Does ADALIMUMAB-ADBM Cause Device malfunction? 15 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Device malfunction have been filed in association with ADALIMUMAB-ADBM (Adalimumab-adbm). This represents 14.2% of all adverse event reports for ADALIMUMAB-ADBM.
15
Reports of Device malfunction with ADALIMUMAB-ADBM
14.2%
of all ADALIMUMAB-ADBM reports
0
Deaths
1
Hospitalizations
How Dangerous Is Device malfunction From ADALIMUMAB-ADBM?
Of the 15 reports, 1 (6.7%) required hospitalization.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ADALIMUMAB-ADBM. However, 15 reports have been filed with the FAERS database.
What Other Side Effects Does ADALIMUMAB-ADBM Cause?
Wrong technique in product usage process (9)
Drug ineffective (8)
Injection site pain (8)
Haemorrhage (7)
Injection site haemorrhage (7)
Diarrhoea (5)
Pain (5)
What Other Drugs Cause Device malfunction?
PEGFILGRASTIM (6,818)
EXENATIDE (3,273)
BUDESONIDE\FORMOTEROL (2,771)
ABATACEPT (2,459)
SOMATROPIN (2,311)
GOLIMUMAB (2,293)
SECUKINUMAB (2,259)
ALBUTEROL (2,257)
GUSELKUMAB (1,410)
MOMETASONE FUROATE (1,332)
Which ADALIMUMAB-ADBM Alternatives Have Lower Device malfunction Risk?
ADALIMUMAB-ADBM vs ADALIMUMAB-AFZB
ADALIMUMAB-ADBM vs ADALIMUMAB-ATTO
ADALIMUMAB-ADBM vs ADALIMUMAB-BWWD
ADALIMUMAB-ADBM vs ADALIMUMAB-FKJP
ADALIMUMAB-ADBM vs ADALIMUMAB-RYVK