Does VORTIOXETINE HYDROBROMIDE Cause Condition aggravated? 222 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 222 reports of Condition aggravated have been filed in association with VORTIOXETINE HYDROBROMIDE (Trintellix). This represents 1.6% of all adverse event reports for VORTIOXETINE HYDROBROMIDE.
222
Reports of Condition aggravated with VORTIOXETINE HYDROBROMIDE
1.6%
of all VORTIOXETINE HYDROBROMIDE reports
4
Deaths
52
Hospitalizations
How Dangerous Is Condition aggravated From VORTIOXETINE HYDROBROMIDE?
Of the 222 reports, 4 (1.8%) resulted in death, 52 (23.4%) required hospitalization, and 7 (3.2%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VORTIOXETINE HYDROBROMIDE. However, 222 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which VORTIOXETINE HYDROBROMIDE Alternatives Have Lower Condition aggravated Risk?
VORTIOXETINE HYDROBROMIDE vs VOSORITIDE
VORTIOXETINE HYDROBROMIDE vs VOTRIENT
VORTIOXETINE HYDROBROMIDE vs VOXELOTOR
VORTIOXETINE HYDROBROMIDE vs VUTRISIRAN
VORTIOXETINE HYDROBROMIDE vs VX-950