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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 SPARTALIZUMAB Cause Device leakage? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Device leakage have been filed in association with SPARTALIZUMAB. This represents 2.1% of all adverse event reports for SPARTALIZUMAB.

6
Reports of Device leakage with SPARTALIZUMAB
2.1%
of all SPARTALIZUMAB reports
0
Deaths
6
Hospitalizations

How Dangerous Is Device leakage From SPARTALIZUMAB?

Of the 6 reports, 6 (100.0%) required hospitalization.

Is Device leakage Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SPARTALIZUMAB. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does SPARTALIZUMAB Cause?

Pyrexia (29) Diarrhoea (17) Vomiting (17) General physical health deterioration (14) Colitis (12) Dyspnoea (12) Febrile neutropenia (12) Pneumonitis (12) Acute kidney injury (11) Nausea (10)

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 SPARTALIZUMAB Alternatives Have Lower Device leakage Risk?

SPARTALIZUMAB vs SPIRIVA SPARTALIZUMAB vs SPIRONOLACTONE SPARTALIZUMAB vs SPRYCEL SPARTALIZUMAB vs STIVARGA SPARTALIZUMAB vs STREPTOZOCIN

Related Pages

SPARTALIZUMAB Full Profile All Device leakage Reports All Drugs Causing Device leakage SPARTALIZUMAB Demographics