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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does NEMOLIZUMAB-ILTO Cause Device leakage? 153 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 153 reports of Device leakage have been filed in association with NEMOLIZUMAB-ILTO. This represents 3.7% of all adverse event reports for NEMOLIZUMAB-ILTO.

153
Reports of Device leakage with NEMOLIZUMAB-ILTO
3.7%
of all NEMOLIZUMAB-ILTO reports
0
Deaths
1
Hospitalizations

How Dangerous Is Device leakage From NEMOLIZUMAB-ILTO?

Of the 153 reports, 1 (0.7%) required hospitalization.

Is Device leakage Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for NEMOLIZUMAB-ILTO. However, 153 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 use issue (120) Dermatitis atopic (117)

What Other Drugs Cause Device leakage?

SOMATROPIN (9,113) LEUPROLIDE (5,861) EXENATIDE (5,115) PEGFILGRASTIM (1,380) ALBIGLUTIDE (1,195) SECUKINUMAB (910) RISPERIDONE (878) TREPROSTINIL (874) DEVICE (795) GUSELKUMAB (712)

Which NEMOLIZUMAB-ILTO Alternatives Have Lower Device leakage Risk?

NEMOLIZUMAB-ILTO vs NEOMYCIN NEMOLIZUMAB-ILTO vs NEORAL NEMOLIZUMAB-ILTO vs NEOSTIGMINE NEMOLIZUMAB-ILTO vs NEOSTIGMINE METHYLSULFATE NEMOLIZUMAB-ILTO vs NEPAFENAC

Related Pages

NEMOLIZUMAB-ILTO Full Profile All Device leakage Reports All Drugs Causing Device leakage NEMOLIZUMAB-ILTO Demographics