Does DULOXETINE Cause Product quality issue? 114 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 114 reports of Product quality issue have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 0.2% of all adverse event reports for DULOXETINE.
114
Reports of Product quality issue with DULOXETINE
0.2%
of all DULOXETINE reports
1
Deaths
6
Hospitalizations
How Dangerous Is Product quality issue From DULOXETINE?
Of the 114 reports, 1 (0.9%) resulted in death, 6 (5.3%) required hospitalization, and 5 (4.4%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 114 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which DULOXETINE Alternatives Have Lower Product quality issue Risk?
DULOXETINE vs DUPILUMAB
DULOXETINE vs DURAGESIC
DULOXETINE vs DUROGESIC
DULOXETINE vs DUROTEP MT
DULOXETINE vs DURVALUMAB