Does ABATACEPT Cause Device material issue? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Device material issue have been filed in association with ABATACEPT (ORENCIA). This represents 0.0% of all adverse event reports for ABATACEPT.
14
Reports of Device material issue with ABATACEPT
0.0%
of all ABATACEPT reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device material issue From ABATACEPT?
Of the 14 reports.
Is Device material issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABATACEPT. However, 14 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 material issue?
COPPER (603)
SOMATROPIN (472)
CARBIDOPA\LEVODOPA (68)
ADALIMUMAB (62)
ESTRADIOL (51)
PEGFILGRASTIM (33)
ESTRADIOL\LEVONORGESTREL (24)
LEVONORGESTREL (13)
BACLOFEN (11)
METHOTREXATE (9)
Which ABATACEPT Alternatives Have Lower Device material issue Risk?
ABATACEPT vs ABATACEPT SUBQ /ML
ABATACEPT vs ABCIXIMAB
ABATACEPT vs ABEMACICLIB
ABATACEPT vs ABILIFY
ABATACEPT vs ABIRATERONE