Does DULOXETINE Cause Product use issue? 297 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 297 reports of Product use issue have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 0.6% of all adverse event reports for DULOXETINE.
297
Reports of Product use issue with DULOXETINE
0.6%
of all DULOXETINE reports
9
Deaths
141
Hospitalizations
How Dangerous Is Product use issue From DULOXETINE?
Of the 297 reports, 9 (3.0%) resulted in death, 141 (47.5%) required hospitalization, and 11 (3.7%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 297 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 Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which DULOXETINE Alternatives Have Lower Product use issue Risk?
DULOXETINE vs DUPILUMAB
DULOXETINE vs DURAGESIC
DULOXETINE vs DUROGESIC
DULOXETINE vs DUROTEP MT
DULOXETINE vs DURVALUMAB