Does GUSELKUMAB Cause Device leakage? 712 Reports in FDA Database
Visibly Younger Skin in Weeks
Synevra Lift & Lock — Swiss peptide serum + nutrients. 60-day money-back guarantee.
According to the FDA Adverse Event Reporting System (FAERS), 712 reports of Device leakage have been filed in association with GUSELKUMAB (TREMFYA). This represents 2.5% of all adverse event reports for GUSELKUMAB.
712
Reports of Device leakage with GUSELKUMAB
2.5%
of all GUSELKUMAB reports
0
Deaths
2
Hospitalizations
How Dangerous Is Device leakage From GUSELKUMAB?
Of the 712 reports, 2 (0.3%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Device leakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GUSELKUMAB. However, 712 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 Device leakage?
SOMATROPIN (9,113)
LEUPROLIDE (5,861)
EXENATIDE (5,115)
PEGFILGRASTIM (1,380)
ALBIGLUTIDE (1,195)
SECUKINUMAB (910)
RISPERIDONE (878)
TREPROSTINIL (874)
DEVICE (795)
ABATACEPT (671)
Which GUSELKUMAB Alternatives Have Lower Device leakage Risk?
GUSELKUMAB vs HAIR KERATIN AMINO ACIDS GOLD COMPLEX
GUSELKUMAB vs HALDOL
GUSELKUMAB vs HALOBETASOL
GUSELKUMAB vs HALOPERIDOL
GUSELKUMAB vs HALOPERIDOL DECANOATE