Does DULOXETINE Cause Product odour abnormal? 25 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 25 reports of Product odour abnormal have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 0.1% of all adverse event reports for DULOXETINE.
25
Reports of Product odour abnormal with DULOXETINE
0.1%
of all DULOXETINE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product odour abnormal From DULOXETINE?
Of the 25 reports, 1 (4.0%) required hospitalization, and 1 (4.0%) were considered life-threatening.
Is Product odour abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 25 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 odour abnormal?
ICOSAPENT ETHYL (911)
BUPROPION (491)
FLUTICASONE (482)
POLYETHYLENE GLYCOL 3350 (381)
METFORMIN (323)
OMEGA-3-ACID ETHYL ESTERS (194)
IBUPROFEN (184)
LEVOTHYROXINE (155)
TESTOSTERONE (145)
PROGESTERONE (134)
Which DULOXETINE Alternatives Have Lower Product odour abnormal Risk?
DULOXETINE vs DUPILUMAB
DULOXETINE vs DURAGESIC
DULOXETINE vs DUROGESIC
DULOXETINE vs DUROTEP MT
DULOXETINE vs DURVALUMAB