Does GUSELKUMAB Cause Off label use? 1,186 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,186 reports of Off label use have been filed in association with GUSELKUMAB (TREMFYA). This represents 4.2% of all adverse event reports for GUSELKUMAB.
1,186
Reports of Off label use with GUSELKUMAB
4.2%
of all GUSELKUMAB reports
8
Deaths
90
Hospitalizations
How Dangerous Is Off label use From GUSELKUMAB?
Of the 1,186 reports, 8 (0.7%) resulted in death, 90 (7.6%) required hospitalization, and 9 (0.8%) were considered life-threatening.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GUSELKUMAB. However, 1,186 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)
Product storage error (1,017)
Inappropriate schedule of product administration (830)
Device deployment issue (778)
What Other Drugs Cause Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)
Which GUSELKUMAB Alternatives Have Lower Off label use Risk?
GUSELKUMAB vs HAIR KERATIN AMINO ACIDS GOLD COMPLEX
GUSELKUMAB vs HALDOL
GUSELKUMAB vs HALOBETASOL
GUSELKUMAB vs HALOPERIDOL
GUSELKUMAB vs HALOPERIDOL DECANOATE