Does GUSELKUMAB Cause Product use issue? 262 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 262 reports of Product use issue have been filed in association with GUSELKUMAB (TREMFYA). This represents 0.9% of all adverse event reports for GUSELKUMAB.
262
Reports of Product use issue with GUSELKUMAB
0.9%
of all GUSELKUMAB reports
1
Deaths
22
Hospitalizations
How Dangerous Is Product use issue From GUSELKUMAB?
Of the 262 reports, 1 (0.4%) resulted in death, 22 (8.4%) required hospitalization, and 3 (1.1%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GUSELKUMAB. However, 262 reports have been filed with the FAERS database.
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 Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which GUSELKUMAB Alternatives Have Lower Product use issue Risk?
GUSELKUMAB vs HAIR KERATIN AMINO ACIDS GOLD COMPLEX
GUSELKUMAB vs HALDOL
GUSELKUMAB vs HALOBETASOL
GUSELKUMAB vs HALOPERIDOL
GUSELKUMAB vs HALOPERIDOL DECANOATE