Does EXENATIDE Cause Device leakage? 5,115 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5,115 reports of Device leakage have been filed in association with EXENATIDE (Exenatide). This represents 16.3% of all adverse event reports for EXENATIDE.
5,115
Reports of Device leakage with EXENATIDE
16.3%
of all EXENATIDE reports
2
Deaths
138
Hospitalizations
How Dangerous Is Device leakage From EXENATIDE?
Of the 5,115 reports, 2 (0.0%) resulted in death, 138 (2.7%) required hospitalization, and 8 (0.2%) were considered life-threatening.
Is Device leakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EXENATIDE. However, 5,115 reports have been filed with the FAERS database.
What Other Side Effects Does EXENATIDE Cause?
Injection site haemorrhage (5,527)
Injection site pain (4,577)
Injection site mass (3,506)
Blood glucose increased (3,363)
Incorrect dose administered by device (3,332)
Device malfunction (3,273)
Wrong technique in device usage process (3,255)
Device issue (2,862)
Weight decreased (2,702)
Injection site extravasation (2,320)
What Other Drugs Cause Device leakage?
SOMATROPIN (9,113)
LEUPROLIDE (5,861)
PEGFILGRASTIM (1,380)
ALBIGLUTIDE (1,195)
SECUKINUMAB (910)
RISPERIDONE (878)
TREPROSTINIL (874)
DEVICE (795)
GUSELKUMAB (712)
ABATACEPT (671)
Which EXENATIDE Alternatives Have Lower Device leakage Risk?
EXENATIDE vs EXFORGE
EXENATIDE vs EXJADE
EXENATIDE vs EXTAVIA
EXENATIDE vs EXTRANEAL
EXENATIDE vs EYLEA