Does DULOXETINE Cause Intentional product misuse? 1,418 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,418 reports of Intentional product misuse have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 2.7% of all adverse event reports for DULOXETINE.
1,418
Reports of Intentional product misuse with DULOXETINE
2.7%
of all DULOXETINE reports
65
Deaths
179
Hospitalizations
How Dangerous Is Intentional product misuse From DULOXETINE?
Of the 1,418 reports, 65 (4.6%) resulted in death, 179 (12.6%) required hospitalization, and 24 (1.7%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 1,418 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which DULOXETINE Alternatives Have Lower Intentional product misuse Risk?
DULOXETINE vs DUPILUMAB
DULOXETINE vs DURAGESIC
DULOXETINE vs DUROGESIC
DULOXETINE vs DUROTEP MT
DULOXETINE vs DURVALUMAB