Does NEMOLIZUMAB-ILTO Cause Device malfunction? 761 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 761 reports of Device malfunction have been filed in association with NEMOLIZUMAB-ILTO. This represents 18.2% of all adverse event reports for NEMOLIZUMAB-ILTO.
761
Reports of Device malfunction with NEMOLIZUMAB-ILTO
18.2%
of all NEMOLIZUMAB-ILTO reports
0
Deaths
1
Hospitalizations
How Dangerous Is Device malfunction From NEMOLIZUMAB-ILTO?
Of the 761 reports, 1 (0.1%) required hospitalization.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NEMOLIZUMAB-ILTO. However, 761 reports have been filed with the FAERS database.
What Other Side Effects Does NEMOLIZUMAB-ILTO Cause?
Inappropriate schedule of product administration (826)
Product dose omission issue (792)
Incorrect dose administered (579)
Pruritus (416)
Rash (263)
Headache (181)
Drug ineffective (158)
Device leakage (153)
Device use issue (120)
Dermatitis atopic (117)
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 NEMOLIZUMAB-ILTO Alternatives Have Lower Device malfunction Risk?
NEMOLIZUMAB-ILTO vs NEOMYCIN
NEMOLIZUMAB-ILTO vs NEORAL
NEMOLIZUMAB-ILTO vs NEOSTIGMINE
NEMOLIZUMAB-ILTO vs NEOSTIGMINE METHYLSULFATE
NEMOLIZUMAB-ILTO vs NEPAFENAC