Does GUSELKUMAB Cause Product storage error? 1,017 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,017 reports of Product storage error have been filed in association with GUSELKUMAB (TREMFYA). This represents 3.6% of all adverse event reports for GUSELKUMAB.
1,017
Reports of Product storage error with GUSELKUMAB
3.6%
of all GUSELKUMAB reports
1
Deaths
11
Hospitalizations
How Dangerous Is Product storage error From GUSELKUMAB?
Of the 1,017 reports, 1 (0.1%) resulted in death, 11 (1.1%) required hospitalization.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GUSELKUMAB. However, 1,017 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)
Inappropriate schedule of product administration (830)
Device deployment issue (778)
What Other Drugs Cause Product storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which GUSELKUMAB Alternatives Have Lower Product storage error Risk?
GUSELKUMAB vs HAIR KERATIN AMINO ACIDS GOLD COMPLEX
GUSELKUMAB vs HALDOL
GUSELKUMAB vs HALOBETASOL
GUSELKUMAB vs HALOPERIDOL
GUSELKUMAB vs HALOPERIDOL DECANOATE