Does DULOXETINE Cause Product communication issue? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Product communication issue have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 0.0% of all adverse event reports for DULOXETINE.
12
Reports of Product communication issue with DULOXETINE
0.0%
of all DULOXETINE reports
1
Deaths
1
Hospitalizations
How Dangerous Is Product communication issue From DULOXETINE?
Of the 12 reports, 1 (8.3%) resulted in death, 1 (8.3%) required hospitalization, and 1 (8.3%) were considered life-threatening.
Is Product communication issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 12 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 communication issue?
EVOLOCUMAB (2,341)
SEMAGLUTIDE (842)
ERENUMAB-AOOE (598)
SOMATROPIN (350)
PEGFILGRASTIM (333)
ETANERCEPT (122)
ALBUTEROL (121)
NIRMATRELVIR\RITONAVIR (70)
DENOSUMAB (68)
LEVODOPA (61)
Which DULOXETINE Alternatives Have Lower Product communication issue Risk?
DULOXETINE vs DUPILUMAB
DULOXETINE vs DURAGESIC
DULOXETINE vs DUROGESIC
DULOXETINE vs DUROTEP MT
DULOXETINE vs DURVALUMAB