Does BREXUCABTAGENE AUTOLEUCEL Cause Hypoxia? 43 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 43 reports of Hypoxia have been filed in association with BREXUCABTAGENE AUTOLEUCEL (TECARTUS). This represents 2.5% of all adverse event reports for BREXUCABTAGENE AUTOLEUCEL.
43
Reports of Hypoxia with BREXUCABTAGENE AUTOLEUCEL
2.5%
of all BREXUCABTAGENE AUTOLEUCEL reports
9
Deaths
22
Hospitalizations
How Dangerous Is Hypoxia From BREXUCABTAGENE AUTOLEUCEL?
Of the 43 reports, 9 (20.9%) resulted in death, 22 (51.2%) required hospitalization, and 9 (20.9%) were considered life-threatening.
Is Hypoxia Listed in the Official Label?
Yes, Hypoxia 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 Hypoxia?
TREPROSTINIL (1,322)
PREDNISONE (898)
MACITENTAN (845)
ALBUTEROL (763)
CYCLOPHOSPHAMIDE (749)
PACLITAXEL (684)
DEXAMETHASONE (628)
AMBRISENTAN (613)
TIOTROPIUM (582)
ACETAMINOPHEN (545)
Which BREXUCABTAGENE AUTOLEUCEL Alternatives Have Lower Hypoxia Risk?
BREXUCABTAGENE AUTOLEUCEL vs BRIGATINIB
BREXUCABTAGENE AUTOLEUCEL vs BRILINTA
BREXUCABTAGENE AUTOLEUCEL vs BRILIQUE
BREXUCABTAGENE AUTOLEUCEL vs BRIMONIDINE
BREXUCABTAGENE AUTOLEUCEL vs BRIMONIDINE\BRINZOLAMIDE