Does DULOXETINE Cause Drug level increased? 98 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 98 reports of Drug level increased have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 0.2% of all adverse event reports for DULOXETINE.
98
Reports of Drug level increased with DULOXETINE
0.2%
of all DULOXETINE reports
11
Deaths
59
Hospitalizations
How Dangerous Is Drug level increased From DULOXETINE?
Of the 98 reports, 11 (11.2%) resulted in death, 59 (60.2%) required hospitalization, and 6 (6.1%) were considered life-threatening.
Is Drug level increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 98 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 Drug level increased?
TACROLIMUS (1,013)
METFORMIN (886)
CLOZAPINE (554)
LAMOTRIGINE (541)
ACETAMINOPHEN (538)
METHOTREXATE (528)
VANCOMYCIN (447)
AMLODIPINE (329)
VORICONAZOLE (325)
OLANZAPINE (283)
Which DULOXETINE Alternatives Have Lower Drug level increased Risk?
DULOXETINE vs DUPILUMAB
DULOXETINE vs DURAGESIC
DULOXETINE vs DUROGESIC
DULOXETINE vs DUROTEP MT
DULOXETINE vs DURVALUMAB