Does BREXPIPRAZOLE Cause Dyspnoea? 102 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 102 reports of Dyspnoea have been filed in association with BREXPIPRAZOLE (Rexulti). This represents 0.8% of all adverse event reports for BREXPIPRAZOLE.
102
Reports of Dyspnoea with BREXPIPRAZOLE
0.8%
of all BREXPIPRAZOLE reports
4
Deaths
17
Hospitalizations
How Dangerous Is Dyspnoea From BREXPIPRAZOLE?
Of the 102 reports, 4 (3.9%) resulted in death, 17 (16.7%) required hospitalization, and 3 (2.9%) were considered life-threatening.
Is Dyspnoea Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BREXPIPRAZOLE. However, 102 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 Dyspnoea?
ALBUTEROL (21,856)
TREPROSTINIL (16,348)
AMBRISENTAN (13,367)
PREDNISONE (12,830)
BUDESONIDE\FORMOTEROL (11,158)
TIOTROPIUM (10,863)
ADALIMUMAB (10,547)
DUPILUMAB (10,310)
FLUTICASONE\SALMETEROL (9,783)
MEPOLIZUMAB (9,192)
Which BREXPIPRAZOLE Alternatives Have Lower Dyspnoea Risk?
BREXPIPRAZOLE vs BREXUCABTAGENE AUTOLEUCEL
BREXPIPRAZOLE vs BRIGATINIB
BREXPIPRAZOLE vs BRILINTA
BREXPIPRAZOLE vs BRILIQUE
BREXPIPRAZOLE vs BRIMONIDINE