Does GUSELKUMAB Cause Hypersensitivity? 185 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 185 reports of Hypersensitivity have been filed in association with GUSELKUMAB (TREMFYA). This represents 0.7% of all adverse event reports for GUSELKUMAB.
185
Reports of Hypersensitivity with GUSELKUMAB
0.7%
of all GUSELKUMAB reports
0
Deaths
16
Hospitalizations
How Dangerous Is Hypersensitivity From GUSELKUMAB?
Of the 185 reports, 16 (8.6%) required hospitalization, and 6 (3.2%) 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 GUSELKUMAB.
What Other Side Effects Does GUSELKUMAB Cause?
Product dose omission issue (9,267)
Accidental exposure to product (2,941)
Drug ineffective (1,971)
Needle issue (1,933)
Psoriasis (1,817)
Device issue (1,613)
Device malfunction (1,410)
Off label use (1,186)
Product storage error (1,017)
Inappropriate schedule of product administration (830)
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 GUSELKUMAB Alternatives Have Lower Hypersensitivity Risk?
GUSELKUMAB vs HAIR KERATIN AMINO ACIDS GOLD COMPLEX
GUSELKUMAB vs HALDOL
GUSELKUMAB vs HALOBETASOL
GUSELKUMAB vs HALOPERIDOL
GUSELKUMAB vs HALOPERIDOL DECANOATE