Does ABATACEPT Cause Product use in unapproved indication? 2,392 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,392 reports of Product use in unapproved indication have been filed in association with ABATACEPT (ORENCIA). This represents 2.1% of all adverse event reports for ABATACEPT.
2,392
Reports of Product use in unapproved indication with ABATACEPT
2.1%
of all ABATACEPT reports
1,008
Deaths
1,311
Hospitalizations
How Dangerous Is Product use in unapproved indication From ABATACEPT?
Of the 2,392 reports, 1,008 (42.1%) resulted in death, 1,311 (54.8%) required hospitalization, and 1,253 (52.4%) were considered life-threatening.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABATACEPT. However, 2,392 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 use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
Which ABATACEPT Alternatives Have Lower Product use in unapproved indication Risk?
ABATACEPT vs ABATACEPT SUBQ /ML
ABATACEPT vs ABCIXIMAB
ABATACEPT vs ABEMACICLIB
ABATACEPT vs ABILIFY
ABATACEPT vs ABIRATERONE