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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 use error? 39 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 39 reports of Device use error have been filed in association with ABATACEPT (ORENCIA). This represents 0.0% of all adverse event reports for ABATACEPT.

39
Reports of Device use error with ABATACEPT
0.0%
of all ABATACEPT reports
0
Deaths
1
Hospitalizations

How Dangerous Is Device use error From ABATACEPT?

Of the 39 reports, 1 (2.6%) required hospitalization.

Is Device use error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ABATACEPT. However, 39 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 use error?

PEGFILGRASTIM (6,001) ALBUTEROL (5,215) ALBIGLUTIDE (4,056) EVOLOCUMAB (4,002) SOMATROPIN (2,801) FLUTICASONE\SALMETEROL (1,749) FLUTICASONE (783) FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (766) ERENUMAB-AOOE (711) ETANERCEPT (665)

Which ABATACEPT Alternatives Have Lower Device use error 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 use error Reports All Drugs Causing Device use error ABATACEPT Demographics