Does INFLIXIMAB Cause Adverse event? 2,269 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,269 reports of Adverse event have been filed in association with INFLIXIMAB (Renflexis). This represents 1.6% of all adverse event reports for INFLIXIMAB.
2,269
Reports of Adverse event with INFLIXIMAB
1.6%
of all INFLIXIMAB reports
448
Deaths
763
Hospitalizations
How Dangerous Is Adverse event From INFLIXIMAB?
Of the 2,269 reports, 448 (19.7%) resulted in death, 763 (33.6%) required hospitalization, and 532 (23.4%) were considered life-threatening.
Is Adverse event Listed in the Official Label?
Yes, Adverse event is listed as a known adverse reaction in the official FDA drug label for INFLIXIMAB.
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 Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
RISPERIDONE (1,440)
Which INFLIXIMAB Alternatives Have Lower Adverse event Risk?
INFLIXIMAB vs INFLIXIMAB-ABDA
INFLIXIMAB vs INFLIXIMAB-AXXQ
INFLIXIMAB vs INFLIXIMAB-DYYB
INFLIXIMAB vs INFLIXIMAB-QBTX
INFLIXIMAB vs INFLIXIMAB, RECOMBINANT