Does DULOXETINE Cause Withdrawal syndrome? 1,328 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,328 reports of Withdrawal syndrome have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 2.5% of all adverse event reports for DULOXETINE.
1,328
Reports of Withdrawal syndrome with DULOXETINE
2.5%
of all DULOXETINE reports
19
Deaths
191
Hospitalizations
How Dangerous Is Withdrawal syndrome From DULOXETINE?
Of the 1,328 reports, 19 (1.4%) resulted in death, 191 (14.4%) required hospitalization, and 102 (7.7%) were considered life-threatening.
Is Withdrawal syndrome Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 1,328 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 Withdrawal syndrome?
ACETAMINOPHEN\OXYCODONE (4,046)
PREGABALIN (3,329)
OXYCODONE (2,798)
ACETAMINOPHEN\HYDROCODONE (2,636)
FENTANYL (1,948)
MORPHINE (1,674)
TRAMADOL (1,582)
VENLAFAXINE (1,516)
BUPRENORPHINE (1,266)
HYDROMORPHONE (1,040)
Which DULOXETINE Alternatives Have Lower Withdrawal syndrome Risk?
DULOXETINE vs DUPILUMAB
DULOXETINE vs DURAGESIC
DULOXETINE vs DUROGESIC
DULOXETINE vs DUROTEP MT
DULOXETINE vs DURVALUMAB