Does EXENATIDE Cause Poor quality device used? 18 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Poor quality device used have been filed in association with EXENATIDE (Exenatide). This represents 0.1% of all adverse event reports for EXENATIDE.
18
Reports of Poor quality device used with EXENATIDE
0.1%
of all EXENATIDE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Poor quality device used From EXENATIDE?
Of the 18 reports.
Is Poor quality device used Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EXENATIDE. However, 18 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 Poor quality device used?
SOMATROPIN (3,162)
MOMETASONE FUROATE (2,159)
ALBUTEROL (1,251)
FORMOTEROL\MOMETASONE FUROATE (1,091)
MEDROXYPROGESTERONE (80)
ETHINYL ESTRADIOL\ETONOGESTREL (77)
FOLLITROPIN (58)
ETONOGESTREL (55)
ETANERCEPT (46)
ESTRADIOL (41)
Which EXENATIDE Alternatives Have Lower Poor quality device used Risk?
EXENATIDE vs EXFORGE
EXENATIDE vs EXJADE
EXENATIDE vs EXTAVIA
EXENATIDE vs EXTRANEAL
EXENATIDE vs EYLEA