Does HUMIRA Cause Device malfunction? 1,212 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,212 reports of Device malfunction have been filed in association with HUMIRA. This represents 3.1% of all adverse event reports for HUMIRA.
1,212
Reports of Device malfunction with HUMIRA
3.1%
of all HUMIRA reports
0
Deaths
20
Hospitalizations
How Dangerous Is Device malfunction From HUMIRA?
Of the 1,212 reports, 20 (1.7%) required hospitalization.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for HUMIRA. However, 1,212 reports have been filed with the FAERS database.
What Other Side Effects Does HUMIRA Cause?
Injection site pain (6,005)
Drug ineffective (3,506)
Arthralgia (2,204)
Pain (2,045)
Fatigue (1,868)
Psoriasis (1,857)
Injection site erythema (1,654)
Injection site bruising (1,623)
Headache (1,582)
Nasopharyngitis (1,552)
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 HUMIRA Alternatives Have Lower Device malfunction Risk?
HUMIRA vs HUMIRA PEN
HUMIRA vs HYALURONATE
HUMIRA vs HYALURONIC ACID
HUMIRA vs HYALURONIC ACID\LIDOCAINE
HUMIRA vs HYALURONIDASE