Does BREXPIPRAZOLE Cause Unevaluable event? 45 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 45 reports of Unevaluable event have been filed in association with BREXPIPRAZOLE (Rexulti). This represents 0.3% of all adverse event reports for BREXPIPRAZOLE.
45
Reports of Unevaluable event with BREXPIPRAZOLE
0.3%
of all BREXPIPRAZOLE reports
2
Deaths
5
Hospitalizations
How Dangerous Is Unevaluable event From BREXPIPRAZOLE?
Of the 45 reports, 2 (4.4%) resulted in death, 5 (11.1%) required hospitalization, and 2 (4.4%) were considered life-threatening.
Is Unevaluable event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BREXPIPRAZOLE. However, 45 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 Unevaluable event?
ADALIMUMAB (4,242)
ETANERCEPT (3,902)
LENALIDOMIDE (3,331)
OXYCODONE (3,145)
AMBRISENTAN (2,336)
SODIUM OXYBATE (2,328)
CARBIDOPA\LEVODOPA (1,632)
DUPILUMAB (1,410)
MORPHINE (1,161)
ACETAMINOPHEN\HYDROCODONE (1,118)
Which BREXPIPRAZOLE Alternatives Have Lower Unevaluable event Risk?
BREXPIPRAZOLE vs BREXUCABTAGENE AUTOLEUCEL
BREXPIPRAZOLE vs BRIGATINIB
BREXPIPRAZOLE vs BRILINTA
BREXPIPRAZOLE vs BRILIQUE
BREXPIPRAZOLE vs BRIMONIDINE