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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 Hepatic steatosis? 345 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 345 reports of Hepatic steatosis have been filed in association with ABATACEPT (ORENCIA). This represents 0.3% of all adverse event reports for ABATACEPT.

345
Reports of Hepatic steatosis with ABATACEPT
0.3%
of all ABATACEPT reports
2
Deaths
109
Hospitalizations

How Dangerous Is Hepatic steatosis From ABATACEPT?

Of the 345 reports, 2 (0.6%) resulted in death, 109 (31.6%) required hospitalization, and 6 (1.7%) were considered life-threatening.

Is Hepatic steatosis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ABATACEPT. However, 345 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 Hepatic steatosis?

METHOTREXATE (1,400) ADALIMUMAB (1,058) ETANERCEPT (620) TOCILIZUMAB (476) TOFACITINIB (405) LEFLUNOMIDE (359) HYDROXYCHLOROQUINE (358) METFORMIN (343) INFLIXIMAB (325) SECUKINUMAB (308)

Which ABATACEPT Alternatives Have Lower Hepatic steatosis Risk?

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

Related Pages

ABATACEPT Full Profile All Hepatic steatosis Reports All Drugs Causing Hepatic steatosis ABATACEPT Demographics