Does VORTIOXETINE HYDROBROMIDE Cause Off label use? 468 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 468 reports of Off label use have been filed in association with VORTIOXETINE HYDROBROMIDE (Trintellix). This represents 3.4% of all adverse event reports for VORTIOXETINE HYDROBROMIDE.
468
Reports of Off label use with VORTIOXETINE HYDROBROMIDE
3.4%
of all VORTIOXETINE HYDROBROMIDE reports
13
Deaths
41
Hospitalizations
How Dangerous Is Off label use From VORTIOXETINE HYDROBROMIDE?
Of the 468 reports, 13 (2.8%) resulted in death, 41 (8.8%) required hospitalization, and 6 (1.3%) were considered life-threatening.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VORTIOXETINE HYDROBROMIDE. However, 468 reports have been filed with the FAERS database.
What Other Side Effects Does VORTIOXETINE HYDROBROMIDE Cause?
Nausea (2,062)
Anxiety (861)
Vomiting (811)
Suicidal ideation (742)
Headache (738)
Fatigue (697)
Drug ineffective (693)
Pruritus (653)
Insomnia (636)
Feeling abnormal (620)
What Other Drugs Cause Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)
Which VORTIOXETINE HYDROBROMIDE Alternatives Have Lower Off label use Risk?
VORTIOXETINE HYDROBROMIDE vs VOSORITIDE
VORTIOXETINE HYDROBROMIDE vs VOTRIENT
VORTIOXETINE HYDROBROMIDE vs VOXELOTOR
VORTIOXETINE HYDROBROMIDE vs VUTRISIRAN
VORTIOXETINE HYDROBROMIDE vs VX-950