Does VORTIOXETINE HYDROBROMIDE Cause Withdrawal syndrome? 74 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 74 reports of Withdrawal syndrome have been filed in association with VORTIOXETINE HYDROBROMIDE (Trintellix). This represents 0.5% of all adverse event reports for VORTIOXETINE HYDROBROMIDE.
74
Reports of Withdrawal syndrome with VORTIOXETINE HYDROBROMIDE
0.5%
of all VORTIOXETINE HYDROBROMIDE reports
0
Deaths
7
Hospitalizations
How Dangerous Is Withdrawal syndrome From VORTIOXETINE HYDROBROMIDE?
Of the 74 reports, 7 (9.5%) required hospitalization, and 6 (8.1%) were considered life-threatening.
Is Withdrawal syndrome Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VORTIOXETINE HYDROBROMIDE. However, 74 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 Withdrawal syndrome?
ACETAMINOPHEN\OXYCODONE (4,046)
PREGABALIN (3,329)
OXYCODONE (2,798)
ACETAMINOPHEN\HYDROCODONE (2,636)
FENTANYL (1,948)
MORPHINE (1,674)
TRAMADOL (1,582)
VENLAFAXINE (1,516)
DULOXETINE (1,328)
BUPRENORPHINE (1,266)
Which VORTIOXETINE HYDROBROMIDE Alternatives Have Lower Withdrawal syndrome Risk?
VORTIOXETINE HYDROBROMIDE vs VOSORITIDE
VORTIOXETINE HYDROBROMIDE vs VOTRIENT
VORTIOXETINE HYDROBROMIDE vs VOXELOTOR
VORTIOXETINE HYDROBROMIDE vs VUTRISIRAN
VORTIOXETINE HYDROBROMIDE vs VX-950