Does ADALIMUMAB-FKJP Cause Device delivery system issue? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Device delivery system issue have been filed in association with ADALIMUMAB-FKJP (Adalimumab). This represents 0.4% of all adverse event reports for ADALIMUMAB-FKJP.
7
Reports of Device delivery system issue with ADALIMUMAB-FKJP
0.4%
of all ADALIMUMAB-FKJP reports
0
Deaths
3
Hospitalizations
How Dangerous Is Device delivery system issue From ADALIMUMAB-FKJP?
Of the 7 reports, 3 (42.9%) required hospitalization.
Is Device delivery system issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ADALIMUMAB-FKJP. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does ADALIMUMAB-FKJP Cause?
Off label use (287)
Drug ineffective (285)
Product dose omission issue (156)
Rheumatoid arthritis (113)
Crohn's disease (110)
Inappropriate schedule of product administration (105)
Diarrhoea (103)
Pain (100)
Covid-19 (84)
Arthralgia (80)
What Other Drugs Cause Device delivery system issue?
ALBUTEROL (9,509)
SOMATROPIN (1,848)
EXENATIDE (1,533)
BUDESONIDE\FORMOTEROL (1,260)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (1,181)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (523)
LEVALBUTEROL (459)
MOMETASONE FUROATE\OLOPATADINE (347)
ABATACEPT (342)
PEGFILGRASTIM (323)
Which ADALIMUMAB-FKJP Alternatives Have Lower Device delivery system issue Risk?
ADALIMUMAB-FKJP vs ADALIMUMAB-RYVK
ADALIMUMAB-FKJP vs ADALIMUMAB\ISOPROPYL ALCOHOL
ADALIMUMAB-FKJP vs ADAPALENE
ADALIMUMAB-FKJP vs ADAPALENE\BENZOYL PEROXIDE
ADALIMUMAB-FKJP vs ADCETRIS