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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does GUSELKUMAB Cause Product packaging issue? 76 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 76 reports of Product packaging issue have been filed in association with GUSELKUMAB (TREMFYA). This represents 0.3% of all adverse event reports for GUSELKUMAB.

76
Reports of Product packaging issue with GUSELKUMAB
0.3%
of all GUSELKUMAB reports
0
Deaths
1
Hospitalizations

How Dangerous Is Product packaging issue From GUSELKUMAB?

Of the 76 reports, 1 (1.3%) required hospitalization.

Is Product packaging issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GUSELKUMAB. However, 76 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 Product packaging issue?

ACETAMINOPHEN (448) LOPERAMIDE (351) DIMETHICONE\LOPERAMIDE (348) USTEKINUMAB (221) FENTANYL (200) MINOXIDIL (173) CETIRIZINE (166) ESTRADIOL (163) GOLIMUMAB (95) CYCLOSPORINE (93)

Which GUSELKUMAB Alternatives Have Lower Product packaging issue Risk?

GUSELKUMAB vs HAIR KERATIN AMINO ACIDS GOLD COMPLEX GUSELKUMAB vs HALDOL GUSELKUMAB vs HALOBETASOL GUSELKUMAB vs HALOPERIDOL GUSELKUMAB vs HALOPERIDOL DECANOATE

Related Pages

GUSELKUMAB Full Profile All Product packaging issue Reports All Drugs Causing Product packaging issue GUSELKUMAB Demographics