Does USTEKINUMAB Cause Device issue? 1,716 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,716 reports of Device issue have been filed in association with USTEKINUMAB (PYZCHIVA). This represents 2.0% of all adverse event reports for USTEKINUMAB.
1,716
Reports of Device issue with USTEKINUMAB
2.0%
of all USTEKINUMAB reports
0
Deaths
24
Hospitalizations
How Dangerous Is Device issue From USTEKINUMAB?
Of the 1,716 reports, 24 (1.4%) required hospitalization, and 2 (0.1%) were considered life-threatening.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for USTEKINUMAB. However, 1,716 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 Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
EVOLOCUMAB (1,659)
Which USTEKINUMAB Alternatives Have Lower Device issue Risk?
USTEKINUMAB vs USTEKINUMAB-STBA
USTEKINUMAB vs VADADUSTAT
USTEKINUMAB vs VALACYCLOVIR
USTEKINUMAB vs VALBENAZINE
USTEKINUMAB vs VALBENAZINE DITOSYLATE