Does BREXPIPRAZOLE Cause Hyperprolactinaemia? 35 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 35 reports of Hyperprolactinaemia have been filed in association with BREXPIPRAZOLE (Rexulti). This represents 0.3% of all adverse event reports for BREXPIPRAZOLE.
35
Reports of Hyperprolactinaemia with BREXPIPRAZOLE
0.3%
of all BREXPIPRAZOLE reports
0
Deaths
10
Hospitalizations
How Dangerous Is Hyperprolactinaemia From BREXPIPRAZOLE?
Of the 35 reports, 10 (28.6%) required hospitalization.
Is Hyperprolactinaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BREXPIPRAZOLE. However, 35 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 Hyperprolactinaemia?
RISPERIDONE (4,124)
PALIPERIDONE (1,427)
OLANZAPINE (520)
ARIPIPRAZOLE (459)
QUETIAPINE (331)
HALOPERIDOL (214)
CLOZAPINE (157)
AMISULPRIDE (135)
SERTRALINE (120)
LITHIUM (76)
Which BREXPIPRAZOLE Alternatives Have Lower Hyperprolactinaemia Risk?
BREXPIPRAZOLE vs BREXUCABTAGENE AUTOLEUCEL
BREXPIPRAZOLE vs BRIGATINIB
BREXPIPRAZOLE vs BRILINTA
BREXPIPRAZOLE vs BRILIQUE
BREXPIPRAZOLE vs BRIMONIDINE