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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 dose omission? 1,911 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 1,911 reports of Drug dose omission have been filed in association with USTEKINUMAB (PYZCHIVA). This represents 2.2% of all adverse event reports for USTEKINUMAB.

1,911
Reports of Drug dose omission with USTEKINUMAB
2.2%
of all USTEKINUMAB reports
3
Deaths
64
Hospitalizations

How Dangerous Is Drug dose omission From USTEKINUMAB?

Of the 1,911 reports, 3 (0.2%) resulted in death, 64 (3.3%) required hospitalization.

Is Drug dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for USTEKINUMAB. However, 1,911 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 dose omission?

ETANERCEPT (10,871) CINACALCET (8,683) EVOLOCUMAB (4,914) ADALIMUMAB (3,993) INSULIN LISPRO (3,063) GOLIMUMAB (2,652) TERIPARATIDE (2,616) APREMILAST (2,466) ALBUTEROL (2,309) FLUTICASONE\SALMETEROL (2,153)

Which USTEKINUMAB Alternatives Have Lower Drug dose omission 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 dose omission Reports All Drugs Causing Drug dose omission USTEKINUMAB Demographics