Does GUSELKUMAB Cause Incorrect dose administered? 199 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 199 reports of Incorrect dose administered have been filed in association with GUSELKUMAB (TREMFYA). This represents 0.7% of all adverse event reports for GUSELKUMAB.
199
Reports of Incorrect dose administered with GUSELKUMAB
0.7%
of all GUSELKUMAB reports
0
Deaths
2
Hospitalizations
How Dangerous Is Incorrect dose administered From GUSELKUMAB?
Of the 199 reports, 2 (1.0%) required hospitalization.
Is Incorrect dose administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GUSELKUMAB. However, 199 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 Incorrect dose administered?
TIRZEPATIDE (23,301)
ADALIMUMAB (14,000)
DUPILUMAB (9,907)
RANITIDINE (9,337)
INSULIN LISPRO (8,318)
ACETAMINOPHEN (5,316)
DULAGLUTIDE (5,207)
SECUKINUMAB (4,524)
INSULIN GLARGINE (3,070)
SOMATROPIN (2,772)
Which GUSELKUMAB Alternatives Have Lower Incorrect dose administered Risk?
GUSELKUMAB vs HAIR KERATIN AMINO ACIDS GOLD COMPLEX
GUSELKUMAB vs HALDOL
GUSELKUMAB vs HALOBETASOL
GUSELKUMAB vs HALOPERIDOL
GUSELKUMAB vs HALOPERIDOL DECANOATE