Does GUSELKUMAB Cause Product label issue? 177 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 177 reports of Product label issue have been filed in association with GUSELKUMAB (TREMFYA). This represents 0.6% of all adverse event reports for GUSELKUMAB.
177
Reports of Product label issue with GUSELKUMAB
0.6%
of all GUSELKUMAB reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product label issue From GUSELKUMAB?
Of the 177 reports, 3 (1.7%) required hospitalization.
Is Product label issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GUSELKUMAB. However, 177 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 label issue?
RIVAROXABAN (379)
ACETAMINOPHEN (276)
USTEKINUMAB (164)
DIMETHICONE\LOPERAMIDE (154)
CETIRIZINE (138)
IBUPROFEN (99)
GOLIMUMAB (76)
POLYETHYLENE GLYCOL 3350 (76)
FENTANYL (72)
LOPERAMIDE (72)
Which GUSELKUMAB Alternatives Have Lower Product label issue Risk?
GUSELKUMAB vs HAIR KERATIN AMINO ACIDS GOLD COMPLEX
GUSELKUMAB vs HALDOL
GUSELKUMAB vs HALOBETASOL
GUSELKUMAB vs HALOPERIDOL
GUSELKUMAB vs HALOPERIDOL DECANOATE