Does DULOXETINE Cause Presyncope? 110 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 110 reports of Presyncope have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 0.2% of all adverse event reports for DULOXETINE.
110
Reports of Presyncope with DULOXETINE
0.2%
of all DULOXETINE reports
0
Deaths
23
Hospitalizations
How Dangerous Is Presyncope From DULOXETINE?
Of the 110 reports, 23 (20.9%) required hospitalization, and 5 (4.5%) were considered life-threatening.
Is Presyncope Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 110 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 Presyncope?
TREPROSTINIL (585)
BISOPROLOL (485)
LEVONORGESTREL (429)
ADALIMUMAB (420)
AMBRISENTAN (407)
ASPIRIN (370)
TAMSULOSIN (361)
FUROSEMIDE (348)
SERTRALINE (337)
ETANERCEPT (334)
Which DULOXETINE Alternatives Have Lower Presyncope Risk?
DULOXETINE vs DUPILUMAB
DULOXETINE vs DURAGESIC
DULOXETINE vs DUROGESIC
DULOXETINE vs DUROTEP MT
DULOXETINE vs DURVALUMAB