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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 Drug level decreased? 340 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 340 reports of Drug level decreased have been filed in association with USTEKINUMAB (PYZCHIVA). This represents 0.4% of all adverse event reports for USTEKINUMAB.

340
Reports of Drug level decreased with USTEKINUMAB
0.4%
of all USTEKINUMAB reports
3
Deaths
44
Hospitalizations

How Dangerous Is Drug level decreased From USTEKINUMAB?

Of the 340 reports, 3 (0.9%) resulted in death, 44 (12.9%) required hospitalization.

Is Drug level decreased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for USTEKINUMAB. However, 340 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 Drug level decreased?

INFLIXIMAB (1,401) INFLIXIMAB-DYYB (1,207) ADALIMUMAB (1,186) VEDOLIZUMAB (937) TACROLIMUS (274) EVEROLIMUS (161) VORICONAZOLE (146) LEVETIRACETAM (144) LAMOTRIGINE (142) PHENYTOIN (135)

Which USTEKINUMAB Alternatives Have Lower Drug level decreased Risk?

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

Related Pages

USTEKINUMAB Full Profile All Drug level decreased Reports All Drugs Causing Drug level decreased USTEKINUMAB Demographics