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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 Drug dose omission? 539 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 539 reports of Drug dose omission have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 1.0% of all adverse event reports for DULOXETINE.

539
Reports of Drug dose omission with DULOXETINE
1.0%
of all DULOXETINE reports
0
Deaths
41
Hospitalizations

How Dangerous Is Drug dose omission From DULOXETINE?

Of the 539 reports, 41 (7.6%) required hospitalization, and 3 (0.6%) were considered life-threatening.

Is Drug dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 539 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 Drug dose omission?

ETANERCEPT (10,871) CINACALCET (8,683) EVOLOCUMAB (4,914) ADALIMUMAB (3,993) INSULIN LISPRO (3,063) GOLIMUMAB (2,652) TERIPARATIDE (2,616) APREMILAST (2,466) ALBUTEROL (2,309) FLUTICASONE\SALMETEROL (2,153)

Which DULOXETINE Alternatives Have Lower Drug dose omission Risk?

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

Related Pages

DULOXETINE Full Profile All Drug dose omission Reports All Drugs Causing Drug dose omission DULOXETINE Demographics