Does VORTIOXETINE Cause Condition aggravated? 98 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 98 reports of Condition aggravated have been filed in association with VORTIOXETINE. This represents 4.0% of all adverse event reports for VORTIOXETINE.
98
Reports of Condition aggravated with VORTIOXETINE
4.0%
of all VORTIOXETINE reports
2
Deaths
82
Hospitalizations
How Dangerous Is Condition aggravated From VORTIOXETINE?
Of the 98 reports, 2 (2.0%) resulted in death, 82 (83.7%) required hospitalization, and 2 (2.0%) 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. However, 98 reports have been filed with the FAERS database.
What Other Side Effects Does VORTIOXETINE Cause?
Suicidal ideation (319)
Nausea (264)
Drug ineffective (245)
Dizziness (218)
Insomnia (211)
Fall (206)
Headache (193)
Pruritus (189)
Tachycardia (182)
Diarrhoea (181)
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 Alternatives Have Lower Condition aggravated Risk?
VORTIOXETINE vs VORTIOXETINE HYDROBROMIDE
VORTIOXETINE vs VOSORITIDE
VORTIOXETINE vs VOTRIENT
VORTIOXETINE vs VOXELOTOR
VORTIOXETINE vs VUTRISIRAN