Does ABATACEPT Cause Product quality issue? 899 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 899 reports of Product quality issue have been filed in association with ABATACEPT (ORENCIA). This represents 0.8% of all adverse event reports for ABATACEPT.
899
Reports of Product quality issue with ABATACEPT
0.8%
of all ABATACEPT reports
486
Deaths
472
Hospitalizations
How Dangerous Is Product quality issue From ABATACEPT?
Of the 899 reports, 486 (54.1%) resulted in death, 472 (52.5%) required hospitalization, and 484 (53.8%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABATACEPT. However, 899 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which ABATACEPT Alternatives Have Lower Product quality issue Risk?
ABATACEPT vs ABATACEPT SUBQ /ML
ABATACEPT vs ABCIXIMAB
ABATACEPT vs ABEMACICLIB
ABATACEPT vs ABILIFY
ABATACEPT vs ABIRATERONE