Does GUSELKUMAB Cause Drug dose omission? 56 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 56 reports of Drug dose omission have been filed in association with GUSELKUMAB (TREMFYA). This represents 0.2% of all adverse event reports for GUSELKUMAB.
56
Reports of Drug dose omission with GUSELKUMAB
0.2%
of all GUSELKUMAB reports
0
Deaths
2
Hospitalizations
How Dangerous Is Drug dose omission From GUSELKUMAB?
Of the 56 reports, 2 (3.6%) required hospitalization.
Is Drug dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GUSELKUMAB. However, 56 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 dose omission?
ETANERCEPT (10,871)
CINACALCET (8,683)
EVOLOCUMAB (4,914)
ADALIMUMAB (3,993)
INSULIN LISPRO (3,063)
GOLIMUMAB (2,652)
TERIPARATIDE (2,616)
APREMILAST (2,466)
ALBUTEROL (2,309)
FLUTICASONE\SALMETEROL (2,153)
Which GUSELKUMAB Alternatives Have Lower Drug dose omission Risk?
GUSELKUMAB vs HAIR KERATIN AMINO ACIDS GOLD COMPLEX
GUSELKUMAB vs HALDOL
GUSELKUMAB vs HALOBETASOL
GUSELKUMAB vs HALOPERIDOL
GUSELKUMAB vs HALOPERIDOL DECANOATE