Does DULOXETINE Cause Wrong patient received product? 26 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), 26 reports of Wrong patient received product have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 0.1% of all adverse event reports for DULOXETINE.
26
Reports of Wrong patient received product with DULOXETINE
0.1%
of all DULOXETINE reports
10
Deaths
10
Hospitalizations
How Dangerous Is Wrong patient received product From DULOXETINE?
Of the 26 reports, 10 (38.5%) resulted in death, 10 (38.5%) required hospitalization.
Is Wrong patient received product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 26 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 Wrong patient received product?
INSULIN LISPRO (334)
CLOZAPINE (198)
RISPERIDONE (176)
OXAZEPAM (152)
BISOPROLOL (150)
LEVETIRACETAM (126)
ACETAMINOPHEN (123)
METFORMIN (116)
INSULIN GLARGINE (114)
CLONAZEPAM (112)
Which DULOXETINE Alternatives Have Lower Wrong patient received product Risk?
DULOXETINE vs DUPILUMAB
DULOXETINE vs DURAGESIC
DULOXETINE vs DUROGESIC
DULOXETINE vs DUROTEP MT
DULOXETINE vs DURVALUMAB