Does INFLIXIMAB Cause Intentional product misuse? 498 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 498 reports of Intentional product misuse have been filed in association with INFLIXIMAB (Renflexis). This represents 0.4% of all adverse event reports for INFLIXIMAB.
498
Reports of Intentional product misuse with INFLIXIMAB
0.4%
of all INFLIXIMAB reports
170
Deaths
135
Hospitalizations
How Dangerous Is Intentional product misuse From INFLIXIMAB?
Of the 498 reports, 170 (34.1%) resulted in death, 135 (27.1%) required hospitalization, and 87 (17.5%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INFLIXIMAB. However, 498 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which INFLIXIMAB Alternatives Have Lower Intentional product misuse Risk?
INFLIXIMAB vs INFLIXIMAB-ABDA
INFLIXIMAB vs INFLIXIMAB-AXXQ
INFLIXIMAB vs INFLIXIMAB-DYYB
INFLIXIMAB vs INFLIXIMAB-QBTX
INFLIXIMAB vs INFLIXIMAB, RECOMBINANT