Does ADALIMUMAB-AFZB Cause Device defective? 40 Reports in FDA Database
Grow Your Own Natural Pharmacy at Home
Medicinal Garden Kit — 10 healing herbs, 4,818 seeds + step-by-step guide.
According to the FDA Adverse Event Reporting System (FAERS), 40 reports of Device defective have been filed in association with ADALIMUMAB-AFZB (ABRILADA). This represents 1.9% of all adverse event reports for ADALIMUMAB-AFZB.
40
Reports of Device defective with ADALIMUMAB-AFZB
1.9%
of all ADALIMUMAB-AFZB reports
0
Deaths
2
Hospitalizations
How Dangerous Is Device defective From ADALIMUMAB-AFZB?
Of the 40 reports, 2 (5.0%) required hospitalization.
Is Device defective Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ADALIMUMAB-AFZB. However, 40 reports have been filed with the FAERS database.
What Other Side Effects Does ADALIMUMAB-AFZB Cause?
Off label use (748)
Condition aggravated (533)
Drug ineffective (254)
Fatigue (231)
Arthralgia (190)
Pain (170)
Injection site pain (159)
Drug dose omission by device (116)
Nausea (115)
Headache (113)
What Other Drugs Cause Device defective?
SOMATROPIN (1,719)
USTEKINUMAB (1,071)
SECUKINUMAB (666)
GUSELKUMAB (574)
GOLIMUMAB (539)
ABATACEPT (458)
ALBUTEROL (445)
TOCILIZUMAB (400)
INSULIN GLARGINE (397)
EXENATIDE (387)
Which ADALIMUMAB-AFZB Alternatives Have Lower Device defective Risk?
ADALIMUMAB-AFZB vs ADALIMUMAB-ATTO
ADALIMUMAB-AFZB vs ADALIMUMAB-BWWD
ADALIMUMAB-AFZB vs ADALIMUMAB-FKJP
ADALIMUMAB-AFZB vs ADALIMUMAB-RYVK
ADALIMUMAB-AFZB vs ADALIMUMAB\ISOPROPYL ALCOHOL