Does USTEKINUMAB Cause Product storage error? 1,338 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,338 reports of Product storage error have been filed in association with USTEKINUMAB (PYZCHIVA). This represents 1.6% of all adverse event reports for USTEKINUMAB.
1,338
Reports of Product storage error with USTEKINUMAB
1.6%
of all USTEKINUMAB reports
0
Deaths
43
Hospitalizations
How Dangerous Is Product storage error From USTEKINUMAB?
Of the 1,338 reports, 43 (3.2%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for USTEKINUMAB. However, 1,338 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 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 USTEKINUMAB Alternatives Have Lower Product storage error Risk?
USTEKINUMAB vs USTEKINUMAB-STBA
USTEKINUMAB vs VADADUSTAT
USTEKINUMAB vs VALACYCLOVIR
USTEKINUMAB vs VALBENAZINE
USTEKINUMAB vs VALBENAZINE DITOSYLATE