Does DULOXETINE Cause Wrong technique in product usage process? 411 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 411 reports of Wrong technique in product usage process have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 0.8% of all adverse event reports for DULOXETINE.
411
Reports of Wrong technique in product usage process with DULOXETINE
0.8%
of all DULOXETINE reports
4
Deaths
43
Hospitalizations
How Dangerous Is Wrong technique in product usage process From DULOXETINE?
Of the 411 reports, 4 (1.0%) resulted in death, 43 (10.5%) required hospitalization, and 6 (1.5%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 411 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which DULOXETINE Alternatives Have Lower Wrong technique in product usage process Risk?
DULOXETINE vs DUPILUMAB
DULOXETINE vs DURAGESIC
DULOXETINE vs DUROGESIC
DULOXETINE vs DUROTEP MT
DULOXETINE vs DURVALUMAB