Does EXENATIDE Cause Device use issue? 992 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 992 reports of Device use issue have been filed in association with EXENATIDE (Exenatide). This represents 3.2% of all adverse event reports for EXENATIDE.
992
Reports of Device use issue with EXENATIDE
3.2%
of all EXENATIDE reports
0
Deaths
16
Hospitalizations
How Dangerous Is Device use issue From EXENATIDE?
Of the 992 reports, 16 (1.6%) required hospitalization, and 3 (0.3%) were considered life-threatening.
Is Device use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EXENATIDE. However, 992 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 use issue?
SOMATROPIN (2,571)
LEVONORGESTREL (2,489)
COPPER (1,318)
BUDESONIDE\FORMOTEROL (1,236)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (976)
DUPILUMAB (528)
ALIROCUMAB (471)
INSULIN GLARGINE (469)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (459)
LEVODOPA (443)
Which EXENATIDE Alternatives Have Lower Device use issue Risk?
EXENATIDE vs EXFORGE
EXENATIDE vs EXJADE
EXENATIDE vs EXTAVIA
EXENATIDE vs EXTRANEAL
EXENATIDE vs EYLEA