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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does DULOXETINE Cause Wrong patient? 19 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Wrong patient have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 0.0% of all adverse event reports for DULOXETINE.

19
Reports of Wrong patient with DULOXETINE
0.0%
of all DULOXETINE reports
3
Deaths
19
Hospitalizations

How Dangerous Is Wrong patient From DULOXETINE?

Of the 19 reports, 3 (15.8%) resulted in death, 19 (100.0%) required hospitalization.

Is Wrong patient Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 19 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 patient?

OXAZEPAM (72) CLOZAPINE (70) PREGABALIN (56) RISPERIDONE (51) SERTRALINE (48) PANTOPRAZOLE (45) CYAMEMAZINE (43) FUROSEMIDE (43) LAMOTRIGINE (42) APIXABAN (35)

Which DULOXETINE Alternatives Have Lower Wrong patient Risk?

DULOXETINE vs DUPILUMAB DULOXETINE vs DURAGESIC DULOXETINE vs DUROGESIC DULOXETINE vs DUROTEP MT DULOXETINE vs DURVALUMAB

Related Pages

DULOXETINE Full Profile All Wrong patient Reports All Drugs Causing Wrong patient DULOXETINE Demographics