Does DULOXETINE Cause Contraindicated product administered? 185 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 185 reports of Contraindicated product administered have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 0.4% of all adverse event reports for DULOXETINE.
185
Reports of Contraindicated product administered with DULOXETINE
0.4%
of all DULOXETINE reports
2
Deaths
32
Hospitalizations
How Dangerous Is Contraindicated product administered From DULOXETINE?
Of the 185 reports, 2 (1.1%) resulted in death, 32 (17.3%) required hospitalization, and 13 (7.0%) were considered life-threatening.
Is Contraindicated product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 185 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 Contraindicated product administered?
ABATACEPT (13,559)
METHOTREXATE (13,121)
ETANERCEPT (12,062)
TOCILIZUMAB (11,547)
ADALIMUMAB (11,270)
LEFLUNOMIDE (11,206)
HYDROXYCHLOROQUINE (10,557)
RITUXIMAB (10,479)
INFLIXIMAB (9,618)
SULFASALAZINE (8,698)
Which DULOXETINE Alternatives Have Lower Contraindicated product administered Risk?
DULOXETINE vs DUPILUMAB
DULOXETINE vs DURAGESIC
DULOXETINE vs DUROGESIC
DULOXETINE vs DUROTEP MT
DULOXETINE vs DURVALUMAB