Does DULOXETINE Cause Extra dose administered? 43 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 43 reports of Extra dose administered have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 0.1% of all adverse event reports for DULOXETINE.
43
Reports of Extra dose administered with DULOXETINE
0.1%
of all DULOXETINE reports
2
Deaths
5
Hospitalizations
How Dangerous Is Extra dose administered From DULOXETINE?
Of the 43 reports, 2 (4.7%) resulted in death, 5 (11.6%) required hospitalization, and 1 (2.3%) were considered life-threatening.
Is Extra dose administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 43 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 Extra dose administered?
TIRZEPATIDE (6,774)
DULAGLUTIDE (3,047)
LORATADINE (1,556)
DUPILUMAB (1,422)
FEXOFENADINE (1,413)
NAPROXEN (908)
POLYETHYLENE GLYCOL 3350 (589)
ACETAMINOPHEN (552)
DALFAMPRIDINE (519)
FLUTICASONE\SALMETEROL (499)
Which DULOXETINE Alternatives Have Lower Extra dose administered Risk?
DULOXETINE vs DUPILUMAB
DULOXETINE vs DURAGESIC
DULOXETINE vs DUROGESIC
DULOXETINE vs DUROTEP MT
DULOXETINE vs DURVALUMAB