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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 INFLIXIMAB Cause Post procedural infection? 223 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 223 reports of Post procedural infection have been filed in association with INFLIXIMAB (Renflexis). This represents 0.2% of all adverse event reports for INFLIXIMAB.

223
Reports of Post procedural infection with INFLIXIMAB
0.2%
of all INFLIXIMAB reports
10
Deaths
103
Hospitalizations

How Dangerous Is Post procedural infection From INFLIXIMAB?

Of the 223 reports, 10 (4.5%) resulted in death, 103 (46.2%) required hospitalization, and 2 (0.9%) 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 INFLIXIMAB. However, 223 reports have been filed with the FAERS database.

What Other Side Effects Does INFLIXIMAB Cause?

Off label use (34,801) Drug ineffective (33,738) Condition aggravated (16,616) Rheumatoid arthritis (16,251) Pain (15,061) Fatigue (13,473) Arthralgia (13,441) Infusion related reaction (12,946) Product use issue (12,752) Drug intolerance (11,173)

What Other Drugs Cause Post procedural infection?

ADALIMUMAB (1,109) ETANERCEPT (362) METHOTREXATE (226) UPADACITINIB (188) TOFACITINIB (184) GOLIMUMAB (177) VEDOLIZUMAB (166) RISANKIZUMAB-RZAA (157) USTEKINUMAB (150) ABATACEPT (136)

Which INFLIXIMAB Alternatives Have Lower Post procedural infection Risk?

INFLIXIMAB vs INFLIXIMAB-ABDA INFLIXIMAB vs INFLIXIMAB-AXXQ INFLIXIMAB vs INFLIXIMAB-DYYB INFLIXIMAB vs INFLIXIMAB-QBTX INFLIXIMAB vs INFLIXIMAB, RECOMBINANT

Related Pages

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