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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 UPADACITINIB Cause Post procedural infection? 188 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 188 reports of Post procedural infection have been filed in association with UPADACITINIB (Rinvoq). This represents 0.3% of all adverse event reports for UPADACITINIB.

188
Reports of Post procedural infection with UPADACITINIB
0.3%
of all UPADACITINIB reports
2
Deaths
57
Hospitalizations

How Dangerous Is Post procedural infection From UPADACITINIB?

Of the 188 reports, 2 (1.1%) resulted in death, 57 (30.3%) required hospitalization, and 1 (0.5%) were considered life-threatening.

Is Post procedural infection Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for UPADACITINIB. However, 188 reports have been filed with the FAERS database.

What Other Side Effects Does UPADACITINIB Cause?

Pain (4,444) Arthralgia (3,815) Drug ineffective (3,384) Covid-19 (2,978) Rheumatoid arthritis (2,730) Pain in extremity (2,353) Fatigue (2,153) Fall (2,081) Surgery (2,037) Therapy interrupted (1,741)

What Other Drugs Cause Post procedural infection?

ADALIMUMAB (1,109) ETANERCEPT (362) METHOTREXATE (226) INFLIXIMAB (223) TOFACITINIB (184) GOLIMUMAB (177) VEDOLIZUMAB (166) RISANKIZUMAB-RZAA (157) USTEKINUMAB (150) ABATACEPT (136)

Which UPADACITINIB Alternatives Have Lower Post procedural infection Risk?

UPADACITINIB vs URAPIDIL UPADACITINIB vs UREA UPADACITINIB vs URIDINE TRIACETATE UPADACITINIB vs UROFOLLITROPIN UPADACITINIB vs URSODIOL

Related Pages

UPADACITINIB Full Profile All Post procedural infection Reports All Drugs Causing Post procedural infection UPADACITINIB Demographics