Does NEMOLIZUMAB-ILTO Cause Device breakage? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Device breakage have been filed in association with NEMOLIZUMAB-ILTO. This represents 0.2% of all adverse event reports for NEMOLIZUMAB-ILTO.
7
Reports of Device breakage with NEMOLIZUMAB-ILTO
0.2%
of all NEMOLIZUMAB-ILTO reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device breakage From NEMOLIZUMAB-ILTO?
Of the 7 reports.
Is Device breakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NEMOLIZUMAB-ILTO. However, 7 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)
Device malfunction (761)
Incorrect dose administered (579)
Pruritus (416)
Rash (263)
Headache (181)
Drug ineffective (158)
Device leakage (153)
Device use issue (120)
What Other Drugs Cause Device breakage?
COPPER (9,201)
SOMATROPIN (7,761)
ETONOGESTREL (4,140)
LEVONORGESTREL (2,726)
ETHINYL ESTRADIOL\ETONOGESTREL (741)
CARBIDOPA\LEVODOPA (634)
TREPROSTINIL (396)
ADALIMUMAB (375)
ALBUTEROL (256)
EPOPROSTENOL (240)
Which NEMOLIZUMAB-ILTO Alternatives Have Lower Device breakage Risk?
NEMOLIZUMAB-ILTO vs NEOMYCIN
NEMOLIZUMAB-ILTO vs NEORAL
NEMOLIZUMAB-ILTO vs NEOSTIGMINE
NEMOLIZUMAB-ILTO vs NEOSTIGMINE METHYLSULFATE
NEMOLIZUMAB-ILTO vs NEPAFENAC