Does BREXPIPRAZOLE Cause Intentional product misuse? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Intentional product misuse have been filed in association with BREXPIPRAZOLE (Rexulti). This represents 0.1% of all adverse event reports for BREXPIPRAZOLE.
12
Reports of Intentional product misuse with BREXPIPRAZOLE
0.1%
of all BREXPIPRAZOLE reports
1
Deaths
7
Hospitalizations
How Dangerous Is Intentional product misuse From BREXPIPRAZOLE?
Of the 12 reports, 1 (8.3%) resulted in death, 7 (58.3%) required hospitalization.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BREXPIPRAZOLE. However, 12 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which BREXPIPRAZOLE Alternatives Have Lower Intentional product misuse Risk?
BREXPIPRAZOLE vs BREXUCABTAGENE AUTOLEUCEL
BREXPIPRAZOLE vs BRIGATINIB
BREXPIPRAZOLE vs BRILINTA
BREXPIPRAZOLE vs BRILIQUE
BREXPIPRAZOLE vs BRIMONIDINE