Does VORTIOXETINE HYDROBROMIDE Cause Product use issue? 130 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 130 reports of Product use issue have been filed in association with VORTIOXETINE HYDROBROMIDE (Trintellix). This represents 1.0% of all adverse event reports for VORTIOXETINE HYDROBROMIDE.
130
Reports of Product use issue with VORTIOXETINE HYDROBROMIDE
1.0%
of all VORTIOXETINE HYDROBROMIDE reports
1
Deaths
13
Hospitalizations
How Dangerous Is Product use issue From VORTIOXETINE HYDROBROMIDE?
Of the 130 reports, 1 (0.8%) resulted in death, 13 (10.0%) required hospitalization, and 3 (2.3%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VORTIOXETINE HYDROBROMIDE. However, 130 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 Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which VORTIOXETINE HYDROBROMIDE Alternatives Have Lower Product use issue Risk?
VORTIOXETINE HYDROBROMIDE vs VOSORITIDE
VORTIOXETINE HYDROBROMIDE vs VOTRIENT
VORTIOXETINE HYDROBROMIDE vs VOXELOTOR
VORTIOXETINE HYDROBROMIDE vs VUTRISIRAN
VORTIOXETINE HYDROBROMIDE vs VX-950