Does BREXPIPRAZOLE Cause Akathisia? 807 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 807 reports of Akathisia have been filed in association with BREXPIPRAZOLE (Rexulti). This represents 6.1% of all adverse event reports for BREXPIPRAZOLE.
807
Reports of Akathisia with BREXPIPRAZOLE
6.1%
of all BREXPIPRAZOLE reports
11
Deaths
53
Hospitalizations
How Dangerous Is Akathisia From BREXPIPRAZOLE?
Of the 807 reports, 11 (1.4%) resulted in death, 53 (6.6%) required hospitalization, and 15 (1.9%) were considered life-threatening.
Is Akathisia Listed in the Official Label?
Yes, Akathisia is listed as a known adverse reaction in the official FDA drug label for BREXPIPRAZOLE.
What Other Side Effects Does BREXPIPRAZOLE Cause?
Weight increased (1,589)
Product use in unapproved indication (1,188)
Off label use (937)
Drug ineffective (730)
Tardive dyskinesia (558)
Tremor (552)
Anxiety (475)
Product use issue (434)
Suicidal ideation (427)
Depression (413)
What Other Drugs Cause Akathisia?
ARIPIPRAZOLE (2,107)
OLANZAPINE (1,230)
RISPERIDONE (1,150)
QUETIAPINE (925)
PALIPERIDONE (607)
LURASIDONE (552)
HALOPERIDOL (551)
SERTRALINE (498)
CLOZAPINE (474)
FLUOXETINE (410)
Which BREXPIPRAZOLE Alternatives Have Lower Akathisia Risk?
BREXPIPRAZOLE vs BREXUCABTAGENE AUTOLEUCEL
BREXPIPRAZOLE vs BRIGATINIB
BREXPIPRAZOLE vs BRILINTA
BREXPIPRAZOLE vs BRILIQUE
BREXPIPRAZOLE vs BRIMONIDINE