Does GUSELKUMAB Cause Needle issue? 1,933 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,933 reports of Needle issue have been filed in association with GUSELKUMAB (TREMFYA). This represents 6.9% of all adverse event reports for GUSELKUMAB.
1,933
Reports of Needle issue with GUSELKUMAB
6.9%
of all GUSELKUMAB reports
0
Deaths
9
Hospitalizations
How Dangerous Is Needle issue From GUSELKUMAB?
Of the 1,933 reports, 9 (0.5%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Needle issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GUSELKUMAB. However, 1,933 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)
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)
Device deployment issue (778)
What Other Drugs Cause Needle issue?
OCTREOTIDE (2,740)
USTEKINUMAB (1,930)
EXENATIDE (1,821)
GOLIMUMAB (1,023)
ADALIMUMAB (1,022)
SOMATROPIN (981)
SECUKINUMAB (958)
ABATACEPT (716)
DUPILUMAB (686)
LEUPROLIDE (661)
Which GUSELKUMAB Alternatives Have Lower Needle issue Risk?
GUSELKUMAB vs HAIR KERATIN AMINO ACIDS GOLD COMPLEX
GUSELKUMAB vs HALDOL
GUSELKUMAB vs HALOBETASOL
GUSELKUMAB vs HALOPERIDOL
GUSELKUMAB vs HALOPERIDOL DECANOATE