Does DULOXETINE Cause Product prescribing error? 115 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 115 reports of Product prescribing error have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 0.2% of all adverse event reports for DULOXETINE.
115
Reports of Product prescribing error with DULOXETINE
0.2%
of all DULOXETINE reports
3
Deaths
69
Hospitalizations
How Dangerous Is Product prescribing error From DULOXETINE?
Of the 115 reports, 3 (2.6%) resulted in death, 69 (60.0%) required hospitalization, and 2 (1.7%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 115 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 prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which DULOXETINE Alternatives Have Lower Product prescribing error Risk?
DULOXETINE vs DUPILUMAB
DULOXETINE vs DURAGESIC
DULOXETINE vs DUROGESIC
DULOXETINE vs DUROTEP MT
DULOXETINE vs DURVALUMAB