Does ADALIMUMAB-AQVH Cause Device malfunction? 18 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Device malfunction have been filed in association with ADALIMUMAB-AQVH. This represents 24.0% of all adverse event reports for ADALIMUMAB-AQVH.
18
Reports of Device malfunction with ADALIMUMAB-AQVH
24.0%
of all ADALIMUMAB-AQVH reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device malfunction From ADALIMUMAB-AQVH?
Of the 18 reports.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ADALIMUMAB-AQVH. However, 18 reports have been filed with the FAERS database.
What Other Side Effects Does ADALIMUMAB-AQVH Cause?
Accidental exposure to product (32)
Product dose omission issue (21)
No adverse event (8)
Product quality issue (7)
Product complaint (6)
Device leakage (5)
Drug ineffective (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)