Does ABATACEPT Cause Device delivery system issue? 342 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 342 reports of Device delivery system issue have been filed in association with ABATACEPT (ORENCIA). This represents 0.3% of all adverse event reports for ABATACEPT.
342
Reports of Device delivery system issue with ABATACEPT
0.3%
of all ABATACEPT reports
0
Deaths
4
Hospitalizations
How Dangerous Is Device delivery system issue From ABATACEPT?
Of the 342 reports, 4 (1.2%) required hospitalization.
Is Device delivery system issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABATACEPT. However, 342 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 delivery system issue?
ALBUTEROL (9,509)
SOMATROPIN (1,848)
EXENATIDE (1,533)
BUDESONIDE\FORMOTEROL (1,260)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (1,181)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (523)
LEVALBUTEROL (459)
MOMETASONE FUROATE\OLOPATADINE (347)
PEGFILGRASTIM (323)
ALBUTEROL\BUDESONIDE (244)
Which ABATACEPT Alternatives Have Lower Device delivery system issue Risk?
ABATACEPT vs ABATACEPT SUBQ /ML
ABATACEPT vs ABCIXIMAB
ABATACEPT vs ABEMACICLIB
ABATACEPT vs ABILIFY
ABATACEPT vs ABIRATERONE