Does DULOXETINE Cause Product administration error? 64 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 64 reports of Product administration error have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 0.1% of all adverse event reports for DULOXETINE.
64
Reports of Product administration error with DULOXETINE
0.1%
of all DULOXETINE reports
10
Deaths
33
Hospitalizations
How Dangerous Is Product administration error From DULOXETINE?
Of the 64 reports, 10 (15.6%) resulted in death, 33 (51.6%) required hospitalization, and 5 (7.8%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 64 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 administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which DULOXETINE Alternatives Have Lower Product administration error Risk?
DULOXETINE vs DUPILUMAB
DULOXETINE vs DURAGESIC
DULOXETINE vs DUROGESIC
DULOXETINE vs DUROTEP MT
DULOXETINE vs DURVALUMAB