Does GUSELKUMAB Cause Liquid product physical issue? 194 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 194 reports of Liquid product physical issue have been filed in association with GUSELKUMAB (TREMFYA). This represents 0.7% of all adverse event reports for GUSELKUMAB.
194
Reports of Liquid product physical issue with GUSELKUMAB
0.7%
of all GUSELKUMAB reports
0
Deaths
1
Hospitalizations
How Dangerous Is Liquid product physical issue From GUSELKUMAB?
Of the 194 reports, 1 (0.5%) required hospitalization.
Is Liquid product physical issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GUSELKUMAB. However, 194 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 Liquid product physical issue?
SOMATROPIN (679)
EPINEPHRINE (618)
ADALIMUMAB (404)
USTEKINUMAB (226)
INSULIN ASPART (211)
TESTOSTERONE CYPIONATE (195)
HUMAN IMMUNOGLOBULIN G (142)
ERENUMAB-AOOE (95)
BUDESONIDE (92)
CYCLOSPORINE (86)
Which GUSELKUMAB Alternatives Have Lower Liquid product physical issue Risk?
GUSELKUMAB vs HAIR KERATIN AMINO ACIDS GOLD COMPLEX
GUSELKUMAB vs HALDOL
GUSELKUMAB vs HALOBETASOL
GUSELKUMAB vs HALOPERIDOL
GUSELKUMAB vs HALOPERIDOL DECANOATE