Does DULOXETINE Cause Off label use? 3,711 Reports in FDA Database
Sharpen Your Memory & Focus Naturally
NeuroZoom — 35 clinically studied ingredients. No stimulants. Pure brain support.
According to the FDA Adverse Event Reporting System (FAERS), 3,711 reports of Off label use have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 7.1% of all adverse event reports for DULOXETINE.
3,711
Reports of Off label use with DULOXETINE
7.1%
of all DULOXETINE reports
82
Deaths
615
Hospitalizations
How Dangerous Is Off label use From DULOXETINE?
Of the 3,711 reports, 82 (2.2%) resulted in death, 615 (16.6%) required hospitalization, and 81 (2.2%) were considered life-threatening.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 3,711 reports have been filed with the FAERS database.
What Other Side Effects Does DULOXETINE Cause?
Nausea (7,355)
Dizziness (6,983)
Drug withdrawal syndrome (6,503)
Headache (5,541)
Fatigue (5,309)
Insomnia (5,270)
Anxiety (4,973)
Paraesthesia (4,854)
Drug ineffective (4,829)
Hyperhidrosis (4,101)
What Other Drugs Cause Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)
Which DULOXETINE Alternatives Have Lower Off label use Risk?
DULOXETINE vs DUPILUMAB
DULOXETINE vs DURAGESIC
DULOXETINE vs DUROGESIC
DULOXETINE vs DUROTEP MT
DULOXETINE vs DURVALUMAB