Does EXENATIDE Cause Device failure? 187 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 187 reports of Device failure have been filed in association with EXENATIDE (Exenatide). This represents 0.6% of all adverse event reports for EXENATIDE.
187
Reports of Device failure with EXENATIDE
0.6%
of all EXENATIDE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Device failure From EXENATIDE?
Of the 187 reports, 3 (1.6%) required hospitalization, and 2 (1.1%) were considered life-threatening.
Is Device failure Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EXENATIDE. However, 187 reports have been filed with the FAERS database.
What Other Side Effects Does EXENATIDE Cause?
Injection site haemorrhage (5,527)
Device leakage (5,115)
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)
What Other Drugs Cause Device failure?
EPINEPHRINE (1,344)
SOMATROPIN (1,141)
PEGFILGRASTIM (829)
TREPROSTINIL (713)
BACLOFEN (691)
BUDESONIDE\FORMOTEROL (686)
ETANERCEPT (576)
GOLIMUMAB (487)
LEVONORGESTREL (332)
ACLIDINIUM (304)
Which EXENATIDE Alternatives Have Lower Device failure Risk?
EXENATIDE vs EXFORGE
EXENATIDE vs EXJADE
EXENATIDE vs EXTAVIA
EXENATIDE vs EXTRANEAL
EXENATIDE vs EYLEA