Does INFLIXIMAB Cause Intentional product use issue? 11,028 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11,028 reports of Intentional product use issue have been filed in association with INFLIXIMAB (Renflexis). This represents 7.9% of all adverse event reports for INFLIXIMAB.
11,028
Reports of Intentional product use issue with INFLIXIMAB
7.9%
of all INFLIXIMAB reports
1,280
Deaths
3,261
Hospitalizations
How Dangerous Is Intentional product use issue From INFLIXIMAB?
Of the 11,028 reports, 1,280 (11.6%) resulted in death, 3,261 (29.6%) required hospitalization, and 1,489 (13.5%) 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. However, 11,028 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 use issue?
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)
HYDROXYCHLOROQUINE (3,059)
Which INFLIXIMAB Alternatives Have Lower Intentional product use issue Risk?
INFLIXIMAB vs INFLIXIMAB-ABDA
INFLIXIMAB vs INFLIXIMAB-AXXQ
INFLIXIMAB vs INFLIXIMAB-DYYB
INFLIXIMAB vs INFLIXIMAB-QBTX
INFLIXIMAB vs INFLIXIMAB, RECOMBINANT