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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does BREXPIPRAZOLE Cause Wrong technique in product usage process? 199 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 199 reports of Wrong technique in product usage process have been filed in association with BREXPIPRAZOLE (Rexulti). This represents 1.5% of all adverse event reports for BREXPIPRAZOLE.

199
Reports of Wrong technique in product usage process with BREXPIPRAZOLE
1.5%
of all BREXPIPRAZOLE reports
1
Deaths
6
Hospitalizations

How Dangerous Is Wrong technique in product usage process From BREXPIPRAZOLE?

Of the 199 reports, 1 (0.5%) resulted in death, 6 (3.0%) required hospitalization.

Is Wrong technique in product usage process Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BREXPIPRAZOLE. However, 199 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 Wrong technique in product usage process?

EVOLOCUMAB (21,664) ALBUTEROL (17,114) ADALIMUMAB (11,766) PEGFILGRASTIM (10,217) ETANERCEPT (9,835) ERENUMAB-AOOE (9,359) SACUBITRIL\VALSARTAN (8,022) LEUPROLIDE (5,062) FENTANYL (2,812) SEMAGLUTIDE (2,538)

Which BREXPIPRAZOLE Alternatives Have Lower Wrong technique in product usage process Risk?

BREXPIPRAZOLE vs BREXUCABTAGENE AUTOLEUCEL BREXPIPRAZOLE vs BRIGATINIB BREXPIPRAZOLE vs BRILINTA BREXPIPRAZOLE vs BRILIQUE BREXPIPRAZOLE vs BRIMONIDINE

Related Pages

BREXPIPRAZOLE Full Profile All Wrong technique in product usage process Reports All Drugs Causing Wrong technique in product usage process BREXPIPRAZOLE Demographics