Does EXENATIDE Cause Device malfunction? 3,273 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 3,273 reports of Device malfunction have been filed in association with EXENATIDE (Exenatide). This represents 10.5% of all adverse event reports for EXENATIDE.
3,273
Reports of Device malfunction with EXENATIDE
10.5%
of all EXENATIDE reports
6
Deaths
99
Hospitalizations
How Dangerous Is Device malfunction From EXENATIDE?
Of the 3,273 reports, 6 (0.2%) resulted in death, 99 (3.0%) required hospitalization, and 6 (0.2%) were considered life-threatening.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EXENATIDE. However, 3,273 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)
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 malfunction?
PEGFILGRASTIM (6,818)
BUDESONIDE\FORMOTEROL (2,771)
ABATACEPT (2,459)
SOMATROPIN (2,311)
GOLIMUMAB (2,293)
SECUKINUMAB (2,259)
ALBUTEROL (2,257)
GUSELKUMAB (1,410)
MOMETASONE FUROATE (1,332)
ACLIDINIUM (1,325)
Which EXENATIDE Alternatives Have Lower Device malfunction Risk?
EXENATIDE vs EXFORGE
EXENATIDE vs EXJADE
EXENATIDE vs EXTAVIA
EXENATIDE vs EXTRANEAL
EXENATIDE vs EYLEA