Does INFLIXIMAB-ABDA Cause Intentional product use issue? 17 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Intentional product use issue have been filed in association with INFLIXIMAB-ABDA. This represents 0.9% of all adverse event reports for INFLIXIMAB-ABDA.
17
Reports of Intentional product use issue with INFLIXIMAB-ABDA
0.9%
of all INFLIXIMAB-ABDA reports
1
Deaths
6
Hospitalizations
How Dangerous Is Intentional product use issue From INFLIXIMAB-ABDA?
Of the 17 reports, 1 (5.9%) resulted in death, 6 (35.3%) required hospitalization, and 1 (5.9%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INFLIXIMAB-ABDA. However, 17 reports have been filed with the FAERS database.
What Other Side Effects Does INFLIXIMAB-ABDA Cause?
Off label use (493)
Product use issue (272)
Dyspnoea (145)
Nausea (142)
Crohn's disease (133)
Arthralgia (131)
Diarrhoea (118)
Drug ineffective (111)
Headache (111)
Malaise (111)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which INFLIXIMAB-ABDA Alternatives Have Lower Intentional product use issue Risk?
INFLIXIMAB-ABDA vs INFLIXIMAB-AXXQ
INFLIXIMAB-ABDA vs INFLIXIMAB-DYYB
INFLIXIMAB-ABDA vs INFLIXIMAB-QBTX
INFLIXIMAB-ABDA vs INFLIXIMAB, RECOMBINANT
INFLIXIMAB-ABDA vs INFLUENZA A VIRUS A/CALIFORNIA/7/2009 LIVE ANTIGEN\INFLUENZA A VIRUS A/TEXAS/50/2012 LIVE ANTIGEN\INFLUENZA B VIRUS B/BRISBANE/60/2008 LIVE ANTIGEN\INFLUENZA B VIRUS B/MASSACHUSETTS/2/2012 LIVE ANTIGEN