Does VORTIOXETINE HYDROBROMIDE Cause Adverse event? 79 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 79 reports of Adverse event have been filed in association with VORTIOXETINE HYDROBROMIDE (Trintellix). This represents 0.6% of all adverse event reports for VORTIOXETINE HYDROBROMIDE.
79
Reports of Adverse event with VORTIOXETINE HYDROBROMIDE
0.6%
of all VORTIOXETINE HYDROBROMIDE reports
1
Deaths
9
Hospitalizations
How Dangerous Is Adverse event From VORTIOXETINE HYDROBROMIDE?
Of the 79 reports, 1 (1.3%) resulted in death, 9 (11.4%) required hospitalization.
Is Adverse event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VORTIOXETINE HYDROBROMIDE. However, 79 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 Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which VORTIOXETINE HYDROBROMIDE Alternatives Have Lower Adverse event Risk?
VORTIOXETINE HYDROBROMIDE vs VOSORITIDE
VORTIOXETINE HYDROBROMIDE vs VOTRIENT
VORTIOXETINE HYDROBROMIDE vs VOXELOTOR
VORTIOXETINE HYDROBROMIDE vs VUTRISIRAN
VORTIOXETINE HYDROBROMIDE vs VX-950