Does DULOXETINE Cause Concomitant disease aggravated? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Concomitant disease aggravated have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 0.0% of all adverse event reports for DULOXETINE.
10
Reports of Concomitant disease aggravated with DULOXETINE
0.0%
of all DULOXETINE reports
1
Deaths
2
Hospitalizations
How Dangerous Is Concomitant disease aggravated From DULOXETINE?
Of the 10 reports, 1 (10.0%) resulted in death, 2 (20.0%) required hospitalization.
Is Concomitant disease aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 10 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 Concomitant disease aggravated?
SACUBITRIL\VALSARTAN (533)
SECUKINUMAB (461)
FINGOLIMOD (425)
MACITENTAN (286)
OMALIZUMAB (186)
SELEXIPAG (166)
METHOTREXATE (150)
RUXOLITINIB (142)
OCTREOTIDE (125)
BOSENTAN (123)
Which DULOXETINE Alternatives Have Lower Concomitant disease aggravated Risk?
DULOXETINE vs DUPILUMAB
DULOXETINE vs DURAGESIC
DULOXETINE vs DUROGESIC
DULOXETINE vs DUROTEP MT
DULOXETINE vs DURVALUMAB