Does ABATACEPT Cause Product dose omission? 504 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 504 reports of Product dose omission have been filed in association with ABATACEPT (ORENCIA). This represents 0.4% of all adverse event reports for ABATACEPT.
504
Reports of Product dose omission with ABATACEPT
0.4%
of all ABATACEPT reports
9
Deaths
102
Hospitalizations
How Dangerous Is Product dose omission From ABATACEPT?
Of the 504 reports, 9 (1.8%) resulted in death, 102 (20.2%) required hospitalization, and 5 (1.0%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABATACEPT. However, 504 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?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which ABATACEPT Alternatives Have Lower Product dose omission Risk?
ABATACEPT vs ABATACEPT SUBQ /ML
ABATACEPT vs ABCIXIMAB
ABATACEPT vs ABEMACICLIB
ABATACEPT vs ABILIFY
ABATACEPT vs ABIRATERONE