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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 DEVICE Cause Device leakage? 795 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 795 reports of Device leakage have been filed in association with DEVICE. This represents 6.2% of all adverse event reports for DEVICE.

795
Reports of Device leakage with DEVICE
6.2%
of all DEVICE reports
0
Deaths
9
Hospitalizations

How Dangerous Is Device leakage From DEVICE?

Of the 795 reports, 9 (1.1%) required hospitalization.

Is Device leakage Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 795 reports have been filed with the FAERS database.

What Other Side Effects Does DEVICE Cause?

Blood glucose increased (2,114) Device issue (1,417) Product use issue (1,076) Intercepted product preparation error (1,033) Wrong technique in product usage process (935) Injection site pain (751) Syringe issue (634) Product quality issue (567) Drug ineffective (488) Dyspnoea (482)

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) GUSELKUMAB (712) ABATACEPT (671)

Which DEVICE Alternatives Have Lower Device leakage Risk?

DEVICE vs DEXAMETHASONE DEVICE vs DEXAMETHASONE\DEXAMETHASONE DEVICE vs DEXAMETHASONE\NEOMYCIN DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B DEVICE vs DEXAMETHASONE\TOBRAMYCIN

Related Pages

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