Does DULOXETINE Cause Condition aggravated? 663 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 663 reports of Condition aggravated have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 1.3% of all adverse event reports for DULOXETINE.
663
Reports of Condition aggravated with DULOXETINE
1.3%
of all DULOXETINE reports
14
Deaths
249
Hospitalizations
How Dangerous Is Condition aggravated From DULOXETINE?
Of the 663 reports, 14 (2.1%) resulted in death, 249 (37.6%) required hospitalization, and 32 (4.8%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 663 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which DULOXETINE Alternatives Have Lower Condition aggravated Risk?
DULOXETINE vs DUPILUMAB
DULOXETINE vs DURAGESIC
DULOXETINE vs DUROGESIC
DULOXETINE vs DUROTEP MT
DULOXETINE vs DURVALUMAB