Does USTEKINUMAB Cause Device malfunction? 610 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 610 reports of Device malfunction have been filed in association with USTEKINUMAB (PYZCHIVA). This represents 0.7% of all adverse event reports for USTEKINUMAB.
610
Reports of Device malfunction with USTEKINUMAB
0.7%
of all USTEKINUMAB reports
0
Deaths
11
Hospitalizations
How Dangerous Is Device malfunction From USTEKINUMAB?
Of the 610 reports, 11 (1.8%) required hospitalization, and 1 (0.2%) were considered life-threatening.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for USTEKINUMAB. However, 610 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 malfunction?
PEGFILGRASTIM (6,818)
EXENATIDE (3,273)
BUDESONIDE\FORMOTEROL (2,771)
ABATACEPT (2,459)
SOMATROPIN (2,311)
GOLIMUMAB (2,293)
SECUKINUMAB (2,259)
ALBUTEROL (2,257)
GUSELKUMAB (1,410)
MOMETASONE FUROATE (1,332)
Which USTEKINUMAB Alternatives Have Lower Device malfunction Risk?
USTEKINUMAB vs USTEKINUMAB-STBA
USTEKINUMAB vs VADADUSTAT
USTEKINUMAB vs VALACYCLOVIR
USTEKINUMAB vs VALBENAZINE
USTEKINUMAB vs VALBENAZINE DITOSYLATE