Does ABATACEPT Cause Intentional dose omission? 252 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 252 reports of Intentional dose omission have been filed in association with ABATACEPT (ORENCIA). This represents 0.2% of all adverse event reports for ABATACEPT.
252
Reports of Intentional dose omission with ABATACEPT
0.2%
of all ABATACEPT reports
3
Deaths
31
Hospitalizations
How Dangerous Is Intentional dose omission From ABATACEPT?
Of the 252 reports, 3 (1.2%) resulted in death, 31 (12.3%) required hospitalization, and 3 (1.2%) were considered life-threatening.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABATACEPT. However, 252 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 Intentional dose omission?
DUPILUMAB (2,269)
CERTOLIZUMAB PEGOL (1,253)
ADALIMUMAB (845)
TOFACITINIB (845)
INFLIXIMAB (815)
ABALOPARATIDE (623)
ETANERCEPT (615)
AMBRISENTAN (595)
SODIUM OXYBATE (580)
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)
Which ABATACEPT Alternatives Have Lower Intentional dose omission Risk?
ABATACEPT vs ABATACEPT SUBQ /ML
ABATACEPT vs ABCIXIMAB
ABATACEPT vs ABEMACICLIB
ABATACEPT vs ABILIFY
ABATACEPT vs ABIRATERONE