Does ABATACEPT Cause Product use issue? 5,915 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5,915 reports of Product use issue have been filed in association with ABATACEPT (ORENCIA). This represents 5.1% of all adverse event reports for ABATACEPT.
5,915
Reports of Product use issue with ABATACEPT
5.1%
of all ABATACEPT reports
874
Deaths
1,759
Hospitalizations
How Dangerous Is Product use issue From ABATACEPT?
Of the 5,915 reports, 874 (14.8%) resulted in death, 1,759 (29.7%) required hospitalization, and 1,203 (20.3%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABATACEPT. However, 5,915 reports have been filed with the FAERS database.
What Other Side Effects Does ABATACEPT Cause?
Drug ineffective (35,212)
Rheumatoid arthritis (21,898)
Pain (19,783)
Arthralgia (18,536)
Joint swelling (18,453)
Contraindicated product administered (13,559)
Fatigue (13,087)
Drug intolerance (12,451)
Rash (12,168)
Arthropathy (11,099)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
CETIRIZINE (5,771)
Which ABATACEPT Alternatives Have Lower Product use issue Risk?
ABATACEPT vs ABATACEPT SUBQ /ML
ABATACEPT vs ABCIXIMAB
ABATACEPT vs ABEMACICLIB
ABATACEPT vs ABILIFY
ABATACEPT vs ABIRATERONE