Does GUSELKUMAB Cause Product leakage? 661 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 661 reports of Product leakage have been filed in association with GUSELKUMAB (TREMFYA). This represents 2.4% of all adverse event reports for GUSELKUMAB.
661
Reports of Product leakage with GUSELKUMAB
2.4%
of all GUSELKUMAB reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product leakage From GUSELKUMAB?
Of the 661 reports, 2 (0.3%) required hospitalization.
Is Product leakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GUSELKUMAB. However, 661 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 leakage?
INSULIN ASPART (361)
USTEKINUMAB (344)
LEUPROLIDE (331)
SUMATRIPTAN (275)
TREPROSTINIL (213)
ABATACEPT (124)
SECUKINUMAB (116)
PALIPERIDONE (92)
ICOSAPENT ETHYL (80)
GOLIMUMAB (79)
Which GUSELKUMAB Alternatives Have Lower Product leakage Risk?
GUSELKUMAB vs HAIR KERATIN AMINO ACIDS GOLD COMPLEX
GUSELKUMAB vs HALDOL
GUSELKUMAB vs HALOBETASOL
GUSELKUMAB vs HALOPERIDOL
GUSELKUMAB vs HALOPERIDOL DECANOATE