Does INFLIXIMAB Cause Intentional dose omission? 815 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 815 reports of Intentional dose omission have been filed in association with INFLIXIMAB (Renflexis). This represents 0.6% of all adverse event reports for INFLIXIMAB.
815
Reports of Intentional dose omission with INFLIXIMAB
0.6%
of all INFLIXIMAB reports
13
Deaths
244
Hospitalizations
How Dangerous Is Intentional dose omission From INFLIXIMAB?
Of the 815 reports, 13 (1.6%) resulted in death, 244 (29.9%) required hospitalization, and 10 (1.2%) were considered life-threatening.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INFLIXIMAB. However, 815 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 dose omission?
DUPILUMAB (2,269)
CERTOLIZUMAB PEGOL (1,253)
ADALIMUMAB (845)
TOFACITINIB (845)
ABALOPARATIDE (623)
ETANERCEPT (615)
AMBRISENTAN (595)
SODIUM OXYBATE (580)
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)
SOFOSBUVIR\VELPATASVIR (474)
Which INFLIXIMAB Alternatives Have Lower Intentional dose omission Risk?
INFLIXIMAB vs INFLIXIMAB-ABDA
INFLIXIMAB vs INFLIXIMAB-AXXQ
INFLIXIMAB vs INFLIXIMAB-DYYB
INFLIXIMAB vs INFLIXIMAB-QBTX
INFLIXIMAB vs INFLIXIMAB, RECOMBINANT