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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 Decreased activity? 106 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 106 reports of Decreased activity have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 0.2% of all adverse event reports for DULOXETINE.

106
Reports of Decreased activity with DULOXETINE
0.2%
of all DULOXETINE reports
0
Deaths
20
Hospitalizations

How Dangerous Is Decreased activity From DULOXETINE?

Of the 106 reports, 20 (18.9%) required hospitalization, and 6 (5.7%) were considered life-threatening.

Is Decreased activity Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DULOXETINE. However, 106 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 Decreased activity?

NIRAPARIB (586) SACUBITRIL\VALSARTAN (570) RUXOLITINIB (558) DUPILUMAB (231) LEVOTHYROXINE (201) TREPROSTINIL (195) PREDNISONE (193) ALBUTEROL (190) EMTRICITABINE\TENOFOVIR DISOPROXIL (186) TERIPARATIDE (156)

Which DULOXETINE Alternatives Have Lower Decreased activity Risk?

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

Related Pages

DULOXETINE Full Profile All Decreased activity Reports All Drugs Causing Decreased activity DULOXETINE Demographics