Does DULOXETINE Cause Unevaluable event? 201 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 201 reports of Unevaluable event have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 0.4% of all adverse event reports for DULOXETINE.
201
Reports of Unevaluable event with DULOXETINE
0.4%
of all DULOXETINE reports
4
Deaths
18
Hospitalizations
How Dangerous Is Unevaluable event From DULOXETINE?
Of the 201 reports, 4 (2.0%) resulted in death, 18 (9.0%) required hospitalization, and 3 (1.5%) were considered life-threatening.
Is Unevaluable event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 201 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 Unevaluable event?
ADALIMUMAB (4,242)
ETANERCEPT (3,902)
LENALIDOMIDE (3,331)
OXYCODONE (3,145)
AMBRISENTAN (2,336)
SODIUM OXYBATE (2,328)
CARBIDOPA\LEVODOPA (1,632)
DUPILUMAB (1,410)
MORPHINE (1,161)
ACETAMINOPHEN\HYDROCODONE (1,118)
Which DULOXETINE Alternatives Have Lower Unevaluable event Risk?
DULOXETINE vs DUPILUMAB
DULOXETINE vs DURAGESIC
DULOXETINE vs DUROGESIC
DULOXETINE vs DUROTEP MT
DULOXETINE vs DURVALUMAB