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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does ABATACEPT Cause Device failure? 177 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 177 reports of Device failure have been filed in association with ABATACEPT (ORENCIA). This represents 0.2% of all adverse event reports for ABATACEPT.

177
Reports of Device failure with ABATACEPT
0.2%
of all ABATACEPT reports
0
Deaths
8
Hospitalizations

How Dangerous Is Device failure From ABATACEPT?

Of the 177 reports, 8 (4.5%) required hospitalization.

Is Device failure Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ABATACEPT. However, 177 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 failure?

EPINEPHRINE (1,344) SOMATROPIN (1,141) PEGFILGRASTIM (829) TREPROSTINIL (713) BACLOFEN (691) BUDESONIDE\FORMOTEROL (686) ETANERCEPT (576) GOLIMUMAB (487) LEVONORGESTREL (332) ACLIDINIUM (304)

Which ABATACEPT Alternatives Have Lower Device failure Risk?

ABATACEPT vs ABATACEPT SUBQ /ML ABATACEPT vs ABCIXIMAB ABATACEPT vs ABEMACICLIB ABATACEPT vs ABILIFY ABATACEPT vs ABIRATERONE

Related Pages

ABATACEPT Full Profile All Device failure Reports All Drugs Causing Device failure ABATACEPT Demographics