Does ABATACEPT Cause Device defective? 458 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 458 reports of Device defective have been filed in association with ABATACEPT (ORENCIA). This represents 0.4% of all adverse event reports for ABATACEPT.
458
Reports of Device defective with ABATACEPT
0.4%
of all ABATACEPT reports
0
Deaths
9
Hospitalizations
How Dangerous Is Device defective From ABATACEPT?
Of the 458 reports, 9 (2.0%) required hospitalization.
Is Device defective Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABATACEPT. However, 458 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 Device defective?
SOMATROPIN (1,719)
USTEKINUMAB (1,071)
SECUKINUMAB (666)
GUSELKUMAB (574)
GOLIMUMAB (539)
ALBUTEROL (445)
TOCILIZUMAB (400)
INSULIN GLARGINE (397)
EXENATIDE (387)
BUDESONIDE\FORMOTEROL (378)
Which ABATACEPT Alternatives Have Lower Device defective Risk?
ABATACEPT vs ABATACEPT SUBQ /ML
ABATACEPT vs ABCIXIMAB
ABATACEPT vs ABEMACICLIB
ABATACEPT vs ABILIFY
ABATACEPT vs ABIRATERONE