Does GUSELKUMAB Cause Drug delivery system malfunction? 686 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 686 reports of Drug delivery system malfunction have been filed in association with GUSELKUMAB (TREMFYA). This represents 2.5% of all adverse event reports for GUSELKUMAB.
686
Reports of Drug delivery system malfunction with GUSELKUMAB
2.5%
of all GUSELKUMAB reports
0
Deaths
9
Hospitalizations
How Dangerous Is Drug delivery system malfunction From GUSELKUMAB?
Of the 686 reports, 9 (1.3%) required hospitalization.
Is Drug delivery system malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GUSELKUMAB. However, 686 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 Drug delivery system malfunction?
GOLIMUMAB (406)
PEGINTERFERON BETA-1A (367)
TOCILIZUMAB (263)
EXENATIDE (243)
USTEKINUMAB (194)
PEGFILGRASTIM (187)
INTERFERON BETA-1A (185)
ALBUTEROL (142)
BUDESONIDE\FORMOTEROL (115)
SOMATROPIN (63)
Which GUSELKUMAB Alternatives Have Lower Drug delivery system malfunction Risk?
GUSELKUMAB vs HAIR KERATIN AMINO ACIDS GOLD COMPLEX
GUSELKUMAB vs HALDOL
GUSELKUMAB vs HALOBETASOL
GUSELKUMAB vs HALOPERIDOL
GUSELKUMAB vs HALOPERIDOL DECANOATE