Does DULOXETINE Cause Affect lability? 2,510 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,510 reports of Affect lability have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 4.8% of all adverse event reports for DULOXETINE.
2,510
Reports of Affect lability with DULOXETINE
4.8%
of all DULOXETINE reports
15
Deaths
237
Hospitalizations
How Dangerous Is Affect lability From DULOXETINE?
Of the 2,510 reports, 15 (0.6%) resulted in death, 237 (9.4%) required hospitalization, and 41 (1.6%) were considered life-threatening.
Is Affect lability Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 2,510 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 Affect lability?
METFORMIN (291)
AMLODIPINE (274)
METHOTREXATE (266)
ATORVASTATIN (259)
IRBESARTAN (257)
LEVOTHYROXINE (251)
SITAGLIPTIN (244)
ESOMEPRAZOLE (234)
ASPIRIN (224)
PREDNISONE (196)
Which DULOXETINE Alternatives Have Lower Affect lability Risk?
DULOXETINE vs DUPILUMAB
DULOXETINE vs DURAGESIC
DULOXETINE vs DUROGESIC
DULOXETINE vs DUROTEP MT
DULOXETINE vs DURVALUMAB