Does ABATACEPT Cause Wrong technique in product usage process? 207 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 207 reports of Wrong technique in product usage process have been filed in association with ABATACEPT (ORENCIA). This represents 0.2% of all adverse event reports for ABATACEPT.
207
Reports of Wrong technique in product usage process with ABATACEPT
0.2%
of all ABATACEPT reports
2
Deaths
12
Hospitalizations
How Dangerous Is Wrong technique in product usage process From ABATACEPT?
Of the 207 reports, 2 (1.0%) resulted in death, 12 (5.8%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABATACEPT. However, 207 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which ABATACEPT Alternatives Have Lower Wrong technique in product usage process Risk?
ABATACEPT vs ABATACEPT SUBQ /ML
ABATACEPT vs ABCIXIMAB
ABATACEPT vs ABEMACICLIB
ABATACEPT vs ABILIFY
ABATACEPT vs ABIRATERONE