Does ABATACEPT Cause Intentional product misuse? 439 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 439 reports of Intentional product misuse have been filed in association with ABATACEPT (ORENCIA). This represents 0.4% of all adverse event reports for ABATACEPT.
439
Reports of Intentional product misuse with ABATACEPT
0.4%
of all ABATACEPT reports
169
Deaths
108
Hospitalizations
How Dangerous Is Intentional product misuse From ABATACEPT?
Of the 439 reports, 169 (38.5%) resulted in death, 108 (24.6%) required hospitalization, and 82 (18.7%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABATACEPT. However, 439 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 product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which ABATACEPT Alternatives Have Lower Intentional product misuse Risk?
ABATACEPT vs ABATACEPT SUBQ /ML
ABATACEPT vs ABCIXIMAB
ABATACEPT vs ABEMACICLIB
ABATACEPT vs ABILIFY
ABATACEPT vs ABIRATERONE