Does ABATACEPT Cause Product dose omission in error? 86 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 86 reports of Product dose omission in error have been filed in association with ABATACEPT (ORENCIA). This represents 0.1% of all adverse event reports for ABATACEPT.
86
Reports of Product dose omission in error with ABATACEPT
0.1%
of all ABATACEPT reports
0
Deaths
4
Hospitalizations
How Dangerous Is Product dose omission in error From ABATACEPT?
Of the 86 reports, 4 (4.7%) required hospitalization, and 1 (1.2%) were considered life-threatening.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABATACEPT. However, 86 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 Product dose omission in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which ABATACEPT Alternatives Have Lower Product dose omission in error Risk?
ABATACEPT vs ABATACEPT SUBQ /ML
ABATACEPT vs ABCIXIMAB
ABATACEPT vs ABEMACICLIB
ABATACEPT vs ABILIFY
ABATACEPT vs ABIRATERONE