Does ABATACEPT Cause Incorrect product storage? 583 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 583 reports of Incorrect product storage have been filed in association with ABATACEPT (ORENCIA). This represents 0.5% of all adverse event reports for ABATACEPT.
583
Reports of Incorrect product storage with ABATACEPT
0.5%
of all ABATACEPT reports
0
Deaths
12
Hospitalizations
How Dangerous Is Incorrect product storage From ABATACEPT?
Of the 583 reports, 12 (2.1%) required hospitalization.
Is Incorrect product storage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABATACEPT. However, 583 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 Incorrect product storage?
ETANERCEPT (2,149)
INSULIN LISPRO (1,114)
TERIPARATIDE (573)
ADALIMUMAB (476)
GOLIMUMAB (392)
INSULIN GLARGINE (341)
INSULIN HUMAN (336)
USTEKINUMAB (299)
ERYTHROPOIETIN (268)
CYCLOSPORINE (203)
Which ABATACEPT Alternatives Have Lower Incorrect product storage Risk?
ABATACEPT vs ABATACEPT SUBQ /ML
ABATACEPT vs ABCIXIMAB
ABATACEPT vs ABEMACICLIB
ABATACEPT vs ABILIFY
ABATACEPT vs ABIRATERONE