Does ABATACEPT Cause Product administration interrupted? 35 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 35 reports of Product administration interrupted have been filed in association with ABATACEPT (ORENCIA). This represents 0.0% of all adverse event reports for ABATACEPT.
35
Reports of Product administration interrupted with ABATACEPT
0.0%
of all ABATACEPT reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product administration interrupted From ABATACEPT?
Of the 35 reports, 1 (2.9%) required hospitalization, and 2 (5.7%) were considered life-threatening.
Is Product administration interrupted Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABATACEPT. However, 35 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 administration interrupted?
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (1,446)
SODIUM OXYBATE (1,272)
CANNABIDIOL (511)
ISOTRETINOIN (503)
APREMILAST (314)
TREPROSTINIL (295)
EPOPROSTENOL (205)
LENALIDOMIDE (146)
ETANERCEPT (142)
INTERFERON BETA-1A (115)
Which ABATACEPT Alternatives Have Lower Product administration interrupted Risk?
ABATACEPT vs ABATACEPT SUBQ /ML
ABATACEPT vs ABCIXIMAB
ABATACEPT vs ABEMACICLIB
ABATACEPT vs ABILIFY
ABATACEPT vs ABIRATERONE