Does ABATACEPT Cause Device malfunction? 2,459 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,459 reports of Device malfunction have been filed in association with ABATACEPT (ORENCIA). This represents 2.1% of all adverse event reports for ABATACEPT.
2,459
Reports of Device malfunction with ABATACEPT
2.1%
of all ABATACEPT reports
5
Deaths
89
Hospitalizations
How Dangerous Is Device malfunction From ABATACEPT?
Of the 2,459 reports, 5 (0.2%) resulted in death, 89 (3.6%) required hospitalization, and 3 (0.1%) were considered life-threatening.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABATACEPT. However, 2,459 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 malfunction?
PEGFILGRASTIM (6,818)
EXENATIDE (3,273)
BUDESONIDE\FORMOTEROL (2,771)
SOMATROPIN (2,311)
GOLIMUMAB (2,293)
SECUKINUMAB (2,259)
ALBUTEROL (2,257)
GUSELKUMAB (1,410)
MOMETASONE FUROATE (1,332)
ACLIDINIUM (1,325)
Which ABATACEPT Alternatives Have Lower Device malfunction Risk?
ABATACEPT vs ABATACEPT SUBQ /ML
ABATACEPT vs ABCIXIMAB
ABATACEPT vs ABEMACICLIB
ABATACEPT vs ABILIFY
ABATACEPT vs ABIRATERONE