Does ABATACEPT Cause Intentional product use issue? 3,693 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 3,693 reports of Intentional product use issue have been filed in association with ABATACEPT (ORENCIA). This represents 3.2% of all adverse event reports for ABATACEPT.
3,693
Reports of Intentional product use issue with ABATACEPT
3.2%
of all ABATACEPT reports
1,146
Deaths
1,645
Hospitalizations
How Dangerous Is Intentional product use issue From ABATACEPT?
Of the 3,693 reports, 1,146 (31.0%) resulted in death, 1,645 (44.5%) required hospitalization, and 1,427 (38.6%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABATACEPT. However, 3,693 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 use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
HYDROXYCHLOROQUINE (3,059)
Which ABATACEPT Alternatives Have Lower Intentional product use issue Risk?
ABATACEPT vs ABATACEPT SUBQ /ML
ABATACEPT vs ABCIXIMAB
ABATACEPT vs ABEMACICLIB
ABATACEPT vs ABILIFY
ABATACEPT vs ABIRATERONE