Does GUSELKUMAB Cause Wrong technique in product usage process? 307 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 307 reports of Wrong technique in product usage process have been filed in association with GUSELKUMAB (TREMFYA). This represents 1.1% of all adverse event reports for GUSELKUMAB.
307
Reports of Wrong technique in product usage process with GUSELKUMAB
1.1%
of all GUSELKUMAB reports
0
Deaths
1
Hospitalizations
How Dangerous Is Wrong technique in product usage process From GUSELKUMAB?
Of the 307 reports, 1 (0.3%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GUSELKUMAB. However, 307 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which GUSELKUMAB Alternatives Have Lower Wrong technique in product usage process Risk?
GUSELKUMAB vs HAIR KERATIN AMINO ACIDS GOLD COMPLEX
GUSELKUMAB vs HALDOL
GUSELKUMAB vs HALOBETASOL
GUSELKUMAB vs HALOPERIDOL
GUSELKUMAB vs HALOPERIDOL DECANOATE