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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 BREXPIPRAZOLE Cause Sepsis? 13 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Sepsis have been filed in association with BREXPIPRAZOLE (Rexulti). This represents 0.1% of all adverse event reports for BREXPIPRAZOLE.

13
Reports of Sepsis with BREXPIPRAZOLE
0.1%
of all BREXPIPRAZOLE reports
7
Deaths
7
Hospitalizations

How Dangerous Is Sepsis From BREXPIPRAZOLE?

Of the 13 reports, 7 (53.8%) resulted in death, 7 (53.8%) required hospitalization, and 3 (23.1%) were considered life-threatening.

Is Sepsis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BREXPIPRAZOLE. However, 13 reports have been filed with the FAERS database.

What Other Side Effects Does BREXPIPRAZOLE Cause?

Weight increased (1,589) Product use in unapproved indication (1,188) Off label use (937) Akathisia (807) Drug ineffective (730) Tardive dyskinesia (558) Tremor (552) Anxiety (475) Product use issue (434) Suicidal ideation (427)

What Other Drugs Cause Sepsis?

RITUXIMAB (4,043) CYCLOPHOSPHAMIDE (4,041) METHOTREXATE (3,933) ADALIMUMAB (3,169) DEXAMETHASONE (3,150) LENALIDOMIDE (2,956) VINCRISTINE (2,791) DOXORUBICIN (2,740) PREDNISONE (2,634) PREDNISOLONE (2,281)

Which BREXPIPRAZOLE Alternatives Have Lower Sepsis Risk?

BREXPIPRAZOLE vs BREXUCABTAGENE AUTOLEUCEL BREXPIPRAZOLE vs BRIGATINIB BREXPIPRAZOLE vs BRILINTA BREXPIPRAZOLE vs BRILIQUE BREXPIPRAZOLE vs BRIMONIDINE

Related Pages

BREXPIPRAZOLE Full Profile All Sepsis Reports All Drugs Causing Sepsis BREXPIPRAZOLE Demographics