Does ABATACEPT Cause Incorrect product administration duration? 69 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 69 reports of Incorrect product administration duration have been filed in association with ABATACEPT (ORENCIA). This represents 0.1% of all adverse event reports for ABATACEPT.
69
Reports of Incorrect product administration duration with ABATACEPT
0.1%
of all ABATACEPT reports
55
Deaths
58
Hospitalizations
How Dangerous Is Incorrect product administration duration From ABATACEPT?
Of the 69 reports, 55 (79.7%) resulted in death, 58 (84.1%) required hospitalization, and 56 (81.2%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABATACEPT. However, 69 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 administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which ABATACEPT Alternatives Have Lower Incorrect product administration duration Risk?
ABATACEPT vs ABATACEPT SUBQ /ML
ABATACEPT vs ABCIXIMAB
ABATACEPT vs ABEMACICLIB
ABATACEPT vs ABILIFY
ABATACEPT vs ABIRATERONE