Does EXENATIDE Cause Device delivery system issue? 1,533 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,533 reports of Device delivery system issue have been filed in association with EXENATIDE (Exenatide). This represents 4.9% of all adverse event reports for EXENATIDE.
1,533
Reports of Device delivery system issue with EXENATIDE
4.9%
of all EXENATIDE reports
1
Deaths
27
Hospitalizations
How Dangerous Is Device delivery system issue From EXENATIDE?
Of the 1,533 reports, 1 (0.1%) resulted in death, 27 (1.8%) required hospitalization, and 3 (0.2%) were considered life-threatening.
Is Device delivery system issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EXENATIDE. However, 1,533 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 delivery system issue?
ALBUTEROL (9,509)
SOMATROPIN (1,848)
BUDESONIDE\FORMOTEROL (1,260)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (1,181)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (523)
LEVALBUTEROL (459)
MOMETASONE FUROATE\OLOPATADINE (347)
ABATACEPT (342)
PEGFILGRASTIM (323)
ALBUTEROL\BUDESONIDE (244)
Which EXENATIDE Alternatives Have Lower Device delivery system issue Risk?
EXENATIDE vs EXFORGE
EXENATIDE vs EXJADE
EXENATIDE vs EXTAVIA
EXENATIDE vs EXTRANEAL
EXENATIDE vs EYLEA