Does BREXUCABTAGENE AUTOLEUCEL Cause Hypotension? 109 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 109 reports of Hypotension have been filed in association with BREXUCABTAGENE AUTOLEUCEL (TECARTUS). This represents 6.2% of all adverse event reports for BREXUCABTAGENE AUTOLEUCEL.
109
Reports of Hypotension with BREXUCABTAGENE AUTOLEUCEL
6.2%
of all BREXUCABTAGENE AUTOLEUCEL reports
27
Deaths
63
Hospitalizations
How Dangerous Is Hypotension From BREXUCABTAGENE AUTOLEUCEL?
Of the 109 reports, 27 (24.8%) resulted in death, 63 (57.8%) required hospitalization, and 21 (19.3%) were considered life-threatening.
Is Hypotension Listed in the Official Label?
Yes, Hypotension 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)
Disease progression (93)
Fatigue (86)
Febrile neutropenia (69)
Confusional state (63)
Encephalopathy (53)
What Other Drugs Cause Hypotension?
SACUBITRIL\VALSARTAN (11,718)
AMLODIPINE (6,504)
CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (4,694)
FUROSEMIDE (4,468)
TREPROSTINIL (4,412)
METOPROLOL (3,213)
RITUXIMAB (3,208)
METFORMIN (3,116)
LENALIDOMIDE (2,920)
ACETAMINOPHEN (2,817)
Which BREXUCABTAGENE AUTOLEUCEL Alternatives Have Lower Hypotension Risk?
BREXUCABTAGENE AUTOLEUCEL vs BRIGATINIB
BREXUCABTAGENE AUTOLEUCEL vs BRILINTA
BREXUCABTAGENE AUTOLEUCEL vs BRILIQUE
BREXUCABTAGENE AUTOLEUCEL vs BRIMONIDINE
BREXUCABTAGENE AUTOLEUCEL vs BRIMONIDINE\BRINZOLAMIDE