Does DULOXETINE Cause International normalised ratio increased? 51 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 51 reports of International normalised ratio increased have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 0.1% of all adverse event reports for DULOXETINE.
51
Reports of International normalised ratio increased with DULOXETINE
0.1%
of all DULOXETINE reports
1
Deaths
22
Hospitalizations
How Dangerous Is International normalised ratio increased From DULOXETINE?
Of the 51 reports, 1 (2.0%) resulted in death, 22 (43.1%) required hospitalization.
Is International normalised ratio increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 51 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 International normalised ratio increased?
WARFARIN (5,622)
RIVAROXABAN (863)
ACETAMINOPHEN (533)
ASPIRIN (448)
APIXABAN (317)
CLOPIDOGREL BISULFATE (314)
FLUINDIONE (286)
AMIODARONE (277)
FUROSEMIDE (277)
DABIGATRAN ETEXILATE (223)
Which DULOXETINE Alternatives Have Lower International normalised ratio increased Risk?
DULOXETINE vs DUPILUMAB
DULOXETINE vs DURAGESIC
DULOXETINE vs DUROGESIC
DULOXETINE vs DUROTEP MT
DULOXETINE vs DURVALUMAB