)
AMLODIPINE (1,224)
ASPIRIN (1,193)
SACUBITRIL\VALSARTAN (1,163)
Which BREXUCABTAGENE AUTOLEUCEL Alternatives Have Lower Syncope Risk?
BREXUCABTAGENE AUTOLEUCEL vs BRIGATINIB
BREXUCABTAGENE AUTOLEUCEL vs BRILINTA
BREXUCABTAGENE AUTOLEUCEL vs BRILIQUE
BREXUCABTAGENE AUTOLEUCEL vs BRIMONIDINE
BREXUCABTAGENE AUTOLEUCEL vs BRIMONIDINE\BRINZOLAMIDE