Does GUSELKUMAB Cause Device defective? 574 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 574 reports of Device defective have been filed in association with GUSELKUMAB (TREMFYA). This represents 2.1% of all adverse event reports for GUSELKUMAB.
574
Reports of Device defective with GUSELKUMAB
2.1%
of all GUSELKUMAB reports
1
Deaths
3
Hospitalizations
How Dangerous Is Device defective From GUSELKUMAB?
Of the 574 reports, 1 (0.2%) resulted in death, 3 (0.5%) required hospitalization.
Is Device defective Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GUSELKUMAB. However, 574 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 defective?
SOMATROPIN (1,719)
USTEKINUMAB (1,071)
SECUKINUMAB (666)
GOLIMUMAB (539)
ABATACEPT (458)
ALBUTEROL (445)
TOCILIZUMAB (400)
INSULIN GLARGINE (397)
EXENATIDE (387)
BUDESONIDE\FORMOTEROL (378)
Which GUSELKUMAB Alternatives Have Lower Device defective Risk?
GUSELKUMAB vs HAIR KERATIN AMINO ACIDS GOLD COMPLEX
GUSELKUMAB vs HALDOL
GUSELKUMAB vs HALOBETASOL
GUSELKUMAB vs HALOPERIDOL
GUSELKUMAB vs HALOPERIDOL DECANOATE