Does VORTIOXETINE HYDROBROMIDE Cause Presyncope? 43 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 43 reports of Presyncope have been filed in association with VORTIOXETINE HYDROBROMIDE (Trintellix). This represents 0.3% of all adverse event reports for VORTIOXETINE HYDROBROMIDE.
43
Reports of Presyncope with VORTIOXETINE HYDROBROMIDE
0.3%
of all VORTIOXETINE HYDROBROMIDE reports
27
Deaths
2
Hospitalizations
How Dangerous Is Presyncope From VORTIOXETINE HYDROBROMIDE?
Of the 43 reports, 27 (62.8%) resulted in death, 2 (4.7%) required hospitalization, and 4 (9.3%) were considered life-threatening.
Is Presyncope Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VORTIOXETINE HYDROBROMIDE. However, 43 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 Presyncope?
TREPROSTINIL (585)
BISOPROLOL (485)
LEVONORGESTREL (429)
ADALIMUMAB (420)
AMBRISENTAN (407)
ASPIRIN (370)
TAMSULOSIN (361)
FUROSEMIDE (348)
SERTRALINE (337)
ETANERCEPT (334)
Which VORTIOXETINE HYDROBROMIDE Alternatives Have Lower Presyncope Risk?
VORTIOXETINE HYDROBROMIDE vs VOSORITIDE
VORTIOXETINE HYDROBROMIDE vs VOTRIENT
VORTIOXETINE HYDROBROMIDE vs VOXELOTOR
VORTIOXETINE HYDROBROMIDE vs VUTRISIRAN
VORTIOXETINE HYDROBROMIDE vs VX-950