Does GUSELKUMAB Cause Device issue? 1,613 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,613 reports of Device issue have been filed in association with GUSELKUMAB (TREMFYA). This represents 5.8% of all adverse event reports for GUSELKUMAB.
1,613
Reports of Device issue with GUSELKUMAB
5.8%
of all GUSELKUMAB reports
0
Deaths
7
Hospitalizations
How Dangerous Is Device issue From GUSELKUMAB?
Of the 1,613 reports, 7 (0.4%) required hospitalization.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GUSELKUMAB. However, 1,613 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 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 Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which GUSELKUMAB Alternatives Have Lower Device issue Risk?
GUSELKUMAB vs HAIR KERATIN AMINO ACIDS GOLD COMPLEX
GUSELKUMAB vs HALDOL
GUSELKUMAB vs HALOBETASOL
GUSELKUMAB vs HALOPERIDOL
GUSELKUMAB vs HALOPERIDOL DECANOATE