Does EXENATIDE Cause Product use issue? 725 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 725 reports of Product use issue have been filed in association with EXENATIDE (Exenatide). This represents 2.3% of all adverse event reports for EXENATIDE.
725
Reports of Product use issue with EXENATIDE
2.3%
of all EXENATIDE reports
1
Deaths
42
Hospitalizations
How Dangerous Is Product use issue From EXENATIDE?
Of the 725 reports, 1 (0.1%) resulted in death, 42 (5.8%) required hospitalization, and 3 (0.4%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EXENATIDE. However, 725 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 Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which EXENATIDE Alternatives Have Lower Product use issue Risk?
EXENATIDE vs EXFORGE
EXENATIDE vs EXJADE
EXENATIDE vs EXTAVIA
EXENATIDE vs EXTRANEAL
EXENATIDE vs EYLEA