Does DULOXETINE Cause Product use complaint? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Product use complaint have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 0.0% of all adverse event reports for DULOXETINE.
13
Reports of Product use complaint with DULOXETINE
0.0%
of all DULOXETINE reports
1
Deaths
1
Hospitalizations
How Dangerous Is Product use complaint From DULOXETINE?
Of the 13 reports, 1 (7.7%) resulted in death, 1 (7.7%) required hospitalization.
Is Product use complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 13 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 complaint?
TROFINETIDE (472)
ENZALUTAMIDE (336)
LIFITEGRAST (326)
VOXELOTOR (298)
CLASCOTERONE (285)
NIRMATRELVIR\RITONAVIR (248)
ABALOPARATIDE (224)
ESTRADIOL (208)
MOLNUPIRAVIR (206)
ACETAMINOPHEN (202)
Which DULOXETINE Alternatives Have Lower Product use complaint Risk?
DULOXETINE vs DUPILUMAB
DULOXETINE vs DURAGESIC
DULOXETINE vs DUROGESIC
DULOXETINE vs DUROTEP MT
DULOXETINE vs DURVALUMAB