Does DULOXETINE Cause Adverse event? 344 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 344 reports of Adverse event have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 0.7% of all adverse event reports for DULOXETINE.
344
Reports of Adverse event with DULOXETINE
0.7%
of all DULOXETINE reports
5
Deaths
35
Hospitalizations
How Dangerous Is Adverse event From DULOXETINE?
Of the 344 reports, 5 (1.5%) resulted in death, 35 (10.2%) required hospitalization.
Is Adverse event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 344 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 Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which DULOXETINE Alternatives Have Lower Adverse event Risk?
DULOXETINE vs DUPILUMAB
DULOXETINE vs DURAGESIC
DULOXETINE vs DUROGESIC
DULOXETINE vs DUROTEP MT
DULOXETINE vs DURVALUMAB