Does BREXPIPRAZOLE Cause Tardive dyskinesia? 558 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 558 reports of Tardive dyskinesia have been filed in association with BREXPIPRAZOLE (Rexulti). This represents 4.2% of all adverse event reports for BREXPIPRAZOLE.
558
Reports of Tardive dyskinesia with BREXPIPRAZOLE
4.2%
of all BREXPIPRAZOLE reports
0
Deaths
26
Hospitalizations
How Dangerous Is Tardive dyskinesia From BREXPIPRAZOLE?
Of the 558 reports, 26 (4.7%) required hospitalization, and 4 (0.7%) were considered life-threatening.
Is Tardive dyskinesia Listed in the Official Label?
Yes, Tardive 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)
Tremor (552)
Anxiety (475)
Product use issue (434)
Suicidal ideation (427)
Depression (413)
What Other Drugs Cause Tardive dyskinesia?
ARIPIPRAZOLE (1,399)
VALBENAZINE (1,383)
RISPERIDONE (996)
QUETIAPINE (709)
OLANZAPINE (558)
LURASIDONE (509)
METOCLOPRAMIDE (465)
PALIPERIDONE (410)
CLOZAPINE (321)
CARIPRAZINE (305)
Which BREXPIPRAZOLE Alternatives Have Lower Tardive dyskinesia Risk?
BREXPIPRAZOLE vs BREXUCABTAGENE AUTOLEUCEL
BREXPIPRAZOLE vs BRIGATINIB
BREXPIPRAZOLE vs BRILINTA
BREXPIPRAZOLE vs BRILIQUE
BREXPIPRAZOLE vs BRIMONIDINE