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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does USTEKINUMAB Cause Device use error? 64 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 64 reports of Device use error have been filed in association with USTEKINUMAB (PYZCHIVA). This represents 0.1% of all adverse event reports for USTEKINUMAB.

64
Reports of Device use error with USTEKINUMAB
0.1%
of all USTEKINUMAB reports
0
Deaths
2
Hospitalizations

How Dangerous Is Device use error From USTEKINUMAB?

Of the 64 reports, 2 (3.1%) required hospitalization.

Is Device use error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for USTEKINUMAB. However, 64 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 use error?

PEGFILGRASTIM (6,001) ALBUTEROL (5,215) ALBIGLUTIDE (4,056) EVOLOCUMAB (4,002) SOMATROPIN (2,801) FLUTICASONE\SALMETEROL (1,749) FLUTICASONE (783) FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (766) ERENUMAB-AOOE (711) ETANERCEPT (665)

Which USTEKINUMAB Alternatives Have Lower Device use error Risk?

USTEKINUMAB vs USTEKINUMAB-STBA USTEKINUMAB vs VADADUSTAT USTEKINUMAB vs VALACYCLOVIR USTEKINUMAB vs VALBENAZINE USTEKINUMAB vs VALBENAZINE DITOSYLATE

Related Pages

USTEKINUMAB Full Profile All Device use error Reports All Drugs Causing Device use error USTEKINUMAB Demographics