Does ABATACEPT Cause Device issue? 386 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 386 reports of Device issue have been filed in association with ABATACEPT (ORENCIA). This represents 0.3% of all adverse event reports for ABATACEPT.
386
Reports of Device issue with ABATACEPT
0.3%
of all ABATACEPT reports
0
Deaths
20
Hospitalizations
How Dangerous Is Device issue From ABATACEPT?
Of the 386 reports, 20 (5.2%) required hospitalization, and 3 (0.8%) were considered life-threatening.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABATACEPT. However, 386 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 issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which ABATACEPT Alternatives Have Lower Device issue Risk?
ABATACEPT vs ABATACEPT SUBQ /ML
ABATACEPT vs ABCIXIMAB
ABATACEPT vs ABEMACICLIB
ABATACEPT vs ABILIFY
ABATACEPT vs ABIRATERONE