Does USTEKINUMAB Cause Incorrect product storage? 299 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 299 reports of Incorrect product storage have been filed in association with USTEKINUMAB (PYZCHIVA). This represents 0.4% of all adverse event reports for USTEKINUMAB.
299
Reports of Incorrect product storage with USTEKINUMAB
0.4%
of all USTEKINUMAB reports
0
Deaths
4
Hospitalizations
How Dangerous Is Incorrect product storage From USTEKINUMAB?
Of the 299 reports, 4 (1.3%) required hospitalization.
Is Incorrect product storage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for USTEKINUMAB. However, 299 reports have been filed with the FAERS database.
What Other Side Effects Does USTEKINUMAB Cause?
Drug ineffective (12,471)
Off label use (10,990)
Product dose omission issue (9,405)
Fatigue (5,457)
Product use issue (5,008)
Psoriasis (4,955)
Pain (4,872)
Rash (4,736)
Crohn's disease (4,662)
Arthralgia (4,608)
What Other Drugs Cause Incorrect product storage?
ETANERCEPT (2,149)
INSULIN LISPRO (1,114)
ABATACEPT (583)
TERIPARATIDE (573)
ADALIMUMAB (476)
GOLIMUMAB (392)
INSULIN GLARGINE (341)
INSULIN HUMAN (336)
ERYTHROPOIETIN (268)
CYCLOSPORINE (203)
Which USTEKINUMAB Alternatives Have Lower Incorrect product storage Risk?
USTEKINUMAB vs USTEKINUMAB-STBA
USTEKINUMAB vs VADADUSTAT
USTEKINUMAB vs VALACYCLOVIR
USTEKINUMAB vs VALBENAZINE
USTEKINUMAB vs VALBENAZINE DITOSYLATE