Does BREXPIPRAZOLE Cause Dyskinesia? 204 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 204 reports of Dyskinesia have been filed in association with BREXPIPRAZOLE (Rexulti). This represents 1.5% of all adverse event reports for BREXPIPRAZOLE.
204
Reports of Dyskinesia with BREXPIPRAZOLE
1.5%
of all BREXPIPRAZOLE reports
1
Deaths
17
Hospitalizations
How Dangerous Is Dyskinesia From BREXPIPRAZOLE?
Of the 204 reports, 1 (0.5%) resulted in death, 17 (8.3%) required hospitalization, and 2 (1.0%) were considered life-threatening.
Is Dyskinesia Listed in the Official Label?
Yes, Dyskinesia 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)
Akathisia (807)
Drug ineffective (730)
Tardive dyskinesia (558)
Tremor (552)
Anxiety (475)
Product use issue (434)
Suicidal ideation (427)
What Other Drugs Cause Dyskinesia?
CARBIDOPA\LEVODOPA (5,368)
QUETIAPINE (1,529)
ARIPIPRAZOLE (1,496)
RISPERIDONE (1,363)
OLANZAPINE (1,060)
CLOZAPINE (890)
PALIPERIDONE (794)
LURASIDONE (791)
VALBENAZINE (772)
SERTRALINE (597)
Which BREXPIPRAZOLE Alternatives Have Lower Dyskinesia Risk?
BREXPIPRAZOLE vs BREXUCABTAGENE AUTOLEUCEL
BREXPIPRAZOLE vs BRIGATINIB
BREXPIPRAZOLE vs BRILINTA
BREXPIPRAZOLE vs BRILIQUE
BREXPIPRAZOLE vs BRIMONIDINE