Does VORTIOXETINE HYDROBROMIDE Cause Product dose omission issue? 63 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 63 reports of Product dose omission issue have been filed in association with VORTIOXETINE HYDROBROMIDE (Trintellix). This represents 0.5% of all adverse event reports for VORTIOXETINE HYDROBROMIDE.
63
Reports of Product dose omission issue with VORTIOXETINE HYDROBROMIDE
0.5%
of all VORTIOXETINE HYDROBROMIDE reports
0
Deaths
5
Hospitalizations
How Dangerous Is Product dose omission issue From VORTIOXETINE HYDROBROMIDE?
Of the 63 reports, 5 (7.9%) required hospitalization.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VORTIOXETINE HYDROBROMIDE. However, 63 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 dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which VORTIOXETINE HYDROBROMIDE Alternatives Have Lower Product dose omission issue Risk?
VORTIOXETINE HYDROBROMIDE vs VOSORITIDE
VORTIOXETINE HYDROBROMIDE vs VOTRIENT
VORTIOXETINE HYDROBROMIDE vs VOXELOTOR
VORTIOXETINE HYDROBROMIDE vs VUTRISIRAN
VORTIOXETINE HYDROBROMIDE vs VX-950