Does DULOXETINE Cause Product substitution issue? 766 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 766 reports of Product substitution issue have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 1.5% of all adverse event reports for DULOXETINE.
766
Reports of Product substitution issue with DULOXETINE
1.5%
of all DULOXETINE reports
1
Deaths
41
Hospitalizations
How Dangerous Is Product substitution issue From DULOXETINE?
Of the 766 reports, 1 (0.1%) resulted in death, 41 (5.4%) required hospitalization, and 42 (5.5%) were considered life-threatening.
Is Product substitution issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 766 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 substitution issue?
AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (2,832)
BUPROPION (1,578)
METHYLPHENIDATE (1,408)
CLONAZEPAM (1,288)
LAMOTRIGINE (979)
ALBUTEROL (864)
LEVOTHYROXINE (803)
ESTRADIOL (692)
SERTRALINE (636)
LEVETIRACETAM (572)
Which DULOXETINE Alternatives Have Lower Product substitution issue Risk?
DULOXETINE vs DUPILUMAB
DULOXETINE vs DURAGESIC
DULOXETINE vs DUROGESIC
DULOXETINE vs DUROTEP MT
DULOXETINE vs DURVALUMAB