Does ABATACEPT Cause Product storage error? 2,101 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,101 reports of Product storage error have been filed in association with ABATACEPT (ORENCIA). This represents 1.8% of all adverse event reports for ABATACEPT.
2,101
Reports of Product storage error with ABATACEPT
1.8%
of all ABATACEPT reports
3
Deaths
108
Hospitalizations
How Dangerous Is Product storage error From ABATACEPT?
Of the 2,101 reports, 3 (0.1%) resulted in death, 108 (5.1%) required hospitalization, and 3 (0.1%) were considered life-threatening.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABATACEPT. However, 2,101 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 storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
USTEKINUMAB (1,338)
Which ABATACEPT Alternatives Have Lower Product storage error Risk?
ABATACEPT vs ABATACEPT SUBQ /ML
ABATACEPT vs ABCIXIMAB
ABATACEPT vs ABEMACICLIB
ABATACEPT vs ABILIFY
ABATACEPT vs ABIRATERONE