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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 Hypersensitivity? 575 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 575 reports of Hypersensitivity have been filed in association with DULOXETINE (Duloxetine Hydrochloride). This represents 1.1% of all adverse event reports for DULOXETINE.

575
Reports of Hypersensitivity with DULOXETINE
1.1%
of all DULOXETINE reports
0
Deaths
82
Hospitalizations

How Dangerous Is Hypersensitivity From DULOXETINE?

Of the 575 reports, 82 (14.3%) required hospitalization, and 10 (1.7%) were considered life-threatening.

Is Hypersensitivity Listed in the Official Label?

Yes, Hypersensitivity is listed as a known adverse reaction in the official FDA drug label for DULOXETINE.

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 Hypersensitivity?

ETANERCEPT (10,846) ADALIMUMAB (10,641) METHOTREXATE (9,799) TOCILIZUMAB (9,076) ABATACEPT (8,945) INFLIXIMAB (8,519) RITUXIMAB (8,408) ADAPALENE (8,356) LEFLUNOMIDE (7,926) CERTOLIZUMAB PEGOL (7,353)

Which DULOXETINE Alternatives Have Lower Hypersensitivity Risk?

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

Related Pages

DULOXETINE Full Profile All Hypersensitivity Reports All Drugs Causing Hypersensitivity DULOXETINE Demographics