Does EXENATIDE Cause Product dose omission issue? 1,053 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,053 reports of Product dose omission issue have been filed in association with EXENATIDE (Exenatide). This represents 3.4% of all adverse event reports for EXENATIDE.
1,053
Reports of Product dose omission issue with EXENATIDE
3.4%
of all EXENATIDE reports
1
Deaths
51
Hospitalizations
How Dangerous Is Product dose omission issue From EXENATIDE?
Of the 1,053 reports, 1 (0.1%) resulted in death, 51 (4.8%) required hospitalization, and 5 (0.5%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EXENATIDE. However, 1,053 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 dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which EXENATIDE Alternatives Have Lower Product dose omission issue Risk?
EXENATIDE vs EXFORGE
EXENATIDE vs EXJADE
EXENATIDE vs EXTAVIA
EXENATIDE vs EXTRANEAL
EXENATIDE vs EYLEA