Does BREXPIPRAZOLE Cause Incorrect dose administered? 306 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 306 reports of Incorrect dose administered have been filed in association with BREXPIPRAZOLE (Rexulti). This represents 2.3% of all adverse event reports for BREXPIPRAZOLE.
306
Reports of Incorrect dose administered with BREXPIPRAZOLE
2.3%
of all BREXPIPRAZOLE reports
9
Deaths
24
Hospitalizations
How Dangerous Is Incorrect dose administered From BREXPIPRAZOLE?
Of the 306 reports, 9 (2.9%) resulted in death, 24 (7.8%) required hospitalization, and 3 (1.0%) were considered life-threatening.
Is Incorrect dose administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BREXPIPRAZOLE. However, 306 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 Incorrect dose administered?
TIRZEPATIDE (23,301)
ADALIMUMAB (14,000)
DUPILUMAB (9,907)
RANITIDINE (9,337)
INSULIN LISPRO (8,318)
ACETAMINOPHEN (5,316)
DULAGLUTIDE (5,207)
SECUKINUMAB (4,524)
INSULIN GLARGINE (3,070)
SOMATROPIN (2,772)
Which BREXPIPRAZOLE Alternatives Have Lower Incorrect dose administered Risk?
BREXPIPRAZOLE vs BREXUCABTAGENE AUTOLEUCEL
BREXPIPRAZOLE vs BRIGATINIB
BREXPIPRAZOLE vs BRILINTA
BREXPIPRAZOLE vs BRILIQUE
BREXPIPRAZOLE vs BRIMONIDINE