Does GUSELKUMAB Cause Device malfunction? 1,410 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,410 reports of Device malfunction have been filed in association with GUSELKUMAB (TREMFYA). This represents 5.0% of all adverse event reports for GUSELKUMAB.
1,410
Reports of Device malfunction with GUSELKUMAB
5.0%
of all GUSELKUMAB reports
0
Deaths
4
Hospitalizations
How Dangerous Is Device malfunction From GUSELKUMAB?
Of the 1,410 reports, 4 (0.3%) required hospitalization.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GUSELKUMAB. However, 1,410 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)
Off label use (1,186)
Product storage error (1,017)
Inappropriate schedule of product administration (830)
Device deployment issue (778)
What Other Drugs Cause Device malfunction?
PEGFILGRASTIM (6,818)
EXENATIDE (3,273)
BUDESONIDE\FORMOTEROL (2,771)
ABATACEPT (2,459)
SOMATROPIN (2,311)
GOLIMUMAB (2,293)
SECUKINUMAB (2,259)
ALBUTEROL (2,257)
MOMETASONE FUROATE (1,332)
ACLIDINIUM (1,325)
Which GUSELKUMAB Alternatives Have Lower Device malfunction Risk?
GUSELKUMAB vs HAIR KERATIN AMINO ACIDS GOLD COMPLEX
GUSELKUMAB vs HALDOL
GUSELKUMAB vs HALOBETASOL
GUSELKUMAB vs HALOPERIDOL
GUSELKUMAB vs HALOPERIDOL DECANOATE