Does BREXPIPRAZOLE Cause Condition aggravated? 232 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 232 reports of Condition aggravated have been filed in association with BREXPIPRAZOLE (Rexulti). This represents 1.8% of all adverse event reports for BREXPIPRAZOLE.
232
Reports of Condition aggravated with BREXPIPRAZOLE
1.8%
of all BREXPIPRAZOLE reports
1
Deaths
101
Hospitalizations
How Dangerous Is Condition aggravated From BREXPIPRAZOLE?
Of the 232 reports, 1 (0.4%) resulted in death, 101 (43.5%) required hospitalization.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BREXPIPRAZOLE. However, 232 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which BREXPIPRAZOLE Alternatives Have Lower Condition aggravated Risk?
BREXPIPRAZOLE vs BREXUCABTAGENE AUTOLEUCEL
BREXPIPRAZOLE vs BRIGATINIB
BREXPIPRAZOLE vs BRILINTA
BREXPIPRAZOLE vs BRILIQUE
BREXPIPRAZOLE vs BRIMONIDINE