Does EXENATIDE Cause Product administration error? 89 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 89 reports of Product administration error have been filed in association with EXENATIDE (Exenatide). This represents 0.3% of all adverse event reports for EXENATIDE.
89
Reports of Product administration error with EXENATIDE
0.3%
of all EXENATIDE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product administration error From EXENATIDE?
Of the 89 reports, 3 (3.4%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EXENATIDE. However, 89 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 administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which EXENATIDE Alternatives Have Lower Product administration error Risk?
EXENATIDE vs EXFORGE
EXENATIDE vs EXJADE
EXENATIDE vs EXTAVIA
EXENATIDE vs EXTRANEAL
EXENATIDE vs EYLEA