Does DULOXETINE Cause Expired product administered? 54 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 54 reports of Expired product administered have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 0.1% of all adverse event reports for DULOXETINE.
54
Reports of Expired product administered with DULOXETINE
0.1%
of all DULOXETINE reports
2
Deaths
3
Hospitalizations
How Dangerous Is Expired product administered From DULOXETINE?
Of the 54 reports, 2 (3.7%) resulted in death, 3 (5.6%) required hospitalization.
Is Expired product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 54 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 Expired product administered?
POLYETHYLENE GLYCOL 3350 (1,637)
NAPROXEN (1,305)
ALBUTEROL (1,233)
LORATADINE (1,095)
MINOXIDIL (982)
ACETAMINOPHEN (797)
INSULIN LISPRO (770)
FLUTICASONE\SALMETEROL (753)
CETIRIZINE (714)
DICLOFENAC (714)
Which DULOXETINE Alternatives Have Lower Expired product administered Risk?
DULOXETINE vs DUPILUMAB
DULOXETINE vs DURAGESIC
DULOXETINE vs DUROGESIC
DULOXETINE vs DUROTEP MT
DULOXETINE vs DURVALUMAB