Does ADALIMUMAB-AFZB Cause Device breakage? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Device breakage have been filed in association with ADALIMUMAB-AFZB (ABRILADA). This represents 0.8% of all adverse event reports for ADALIMUMAB-AFZB.
16
Reports of Device breakage with ADALIMUMAB-AFZB
0.8%
of all ADALIMUMAB-AFZB reports
1
Deaths
1
Hospitalizations
How Dangerous Is Device breakage From ADALIMUMAB-AFZB?
Of the 16 reports, 1 (6.3%) resulted in death, 1 (6.3%) required hospitalization.
Is Device breakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ADALIMUMAB-AFZB. However, 16 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 breakage?
COPPER (9,201)
SOMATROPIN (7,761)
ETONOGESTREL (4,140)
LEVONORGESTREL (2,726)
ETHINYL ESTRADIOL\ETONOGESTREL (741)
CARBIDOPA\LEVODOPA (634)
TREPROSTINIL (396)
ADALIMUMAB (375)
ALBUTEROL (256)
EPOPROSTENOL (240)
Which ADALIMUMAB-AFZB Alternatives Have Lower Device breakage 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