Does ABATACEPT Cause Therapeutic product effect decreased? 7,256 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7,256 reports of Therapeutic product effect decreased have been filed in association with ABATACEPT (ORENCIA). This represents 6.3% of all adverse event reports for ABATACEPT.
7,256
Reports of Therapeutic product effect decreased with ABATACEPT
6.3%
of all ABATACEPT reports
900
Deaths
2,465
Hospitalizations
How Dangerous Is Therapeutic product effect decreased From ABATACEPT?
Of the 7,256 reports, 900 (12.4%) resulted in death, 2,465 (34.0%) required hospitalization, and 1,314 (18.1%) were considered life-threatening.
Is Therapeutic product effect decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABATACEPT. However, 7,256 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 Therapeutic product effect decreased?
ADALIMUMAB (11,058)
METHOTREXATE (8,952)
ETANERCEPT (8,819)
TOCILIZUMAB (7,208)
LEFLUNOMIDE (7,025)
HYDROXYCHLOROQUINE (6,450)
INFLIXIMAB (6,401)
RITUXIMAB (6,281)
GOLIMUMAB (5,478)
SULFASALAZINE (5,386)
Which ABATACEPT Alternatives Have Lower Therapeutic product effect decreased Risk?
ABATACEPT vs ABATACEPT SUBQ /ML
ABATACEPT vs ABCIXIMAB
ABATACEPT vs ABEMACICLIB
ABATACEPT vs ABILIFY
ABATACEPT vs ABIRATERONE